Client relationship & Business development Point of contact for TRIGO engineering services within site Ensures client satisfaction and building of solid relationships Ensures clear and transparent communication with internal and external customers Operations Responsible for engineering related costs and reports related to engineering missions to the customer Executes backssments/audits as per guidelines Monitors site engineering missions for proper documentation/information Makes sure engineering tools and equipment are up-to-date, with accurate information Represent plant operations on Production Team.
Design and implement LEAN practices (VSM, Continuous flow, Workplace organization
5S, Cycle time, takt time studies, Ergonomic, Define Waste, TPM program). Lead Kaizen events to find potential improvements. Develop and implement work instructions and train team members.
Design, redesign, and enhance work areas and layouts to be more ergo friendly, reduce repetitive motions and inefficient methods. Demonstrates commitment to reduce the risk of workplace accidents Must comply with local and company Health & Safety legislation, laws, and policies Work experience 1 - 3 years combined work experience in Quality, Industrial, Manufacturing Engineering and/or Operations; applying Industrial Engineering tools and methodologies Organization & management Demonstrate group and
individual presentation skills; actively participate in meetings, including high level customer, supplier, and business leader meetings Assists/monitors overall services provided within site on a daily basis Develops/trains site teams to assist with engineering service as related to missions Promotes workplace improvements and development Technical Ability to define problems, collect data, establish facts and draw valid conclusions Establishes methods for maximum utilization of materials, production facilities and/or personnel Other Any other duties as assigned Job Posted by Applicant Pro
services, we never forget the values that made us who we are as a company. We are a team. A family. A group of smart, talented, big-hearted individuals working together for the success of our customers and the growth of our communities. AND WE HONOR OUR COMMITMENTS What we do at Ortec is complicated at times.
Why we do what we do is not complicated: We want to make a difference for our customers and our communities around us. How we do what we do is also not complicated: everything starts with Integrity. WHY ORTEC? The foundation of Ortec is our talented, dedicated employees. Our commitment to delivering chemical manufacturing services with measurable quality has made us a trusted partner
to some of the most familiar names in business. Our success is drawn from the experience, energy and teamwork of our employees, who consistently deliver results by anticipating change and executing solutions with confidence and passion.
At Ortec, you'll be working with the latest technologies and tools, not to mention some of the industry's best and brightest minds. From the top down, this type of commitment and energy is radiated throughout the company. The result is a growing, dynamic, and rewarding place to work a company where we work as many and we win as one. You are a name, not a number! We offer an excellent benefit package, including: Medical, Dental, and Vision Insurance Company
Paid Short-Term Disability, Long-Term Disability and AD&D Annual Anniversary Cash Award On-Site Nurse Company Paid Employee Assistance Plan 401k with match Annual Anniversary Cash Award POSITION SUMMARY The QA Engineer - Validation job function is responsible for performing quality assurance tasks and activities with minimal guidance and supervision.
The emphasis for this position is on coordinating and supporting validation activities for the design, startup on equipment, and process validations for new and ongoing operations of the Ortec Piedmont facility. Technical duties include authoring and executing validation documents, defining validation strategy, reviewing and analyzing data, and incorporating continuous improvement into validation programs.
This individual will provide oversight of validation activities, lead the development and approval of validation documentation, risk backssments, work with project teams to determine which elements should be validated, and conduct impact backssments of proposed changes to systems. The QA Engineer role will also help support the implementation, coordination, and maintenance of Ortec's Quality Systems. ESSENTIAL FUNCTIONS Write, execute, summarize and lead validation projects in the following areas: facility design and validation (utility systems, environmental chambers, HVAC, for example) production and processing equipment process validations cleaning validations plant automation (PLC, SCADA and comparable systems) computer system validation.
Develop project timelines, maintain team schedules, and communicate progress to peers and senior management. Review and analyze test data. Obtain client approval for contracted validation projects and reports. Review and administer validation activities originating from process and equipment change control. As a subject matter expert, help develop responses to compliance audit findings (internal, client, and FDA).
