Quality Assurance (QA) jobs involve the systematic monitoring and evaluation of the various aspects of a project, service, or facility to ensure that standards of quality are being met. The primary goal is to identify defects and issues before the product reaches the customer, thereby ensuring customer satisfaction and maintaining the reputation of an organization. QA roles often require attention to detail, strong problem-solving skills, and a good understanding of industry-specific regulations and standards. These jobs can vary widely, from software testing to food safety inspection, but they universally function as a critical checkpoint in the production and delivery process of goods or services.
Quality Assurance (QA) jobs involve ensuring that products and services meet certain standards of quality before they reach the consumer. Those in QA roles are responsible for developing and implementing testing processes, inspecting products for defects and non-compliance, and analyzing quality data to drive improvements. A key characteristic of QA positions is the focus on preventing errors rather than just correcting them, which necessitates a proactive approach and attention to detail. Additionally, QA professionals often collaborate closely with production teams to foster a culture of quality throughout an organization.
Quality Assurance (QA) jobs involve ensuring that products or services meet specific standards and satisfy customer expectations. Professionals in this field focus on systematic processes and preventative measures during production or development to prevent mistakes and defects. QA roles typically require keen attention to detail, problem-solving skills, and knowledge of industry standards. They may encompass various tasks, such as developing quality assurance plans, conducting tests, and analyzing data to improve quality and reliability. QA jobs contribute significantly to a company's reputation by guaranteeing product consistency and safety.
provide confidence in delivered software. Special attention is placed on documentation as a support tool for scope, test results, and feature acceptance. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world.
Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually
evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Essential activities of this position Run exploratory tests and writes new test plans.
Document features through testplans, manages test cases as a library. Provide new feature feedback to developers and product owners. Contributeto regression test definition andexecution. Advocate for end users. Perform verification and validation of large pools of data. Decode implied requirements. Strong Communication and Collaboration skills, written and verbal. Ability to ensure testing traceability and create test reports. Partner and collaborate
as part of the development team to deliver high-quality software which.Solves a problem Is easy to use Is reliable Qualifications of this position 2-8 years of experience in software testing or relevant work experience.
Tools include: Postman, Azure Dev Ops, BDDUnderstand human interaction with technology. Maintains a Completion-focused attitude and attentive to details. Ability to think in the abstract and see how small details fit into the bigger picture. Bonus Points for Experience in Strong IT skills Java + Selenium Roboticsshop operations or Healthcare Work environment and physical demands of this position The characteristics described below are representative of those encountered while performing the essential functions of this position.
When properly requested and when feasible (without undue hardship to the organization), reasonable accommodations will be made to enable individuals with disabilities to perform essential job functions. Work will primarily be in the office setting with limited opportunities to be exposed to adverse environmental conditions. Work will be primarily working with fingers by picking, pinching, typing and grasping often with repetitive motion. Must have visual acuity for viewing a computer screen, the ability to talk, hear and sit for extended periods of time.
Must be able to carry, lift and push/pull up to 5 pounds frequently and up to 30 pounds occasionally. Additional physical duties may be required as necessary. While COVID-19 precautions are in effect, this role requires use of face masks/face coverings while working in our facilities. Supervisory/Management position No Advancement opportunities: Senior QA Analyst Automation Engineer Product Owner For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required.
Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary The Parata QA Analyst focuses on verifying the solution provided by Development matches the needs described by Product. This person advocates for the user during design and testing by regularly questioning the purpose and effectiveness of features. Through this frequent inspection and feedback, you will provide confidence in delivered software.
Special attention is placed on documentation as a support tool for scope, test results, and feature acceptance. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Essential activities of this position Run exploratory tests and writes new test plans. Document features through testplans, manages test cases as a library. Provide new feature feedback to developers and product owners. Contributeto regression test definition andexecution. Advocate for end users. Perform verification and validation of large pools of data.
Decode implied requirements. Strong Communication and Collaboration skills, written and verbal. Ability to ensure testing traceability and create test reports. Partner and collaborate as part of the development team to deliver high-quality software which.Solves a problem Is easy to use Is reliable Qualifications of this position 2-8 years of experience in software testing or relevant work experience. Tools include: Postman, Azure Dev Ops, BDDUnderstand human interaction with technology. Maintains a Completion-focused attitude and attentive to details. Ability to think in the abstract and see how small details fit into the bigger picture.
Bonus Points for Experience in Strong IT skills Java + Selenium Roboticsshop operations or Healthcare Work environment and physical demands of this position The characteristics described below are representative of those encountered while performing the essential functions of this position. When properly requested and when feasible (without undue hardship to the organization), reasonable accommodations will be made to enable individuals with disabilities to perform essential job functions. Work will primarily be in the office setting with limited opportunities to be exposed to adverse environmental conditions.
Work will be primarily working with fingers by picking, pinching, typing and grasping often with repetitive motion. Must have visual acuity for viewing a computer screen, the ability to talk, hear and sit for extended periods of time. Must be able to carry, lift and push/pull up to 5 pounds frequently and up to 30 pounds occasionally. Additional physical duties may be required as necessary. While COVID-19 precautions are in effect, this role requires use of face masks/face coverings while working in our facilities.
Supervisory/Management position No Advancement opportunities: Senior QA Analyst Automation Engineer Product Owner For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work.
It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer.
We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job PDN-9aebe04b-0ac8-4314-bc5b-5fccf5594b52
of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self.
Become a maker of possible with us. Excited to grow your career? We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply! Our people make all the difference
in our success. The Staff Quality Engineer is a key member of the New Products Development Team and is responsible for Quality Assurance related R&D activities from research through product launch.
This position ensures that quality engineering principles are applied to new product development and sustaining engineering projects. You will be Accountable for the Following: Responsible for being the core team quality representative for design control projects - new product development as well as sustaining efforts. Manage all quality aspects of the design control process: quality planning; verification and validation planning and execution; risk management; regulatory and compliance support.
Provide clarification and guidance to teams on overall quality system with emphasis in design controls.
Work closely with Program Managers to ensure design deliverables are met and can be released to limited commercial and/or general release. Works together with Quality Engineers to ensure effective verification of design specifications and requirements. Monitors and ensures compliance with company policies and procedures (e. pliance with FDA, BSI, CSA, etc. ). Identifies areas requiring quality improvement and initiates and follows through plans of action necessary for implementation. Active participant in the development of product requirement, product system hazard analysis and design reviews.
Proactively engage partners to drive consensus and resolve issues in a timely fashion. Provide statistical support and expertise and analytical problem solving for product development and manufacturing Ensure product technical files and Design History Files are complete and auditable. Drive continuous improvement efforts, through facilitating, leading, and collaborating with cross functional teams What Success Looks Like in This Role: Demonstrates strong knowledge of quality engineering policies, principles and best practices Understanding of regulatory and international standards requirements including 21 CFR 210, 211, ISO 13485, ISO 14971 to support work with little or no supervision Applies comprehensive knowledge of software quality concepts within the software development lifecycle Knowledge of product development processes Represents Quality organization on cross-functional product development Core Team(s)Identify risks and proactively work with the program team to document risks and help to develop and ensure mitigation plans are in place Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)Applies knowledge and skills to a wide range of standard and non-standard situations Works independently with minimal guidance Usually determines own work priorities Acts as a resource for colleagues with less experience Basic Qualifications: Bachelor's degree in Engineering (or relevant STEM field) and minimum 8 years' experience with emphasis on R&D development, Quality Engineering and Design Control Experience with software and hardware development within a regulated environment is preferred.
Thorough understanding of the risk management and quality by design is preferred Attentiveness to details with strong organizational skills Ability to work proactively and independently Ability to multi-task and efficient in time management Excellent verbal communication and interpersonal skills with the ability to work in a team environment Proficiency in Excel, Word, and other desktop/general business systems Quality Engineering Certification (ASQ) or equivalent (preferred)Applicants must be authorized to work for ANY employer in the US.
We are unable to sponsor or take over sponsorship of employment visa at this time. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19.
In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN#SWE Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Excited to grow your career? We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions.
If you think the open position you see is right for you, we encourage you to apply! Our people make all the difference in our success. The Staff Quality Engineer is a key member of the New Products Development Team and is responsible for Quality Assurance related R&D activities from research through product launch. This position ensures that quality engineering principles are applied to new product development and sustaining engineering projects. You will be Accountable for the Following: Responsible for being the core team quality representative for design control projects - new product development as well as sustaining efforts.