Participate as member of audit support teams, representing validation programs, policies, and projects. Chair and coordinate FMEA teams, author FMEA reports and manage risk backssment activities for change control. Coordinate with Production, Quality, Maintenance, and other departments as needed to manage projects, implement production capacity increases, and validate process improvements. Define and implement global equipment and instrument maintenance and calibration program. Helps provide technical assistance to carry out problem analysis/complaint investigation where necessary, e.
g. quality events investigation and CAPAs Support audit readiness with understanding of FDA and ISO regulations and requirements. Maintain a safe, clean, and organized environment (5S) for all QA areas. Follow all SOPs and Safety Guidelines to ensure compliance with a c GMP environment and Safety Practices Any additional functions as assigned by the QA Manager Sustain, and uphold Ortec's Guiding Principles in all day-to-day actions EDUCATION Bachelor's degree in Business, English, or Science related field with 2+ years related experience Bachelor's degree in Business, English, or Science related field with 5 years related experience, preferred EXPERIENCE Preferred: Minimum 2+ years' experience in regulated manufacturing environment - chemical, medical or medical device with quality assurance responsibilities, specifically in technical writing Experience with regulatory inspections and writing validation protocols SKILLS & ABILITIES Demonstrated knowledge of validation principles Demonstrate knowledge of c GMP's including sections 211 and 820 Strong analytical and problem solving skills Proficient computer skills: Microsoft Outlook, Excel and Word.
Experience with Minitab desirable Excellent oral and written communication skills in English. Attention to details, ability to meet deadlines and work independently in fast-paced environment Ability to assertively interact with people at all levels of the organization Excellent technical writing skills Ability to think proactively Strong interpersonal skills, ability to be flexible and work well as a team player This job posting is not all inclusive, please see job description for details. Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, and background screenings.
Ortec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interactionual orientation, gender identity, national origin, veteran or disability status.
with the applicable welding procedure. Witness and supervise performance testing of outside agencies (as appropriate). Verify documentation of procedure qualification test results Document results of inspections Ensure requalification requirements are maintained Interpret drawings and documents Inspect and test welded joints of work currently in progress and work that is completed.
Inspect to ensure that dimensions, linings and coatings are in conformance with contract drawings and work order specifications. Perform inspection and testing of production weld samples, linings and coatings. Must be reliable and punctual. Must follow and enforce all safety standards. MINIMUM QUALIFICATIONS
Must be physically able to perform the essential functions of the job, with or without reasonable accommodations. Must be able to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
Must be able to write routine reports and correspondence. Must be able to speak effectively before managers or groups of employees. Must be able to add, subtract, multiply, and divide into all units of measure, using whole numbers, common fractions, and decimals. Must be able to compute ratio and percent and to interpret bar graphs. Must be able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram
form. Must be able to deal with problems involving several concrete variables in standardized situations.
Must be able to read, understand and interpret job drawings and specifications. Must be able to operate computer controlled hydrostatic test stand, including reading and interpreting console indicators and gauges, and using control console to conduct tests. Must have valid Certificate of Welding Inspector (AWS QC1 CWI). Must be able to manage a variety of tasks with conflicting priorities. PREFERRED QUALIFICATIONS Certification as ASNT-TC-1A Level II in Magnetic Particle (MT), Dye Penetrate (PT), and Ultrasonic Testing (UT) NDE a strong plus. Ability to work at heights with harness.
ESSENTIAL PHYSICAL FUNCTIONS The employee is regularly required to stand; walk; use hands or feel; and talk or hear. The employee is frequently required to stoop, kneel, crouch, or crawl. The employee is occasionally required to sit and reach with hands and arms. The employee must regularly lift and/ or move up to 25 pounds and occasionally lift and/or move up to 100 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision and ability to adjust focus.
of basic causes of customer complaints and returns, and participate in initiating corrective action. Maintain and update Visual Aids as needed. Provide technical training to quality department personnel. Create work instructions and operating procedures for new or changed processes, as well as rework instructions for non-standard operations.