Manage all quality aspects of the design control process: quality planning; verification and validation planning and execution; risk management; regulatory and compliance support. Provide clarification and guidance to teams on overall quality system with emphasis in design controls. Work closely with Program Managers to ensure design deliverables are met and can be released to limited commercial and/or general release. Works together with Quality Engineers to ensure effective verification of design specifications and requirements.
Monitors and ensures compliance with company policies and procedures (e. pliance with FDA, BSI, CSA, etc. ). Identifies areas requiring quality improvement and initiates and follows through plans of action necessary for implementation. Active participant in the development of product requirement, product system hazard analysis and design reviews. Proactively engage partners to drive consensus and resolve issues in a timely fashion. Provide statistical support and expertise and analytical problem solving for product development and manufacturing Ensure product technical files and Design History Files are complete and auditable.
Drive continuous improvement efforts, through facilitating, leading, and collaborating with cross functional teams What Success Looks Like in This Role: Demonstrates strong knowledge of quality engineering policies, principles and best practices Understanding of regulatory and international standards requirements including 21 CFR 210, 211, ISO 13485, ISO 14971 to support work with little or no supervision Applies comprehensive knowledge of software quality concepts within the software development lifecycle Knowledge of product development processes Represents Quality organization on cross-functional product development Core Team(s)Identify risks and proactively work with the program team to document risks and help to develop and ensure mitigation plans are in place Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)Applies knowledge and skills to a wide range of standard and non-standard situations Works independently with minimal guidance Usually determines own work priorities Acts as a resource for colleagues with less experience Basic Qualifications: Bachelor's degree in Engineering (or relevant STEM field) and minimum 8 years' experience with emphasis on R&D development, Quality Engineering and Design Control Experience with software and hardware development within a regulated environment is preferred.
Thorough understanding of the risk management and quality by design is preferred Attentiveness to details with strong organizational skills Ability to work proactively and independently Ability to multi-task and efficient in time management Excellent verbal communication and interpersonal skills with the ability to work in a team environment Proficiency in Excel, Word, and other desktop/general business systems Quality Engineering Certification (ASQ) or equivalent (preferred)Applicants must be authorized to work for ANY employer in the US.
We are unable to sponsor or take over sponsorship of employment visa at this time. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive.
And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN#SWE Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job PDN-9ae1d1d4-be9b-4576-9da5-227b73a266e9
of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self.
Become a maker of possible with us. Excited to grow your career? We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply! Our people make all the difference
in our success. We are the makers of possible. BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat.
It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. The
Senior Software Quality Engineer is a key member of the New Products Development Team and is responsible for QA-related R&D activities from research through product launch.
This position ensures that quality engineering principles are applied to new product development and sustaining engineering projects. You will be Accountable for the Following: Responsible for being the primary quality representative for design control projects - new product development as well as sustaining efforts. Responsible for review and/or approval of design history file documentation in support of design controls. Manage all quality aspects of the design control process: quality planning; verification and validation planning and execution; risk management; regulatory and compliance support.
Provide clarification and guidance to teams on overall quality system with emphasis in design controls. Work closely with Program Managers to ensure design deliverables are met and can be released to limited commercial and/or general release. Works together with other Quality Engineers to ensure effective verification of design specifications and requirements. Monitors and ensures compliance with company policies and international standards. Reviews and approves Change Orders and/or Electronic Release Authorizations for new releases or design enhancements.
Identifies areas requiring quality improvement, initiates and follows through on plans of action necessary for implementation. Active participant in the development of product requirements, product system hazard analysis and design reviews. Work closely with Product Management to ensure effective validation of user needs. Ensure product technical files and Design History Files are complete and auditable. Drive continuous improvement efforts, through facilitating, leading, and collaborating with cross-functional teams.
What Success Looks Like in This Role: Demonstrates intermediate knowledge of quality engineering policies, principles and best practices Applies intermediate understanding of regulatory requirements (c GMP, FDA, ISO, etc. ) to support work with little or no supervision Applies comprehensive knowledge of software quality concepts within the software development lifecycle Comprehensive knowledge in software development, including knowledge of software engineering, as well as test processes and methods Able to pull reports (queries), interpret trends and make recommendations for improvement to existing processes and tools Uses comprehensive expertise to help improve and streamline the software quality or development process Represents Quality organization on cross-functional product development Core Team(s) Review complex test cases/scripts and interprets/analyzes results to report, communicate, and work through issues with software engineers Considered expert in critical areas of the system and influences project test solutions Can apply understanding of the inter-workings of the application code under test Participates in design reviews Applies software engineering knowledge to tasking (e.
g. code and detailed design reviews, low-level white box testing, etc. ) Applies knowledge and skills to a wide range of standard and non-standard situations Basic Qualifications: Bachelor's degree in Engineering (or relevant field) and minimum 5 years' experience with emphasis on Software Quality Assurance and Design Control Thorough understanding of the risk management and quality by design Attentiveness to details with strong organizational skills Ability to work proactively and independently Ability to multi-task and efficient in time management Excellent verbal communication and interpersonal skills with the ability to work in a team environment Experience in software development and experience within a regulated environment is preferred applicants must be authorized to work for ANY employer in the US.
We are unable to sponsor or take over sponsorship of employment visa at this time. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be phenomenal, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health.
At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN#SWE Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Excited to grow your career? We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply! Our people make all the difference in our success.
We are the makers of possible. BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self.
Become a maker of possible with us. The Senior Software Quality Engineer is a key member of the New Products Development Team and is responsible for QA-related R&D activities from research through product launch. This position ensures that quality engineering principles are applied to new product development and sustaining engineering projects. You will be Accountable for the Following: Responsible for being the primary quality representative for design control projects - new product development as well as sustaining efforts. Responsible for review and/or approval of design history file documentation in support of design controls.
Manage all quality aspects of the design control process: quality planning; verification and validation planning and execution; risk management; regulatory and compliance support. Provide clarification and guidance to teams on overall quality system with emphasis in design controls. Work closely with Program Managers to ensure design deliverables are met and can be released to limited commercial and/or general release. Works together with other Quality Engineers to ensure effective verification of design specifications and requirements.
Monitors and ensures compliance with company policies and international standards. Reviews and approves Change Orders and/or Electronic Release Authorizations for new releases or design enhancements. Identifies areas requiring quality improvement, initiates and follows through on plans of action necessary for implementation. Active participant in the development of product requirements, product system hazard analysis and design reviews. Work closely with Product Management to ensure effective validation of user needs. Ensure product technical files and Design History Files are complete and auditable.
Drive continuous improvement efforts, through facilitating, leading, and collaborating with cross-functional teams. What Success Looks Like in This Role: Demonstrates intermediate knowledge of quality engineering policies, principles and best practices Applies intermediate understanding of regulatory requirements (c GMP, FDA, ISO, etc. ) to support work with little or no supervision Applies comprehensive knowledge of software quality concepts within the software development lifecycle Comprehensive knowledge in software development, including knowledge of software engineering, as well as test processes and methods Able to pull reports (queries), interpret trends and make recommendations for improvement to existing processes and tools Uses comprehensive expertise to help improve and streamline the software quality or development process Represents Quality organization on cross-functional product development Core Team(s) Review complex test cases/scripts and interprets/analyzes results to report, communicate, and work through issues with software engineers Considered expert in critical areas of the system and influences project test solutions Can apply understanding of the inter-workings of the application code under test Participates in design reviews Applies software engineering knowledge to tasking (e.
g. code and detailed design reviews, low-level white box testing, etc. ) Applies knowledge and skills to a wide range of standard and non-standard situations Basic Qualifications: Bachelor's degree in Engineering (or relevant field) and minimum 5 years' experience with emphasis on Software Quality Assurance and Design Control Thorough understanding of the risk management and quality by design Attentiveness to details with strong organizational skills Ability to work proactively and independently Ability to multi-task and efficient in time management Excellent verbal communication and interpersonal skills with the ability to work in a team environment Experience in software development and experience within a regulated environment is preferred applicants must be authorized to work for ANY employer in the US.
We are unable to sponsor or take over sponsorship of employment visa at this time. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19.
In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be phenomenal, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN#SWE Primary Work Location USA NC - Durham - Roche Drive Additional Locations Work Shift Apply Save Job PDN-9ae1d1d4-f53d-4c3c-acd6-ec24caa1ed10
be expected to review and authorize testing results, partner in day-to-day lab scheduling, provide leadership in lean lab initiatives, have a strong comprehension of Labware LIMS, SAP, handle Quality Notification authoring and provide audit support. Position Responsibilities General Ability to work independently and as a member of a team.