Interpret standards, specifications, quality requirements, and quality planning for in-plant customer inspections. Contribute to preparation of control plans for each part to be used during production to maintain product quality. Assure that the quality level of the finished product meets the customer's specifications. Evaluate the performance of
Quality department personnel. Evaluate Quality department equipment and labor needs. Maintain accurate up-to-date inspection and test records as prescribed by the quality plan.
Participate in daily MRB disposition. QUALIFICATIONS: Minimum 10 years' experience in Quality Management in a multi-shift manufacturing environment. Experience with automotive customers is a must. Quality Management experience in aluminum die casting, metals manufacturing or injection molding serving the automotive industry is preferred. Bachelors Degree in Engineering, Business or related field is preferred. At a minimum, an Associates Degree is required. Excellent written and verbal communication skills. Thorough
understanding of IATF 16949 requirements, APQP, PPAP/FMEA, SPC, GRR, GDT, and Corrective/Preventive Action.
Computer literate with ability to work all Microsoft Office programs a must. Knowledge of and experience with CMMs a plus. Quality Manager, quality assurance, RCM Industries, Inc. Aallied Die Casting, Quality jobs, Automotive jobs, Quality engineer, Die Casting Quality Manager
and reporting of quality metrics including trend analysis, statistical analysis and statistical process control (SPC) as required. The function also includes root cause analysis in support of failure investigations and the ability to clearly communicate investigation findings and corrective actions to internal and external personnel including vendors, customers and customer quality inspectors.
The function includes direct supervision and training of quality assurance technicians and inspectors, and management of metrology and related standards for calibration. Key Responsibilities: Lead and coach quality department team to drive a high performing culture. Ability to evaluate current state
practices and analyze gathered data to identify opportunities for continuous improvement. Conducts periodic internal reviews or audits to ensure that compliance procedures are followed and investigate issues.
Responsible for scheduling and leading all customer and regulatory audits. Track corrective and preventive actions identified within audits, work with various units for completion and submit responses to agencies/customers when required. Conduct off-site audits of third parties and vendors with detailed report of findings. Prepares and submits weekly/monthly reports, prepares metrics and trends data to indentify and prioritize continuous improvement opportunities. Assists in developing
policies and procedures related to QA. Assist CAPA teams, and other project teams, in the development of action plans and implementation schedules, and the verification of completed actions.
Qualifications: Bachelor's Degree in business, Industrial Engineering and /or Mechanical Engineering. Minimum 5 years prior experience in Quality Assurance. Ability to effectively communicate and lead. Ability to multi-task and prioritize. Minimum 2 years directly related experience supporting compliance in a quality/compliance/function/applicable compliance field. Knowledge of QMS and CAPA related tools or systems is required. Experience with inspections and inspection readiness activities and audits is required.
Flexible and able to adapt to company growth and evolving responsibilities. Strong project management skills: MS Word, Excel, Power Point. Highly ethical, self-motivated and self-directed; works effectively independently as well as in a team environment. Communication Skills: Strong personal leadership with demonstrated competency interfacing with senior leaders is required. Listening, interpreting, and summarizing information. Clear and concise written communications- exceptional attention to detail. Strong organizational skills, with the ability to effectively prioritize and manage multiple projects and tasks, with attention to detail.
Strong interpersonal skills and the ability to assist personnel in a matrix organization, ability to proactively resolve issues in a diplomatic, flexible, and constructive manner. Equal Opportunity Employer We believe in the value of your unique identity, background, and experiences. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, age. marital status, genetic information, disability, interactionual orientation, gender identity, veteran status or any other status protected by the law.
analytical/microbial samples for in-house testing, disposition to contract laboratories for additional testing, retention, and destruction. (S)he will also prepare samples for both in-house and outside analyses and deliver samples to the Shipping Department as appropriate for shipment to contract laboratories, and will manage packing and transfer of retain samples to warehouse or off-site storage.
The QCI will conduct entry-level laboratory functions including but not limited to: Labeling and organization of all QC files, including the packing of documents for warehouse or off-site storage. (S)he will also assist QC Personnel and the QC with additional filing, scanning, or other clerical
duties as needed Restocking of lab supplies Daily performance check of balances in the QC Laboratory Physical testing such as: Color, Appearance, Odor determination, and Weight Variation.