Contributes to the performance and results of the Sample Control team. Receive, document, and prepare samples for further testing or shipment. Adapts plans and priorities to address resource and operational challenges. Decisions are guided by policies, procedures and/or business plans. Requires knowledge and experience in own discipline; still acquiring
higher-level knowledge and skills. Builds knowledge of the company, processes and clients and/or customers Analyzes possible solutions using standard procedures.
Receives a moderate level of guidance and direction. Conduct retains maintenance activities, sampling, and testing as per described procedures. Applies team effectiveness skills, listening and integrating diverse perspectives from across the work group; contributes and adds value to the achievement of team goals. Build relationships to work in a highly functioning diverse team environment. Functional Expertise Basic conceptual knowledge and practices associated with document review as it relates to bulk, raw materials, and general
incoming components. Conduct necessary SAP transactions to indicate task completions or stock status updates to support batch disposition decisions.
Provide support to Vendor Quality Management system. Lead Supplier Qualification and Reduced Testing initiatives Comprehends and applies regulatory and compliance requirements relative to their role. Comprehends the fundamental business drivers for the company and uses this knowledge in own work. Basic conceptual knowledge and practices associated with inspection of incoming components and materials utilized in manufacturing in accordance with component specifications and procedures. Utilizing component specifications to conduct visual inspections, dimensional verifications, document reviews, and other tasks related to quality control to ensure materials meet quality standards as applicable.
Document results of inspection onto inspection record and global laboratory information system Meticulous attention to detail and possess good organizational skills. Assist in investigations, which includes interactions with vendors or our Company internal teams to resolve issues associated with incoming components. Development of metrics and process improvements for disposition prioritization and lead time reduction Participate in process improvement or learning events, as guided or approved by Quality management.
Author, review, and approve Standard Operating Procedures (SOPs)Participate in GEMBAs and safety walkthroughs. Direct support of regulatory inspections and audits Replies to standard requests from clients and/or customers. Explains information and persuades others in straightforward situations. Problem Solving Identifies and solves a range of problems in straightforward situations; analyzes possible solutions and backsses each using standard procedures. Supports resolution of technical and operational problems through partnership with peers Applies appropriate risk management while adhering to Current Good Manufacturing Practice (c GMP) requirements.
Makes decisions guided by policies and procedures that impact the team's ability to meet performance objectives. Consults on an as-needed basis with next-level manager on more complex decisions and/or issues that impact other units with interrelated processes. Physical Requirements Ability to sit, stand and move within workspace for extended period. Ability to lift fifty (50) pounds. Education Bachelor's degree in biology, Chemistry, or other related areas of study.
Required Experience and Skills c GMP within a medical operation complying with both domestic and international regulations. Minimum two years in medical operations, technical services, and/or quality operations with at least one year in a quality function Incoming release work experience SAP knowledge Preferred Experience and Skills Quality Control and/or Quality Assurance with Track Wise, or Global Laboratory Information Management System Inspecting components Microsoft Office Suite ANSI sampling plans and how to apply them. Responding to regulatory questions with multiple agencies (FDA, EMA, JNDA, )Assay development, validation, or technical transfers Knowledgeable in the use of GLIMs Knowledge of CFR, and Compendia testing specific to the medical industry Regulatory agency audits and/or regulatory filings NOTICE FOR INTERNAL APPLICANTS In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package.
To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor. VETJOBS #EBRG Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders (for example, a requirement to be vaccinated against COVID-19 in order to access a facility or meet with stakeholders).
Please understand that, as permitted by applicable law, if you have not been vaccinated against COVID-19 and an essential function of your job is to call on external stakeholders who require vaccination to enter their premises or engage in face-to-face meetings, then your employment may pose an undue burden to business operations, in which case you may not be offered employment, or your employment could be terminated. Please also note that, where permitted by applicable law, the Company reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature of the role presents an increased risk of disease transmission.
Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, interaction, interactionual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U. S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement Pay Transparency Nondiscrimination We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.
The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U. S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U. S. will be working a Hybrid work consisting of three total days on-site per week, generally Tuesday, Wednesday and either Monday or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.
This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely.
Please note, this Hybrid work model guidance also does not apply to roles that have been designated as " remote" Search Firm Representatives Please Read Carefully Merck & Co. Inc. Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.