Assist/perform in preparation of media, reagents and chemical solutions Keep the QC Laboratories supplied with clean glassware. (S)he will be proficient in the operation of the automated glassware dishwasher and the pipette washer and dryer, as well as with the procedures for the proper hand washing of laboratory hardware and supplies Perform all phases of material preparation and media sterilization for operation of autoclave Assist/perform membrane filtration of samples Perform daily checks of controlled
microorganisms Perform all phases of waste disposal to include removing garbage, samples, broth and plate disposal Ensure cleanliness of laboratory equipment, fume hoods/Bio Safety Cabinets (BSC) and laboratory areas The QCI will follow current c GMP protocols for the proper documentation of all procedures performed.
The QCI will provide input for the improvement or revision of QC Standard Operating Procedures (SOPs), Finished Product Specifications, and Raw Material Specifications, as appropriate. The QCI will maintain a safe working environment by following all laboratory safety guidelines and wearing Personal Protective Equipment (PPE) as appropriate.
Perform other assigned duties as may be required in meeting company objectives Regular attendance is required Communicate effectively with other departments within the organization and function within a team environment. Minimum Requirements : Ability to work in a fast-paced environment, attention to detail, effective interpersonal skills, and the ability to interact with all levels of personnel is required. Proficiency with Microsoft Word and Excel is preferred but is not required. Prior laboratory experience is preferred but is not required. Education and Experience : A high school diploma or General Educational Development (GED) credential is required for the QCI position.
Supervisory Responsibilities: None Job Posted by Applicant Pro
This position will work closely with the Project Manager for support at the project sites. Support project schedules and resources at the supplier Available for calls from any shifts Work as the key interface between suppliers and management On-site work at multiple project sites/suppliers Able to work a flexible schedule to include all shifts 1st, 2nd, and 3rd, and work longer shifts when needed.
Handle requests for information and data Maintain supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies. Communicate with Supervisors at client sites to supply requests Assist
HR with support and communication with employees Assist with the submission of weekly hours for all associates (employees/staffing) for customer invoicing and/or payroll processing Coordinate adjustments/changes required for customer invoicing and/or payroll Work with Staffing Partners to meet the required/needed headcount for projects Assisting HR to uphold company standards Train new hires and perform the task until headcount is met Training Matrix Conduct Audits as needed Conduct in-person onboarding sessions Perform other related duties as assigned by HR and Project Manager Minimum Qualifications (Knowledge, Skills, and Abilities) Minimum Qualifications (Knowledge, Skills, and Abilities)
High school diploma/GED.
2 years of Project support experience Good verbal and written communication skills.
Computer and data entry skills are preferred. Needs to be flexible for scheduling and available on an on-call basis. Attention to detail and accuracy Prioritizing, planning, and organizing Teamwork and customer service orientation Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Stand and walk for up to 12 hours a day Bend and squat repeatedly throughout the course of the day Perform repetitive work for multiple hours Able to stretch repeatedly throughout the shift Lift up to 40 pounds repeatedly Work in different climates, such as heat or cold, for an entire shift.
Recruiting exceptional talent is one of the key elements of RCM Industries, Inc. 's long-term success. We strive to find a diverse group of the most qualified and committed people, and offer them challenging opportunities that enable them to reach their full potential.
This position is located at Imperial Die Casting Co. in Liberty, SC. DUTIESThis position is responsible for the identification, evaluation and communication of quality related items associated with the various products manufactured in this facility. This includes but not limited to new product quality criteria in product launches, non-conforming product, non-standard operations, and any other production or quality items
found in the plant. This position is also responsible for customer contacts for quality and corrective and preventive actions. Develop and maintain plant-wide Control Plans and FMEAs Coordinate new project APQP with other departments and customers.
Develop other PPAP information for projects as required, including identification of critical characteristics, flow charts, gage R&Rs, inspection criteria and visual aids. Develop and maintain Statistical Process Control system to monitor critical and key product characteristics Active in the Internal Audit program to identify plant conformance/improvement opportunities and monitoring of action items Support plant-wide continuous improvement
programs Develop and maintain Visual Guides and product criteria inspection instructions Train QA and production personnel on quality criteria for products manufactured in plant.