No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: On-Site Shift: 1st - Day Valid Driving License: No Hazardous Material(s): Lab environment Requisition ID: R272223PDN-9ad5c250-f4e9-4acf-b45b-c357bf74fc56
and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. Position Responsibilities: Conducts testing and associated tasks without errors per applicable SOPs and protocols Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written Works in a team environment to accomplish departmental goals Develops expertise in assigned assays/techniques Assist in the maintenance of the lab including routine housekeeping activities and waste management Maintenance of lab equipment May be required
to perform off shift work as required to support operations and perform other duties as assigned Education Minimum Requirement: B.
S. degree in science field, preferably biology, biochemistry, biotechnology or Biomedical Sciences.
Required Experience and Skills: A minimum of 1 year experience working in a laboratory setting. Must be able to discriminate colors for characteristics tests or related assays. Demonstrated interpersonal, technical aptitude, and problem solving skills. Experience in using pipettes (single channel, Multichannel)Experience with the p H meter instrument and analytical balances. Ability to perform basic scientific math, must have strong computer skills and
Proficiencywith MS Office applications required. Must be flexible and able to manage multiple assigned tasks.
Must have attention to details and good documentation skill. Communicates well with co-workers and superiors Ability to analyze data and write up results Able to lift 25 lbs. Preferred Experience and Skills: Prior experience in a GMP Quality Control laboratory strongly preferred Cell culturemaintenance and aseptic techniques experience Familiar with cell-based assays Learn new methods and expand capabilities within the laboratory Knowledge of safety guidelines in a laboratory environment Be sharp, self-motivated, and able to thrive in a fast-paced dynamic environment.
NOTICE FOR INTERNAL APPLICANTS In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions. If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package.
To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor. VETJOBS #EBRG Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders (for example, a requirement to be vaccinated against COVID-19 in order to access a facility or meet with stakeholders). Please understand that, as permitted by applicable law, if you have not been vaccinated against COVID-19 and an essential function of your job is to call on external stakeholders who require vaccination to enter their premises or engage in face-to-face meetings, then your employment may pose an undue burden to business operations, in which case you may not be offered employment, or your employment could be terminated.
Please also note that, where permitted by applicable law, the Company reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature of the role presents an increased risk of disease transmission.
Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, interaction, interactionual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics.
For more information about personal rights under the U. S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement Pay Transparency Nondiscrimination We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts U. S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U. S. will be working a Hybrid work consisting of three total days on-site per week, generally Tuesday, Wednesday and either Monday or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence. This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely.
Please note, this Hybrid work model guidance also does not apply to roles that have been designated as " remote" Search Firm Representatives Please Read Carefully Merck & Co.
Inc. Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific.
Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: On-Site Shift: Not Indicated Valid Driving License: No Hazardous Material(s): Cleaning supplies Requisition ID: R271153PDN-9ad3c00f-a4a1-41db-9844-7691b80f73cb
and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of Ph D chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter the marketplace.
THE POSITION We are seeking an experienced Quality Assurance Label Associate/ Specialist (dependent upon experience) who will be responsible for managing label control, reconciliation, and issuance programs as part of our expanding Quality Management System (" QMS" ) which includes: industry,
regulatory, and c GMP manufacturing compliance and certification programs; in-house and third party product quality testing throughout the manufacturing process; and comprehensive SOP's and employee compliance training.
The Quality Assurance Label Associate/ Specialist (dependent upon experience) must bring a high level of energy and possess the leadership and flexibility to adapt to the evolving and infant regulatory landscape of the industry. RESPONSIBILITIES Conducts inspections of incoming retail labels Implementation of a label repository and the authority on label version control Maintains physical inventory and updates documentation of the usage of retail labels Ensures the label
storage locations are maintained in a secure fashion Responsible for label issuance to Finished Goods Manufacturing and Label Reconciliation during and post production Conducts obsolete label and other customer branded material destruction and maintains records accordingly Performs verification that the components listed in the Bill of Materials are correct and compatible with each other and the manufacturing equipment Gathers routine samples from manufacturing areas, performs the required analysis, and records and reports data in a timely manner Coordinate with department managers to develop, write, review and approve SOPs for the entire operation, from through finished product shipping and ensure SOPs are compliant across multiple regulatory frameworks.