Assist Quality and Production personnel in making quality judgments on defects during production runs. Review in-process non-conforming material and report on analysis; review and take action with production departments Liaison with customers to address problems and improvements to products Assist with the Corrective Action system, coordinate teams and submit responses QUALIFICATIONSAssociates Degree in Engineering or related field is desired. Three to five years manufacturing experience.
Metal casting or injection molding experience is a plus. Strong GD&T experience. Ability to read and interpret mechanical blueprints. Automotive customer experience is a plus.
Process Controls) Charts, and create solutions based off SPC data Use Quality Tools, such as 5-Why's, Ishikawa Diagrams, FEMA's and 8D's to the root cause problems and implement fixes Develop training modules for various data quality process sections. Identify areas requiring training and ensure gaps are completely filled within given time frame.
Collaborate with supervisors for performance enhancement of least performing personnel. Identify, estimate and correct deviations and defects in quality system process. Configure management required audits and perform OOBA (Out Of Box Audits) Inspect, monitor, record and report quality data for production and incoming Inspection activities to
assist in operations Prepare documents for RMA's (Return Material Authorizations) and Red Tag (Quarantine) defective materials Communicate to Purchasing Manager/vendors regarding Non-Conforming Materials Interact with Production/Finish and Engineering to help resolve quality issues.
Perform to direct by cognizant Quality management and Engineers. Qualifications Experience with quality control techniques such as Six Sigma Experience with measuring devices such as meters, gauges, computers, calipers, and other measuring instruments Four-Year Degree in Quality or related technical field, Engineering, Science, etc. Associates Degree with 3 years experience in a quality role or 5 years in
a manufacturing environment Equal Opportunity Employer We believe in the value of your unique identity, background, and experiences.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, age, marital status, genetic information, disability, interactionual orientation, gender identity, veteran status or any other status protected by the law.
Quality Assurance (QA) jobs involve ensuring that products, services, or processes meet established standards of quality through systematic activities and measures. These roles typically focus on preventing defects, identifying potential issues, and implementing solutions to maintain quality consistency. Key features of QA positions include rigorous testing, meticulous attention to detail, and a commitment to continuous improvement. QA professionals work across various industries, from software development to manufacturing, to safeguard customer satisfaction and comply with regulatory requirements.
also provides cost-effective commercial training and digital forensics services. Predicate Logic has built up core competencies in Cybersecurity, Training, Network & Internet Engineering, Project Management, Program Management and Logistics. Founded in 1992, Predicate Logic is a woman-owned, employee-owned, high technology engineering service company.
Predicate Logic's employees routinely receive many accolades and awards from its customers. The corporate headquarters is in the Sorrento Valley area of San Diego, California. Predicate Logic also has offices in Chesapeake, Virginia, specializing in communications engineering, network baselining, training, and Cybersecurity, and in Charleston,
South Carolina, supporting the Navy's SPAWAR System Center. SECURITY CLEARANCE: Applicant must hold an active Department of Defense (Do D) Secret personnel security clearance.
RESPONSIBILITIES: Apply quality processes or Quality Management System (QMS) processes that coincide with the Government's Manage Quality processes which address Quality Control, Quality Assurance, Software Quality, and/or project Quality System tasks. Perform quality control inspections necessary in the performance of the various tasks as assigned and identified in the Quality Assurance Plan or by the respective WBS, POA&M, or quality system/QMS documentation. Assure that the software products meet quality and
process standards as required by the contract. EXPERIENCE: Ten (10) years of experience in technical issue resolution.
Engineering and/or software design/maintenance training. Possess a practical understanding of engineering concepts. Ensure product, service and process meet quality and safety standards. Ability to interpret plans and drawings. Experience using computer aided drafting (CAD). Familiar with material specifications and fabrication methods. EDUCATION: High school diploma/GED, related military experience or trade/industrial school graduate. Predicate Logic's equal employment opportunity applies to all aspects of employment including, recruitment, hiring, training, promotion, transfer, compensation, benefits, educational opportunity, dismissal, social and recreational programs.