Ensure finished products meet labeling standards for hemp including compliance with FDA regulations for foods and dietary supplements, ingredients, limitations on health claims, disclaimers and warnings. General oversight of facility recordkeeping, following Good Documentation Practices Other tasks as necessary to meet business needs. EXPERIENCE HS or equivalent required BS or equivalent in the physical sciences preferred Suggest " At least one year minimum required experience in the food, dietary supplement or medical industry Experience in the cannabis industry preferred but not required.
Strong knowledge of c GMP regulations and auditing techniques. Solid understanding of Quality Control and Quality Assurance c GMP requirements in FDA regulated environments preferred. High level of interpersonal skills, strong leadership abilities, organizational and time management skills. Excellent communicator. Ability to work independently and meet deadlines. OTHER DETAILS This is a full-time position based out of Roxboro, NC. Compensation commensurate with experience. Background and reference checks required.
PHYSICAL DEMANDS AND WORKING ENVIRONMENT: Must be able to lift, carry and balance up to 50 pounds While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and completing repetitive motions. Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending. Working in limited climate-controlled facilities and may experience extreme heat or cold Work with heavy fumes, plants, airborne particles and chemicals Must be comfortable working with and around heavy machinery May experience moderately high noise levels EQUAL EMPLOYMENT OPPORTUNITY STATEMENT Open Book Extracts is proud to be an equal opportunity employer.
We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
Quality Assurance (QA) Jobs encompass roles focused on ensuring that products or services meet established standards of quality, reliability, and performance. These positions typically involve identifying defects, designing test procedures, conducting tests, and making improvements. Key characteristics of QA jobs include attention to detail, a strong understanding of quality metrics, the ability to analyze data, and problem-solving skills. Individuals in QA roles work closely with development teams and are critical in maintaining customer satisfaction by preventing errors and enhancing the user experience.
Quality Assurance (QA) jobs involve ensuring that products or services meet specific standards and satisfy customer expectations. Professionals in this field focus on systematic processes and preventative measures during production or development to prevent mistakes and defects. QA roles typically require keen attention to detail, problem-solving skills, and knowledge of industry standards. They may encompass various tasks, such as developing quality assurance plans, conducting tests, and analyzing data to improve quality and reliability. QA jobs contribute significantly to a company's reputation by guaranteeing product consistency and safety.
Quality Assurance (QA) jobs involve the systematic monitoring and evaluation of the various aspects of a project, service, or facility to ensure that standards of quality are being met. The primary goal is to identify defects and issues before the product reaches the customer, thereby ensuring customer satisfaction and maintaining the reputation of an organization. QA roles often require attention to detail, strong problem-solving skills, and a good understanding of industry-specific regulations and standards. These jobs can vary widely, from software testing to food safety inspection, but they universally function as a critical checkpoint in the production and delivery process of goods or services.
Quality Assurance (QA) jobs entail roles focused on ensuring that products or services meet established standards and customer expectations. People in QA positions are responsible for designing testing processes, creating test plans, identifying defects, and preventing defects by examining the production process. They aim to enhance product reliability and actively work to maintain quality consistency. QA roles often require keen attention to detail, strong problem-solving skills, and an understanding of both product specifications and customer needs. QA is an integral part of product development and maintenance, bridging the gap between the manufacturing processes and the end users to ensure a satisfactory experience.
Quality Assurance (QA) jobs involve ensuring that products or services meet certain standards of quality before they reach the consumer. Individuals in QA roles are responsible for planning and implementing inspection processes, conducting tests, and analyzing the results to detect defects. They work to prevent errors and improve the overall quality of the final output. Key characteristics of QA jobs include attention to detail, a systematic approach to problem-solving, and a strong understanding of industry-specific regulations and quality standards. These professionals play a critical role in customer satisfaction and maintaining the reputation of a brand or company.
Quality Assurance (QA) Jobs encompass roles focused on ensuring that products or services meet established standards of quality, reliability, and performance. These positions typically involve identifying defects, designing test procedures, conducting tests, and making improvements. Key characteristics of QA jobs include attention to detail, a strong understanding of quality metrics, the ability to analyze data, and problem-solving skills. Individuals in QA roles work closely with development teams and are critical in maintaining customer satisfaction by preventing errors and enhancing the user experience.