Job Posted by Applicant Pro
also provides cost-effective commercial training and digital forensics services. Predicate Logic has built up core competencies in Cybersecurity, Training, Network & Internet Engineering, Project Management, Program Management and Logistics. Founded in 1992, Predicate Logic is a woman-owned, employee-owned, high technology engineering service company.
Predicate Logic's employees routinely receive many accolades and awards from its customers. The corporate headquarters is in the Sorrento Valley area of San Diego, California. Predicate Logic also has offices in Chesapeake, Virginia, specializing in communications engineering, network baselining, training, and Cybersecurity, and in Charleston,
South Carolina, supporting the Navy's SPAWAR System Center. SECURITY CLEARANCE: Applicant must hold an active Department of Defense (Do D) Secret personnel security clearance.
RESPONSIBILITIES: Implement company and regulatory quality standards for product manufacturing. Knowledge of industry and governmental quality regulations. Audit and review quality data according to procedures. Document results according to company policies. Resolve any supplier, manufacturing and quality operations related issues. EXPERIENCE: Five (5) years of experience in technical issue resolution. Engineering and/or software design/maintenance training. Possess a practical understanding of engineering concepts.
Ensure product, service and process meet quality and safety standards.
Ability to interpret plans and drawings. Experience using computer aided drafting (CAD). Familiar with material specifications and fabrication methods. EDUCATION: High school diploma/GED, related military experience or trade/industrial school graduate. Predicate Logic's equal employment opportunity applies to all aspects of employment including, recruitment, hiring, training, promotion, transfer, compensation, benefits, educational opportunity, dismissal, social and recreational programs. Job Posted by Applicant Pro
receiving and verifying sanitation activities. Identification of quality concerns and finding corrective action remedies is a large function of the job requirements. Ideal candidates will have previous supervisory or leadership experience with the ability to be detail oriented and accurately identify problems and corrections as necessary.
This is NOT an entry level position for training. A minimum of three years of recent continuous employment is required. 12 Hour Shift position, working nights. Other examples of the QC work performed are: Various tests for incoming ingredients, including sieve, NIR, moisture, and mycotoxin, salmonella and other bacterial tests. Other duties as assigned
such as: Routinely check operator paperwork for accuracy and completeness, check label, bags and seals. Also perform additional duties and functions as assigned by Quality Control Manager/Diamond Management.
Must be able to lift 50 pounds of product routinely Must be able to climb ladders and can't not be afraid of heights. This position is NOT funded for relocation and is open for immediate hiring. At Diamond Pet Foods, we believe in family. At Diamond Pet Foods, we believe in family. We pay 100% of Medical Insurance premiums, company paid Life Insurance, AD & D, and Long Term Disability Insurance (after 30 days) for you, your eligible spouse, and your dependents. Dental, Vision, additional
voluntary life and AD & D insurance, plus Short Term Disability coverage are also available at group discounts.
Some of our other benefits include six paid Holidays, Paid Time Off days (vacation), and a 401K retirement plan (upon meeting employment requirements and plan provisions). Diamond Pet Foods provides for equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, interactionual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws.
Diamond Pet Food Processors of South Carolina complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. We'd be proud to have you join our family. Diamond Pet Food Processors of South Carolina 100 Wood Trail Drive Gaston, SC 29053 No phone calls please. Job Type: Full-time Salary: From $23.75 per hour Benefits: 401(k) 401(k) matching Dental insurance Employee discount Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: 12 hour shift Supplemental pay types: Bonus pay Work Location: One location
manufacturing and services, enabling the digital-rail-and-transit ecosystems. Wabtec is focused on performance that drives progress, creating transportation solutions that move and improve the world. Wabtec has approximately 27,000 employees in facilities throughout the world.
Visit the company's new website at: http: //. It's not just about your career. or your job title.it's about who you are and the impact you are going to make on the world. Do you want to go into uncharted waters.do things that haven't been done to make yours and someone else's life better? Wabtec has been doing that for decades and we will continue to do so! Through our people, leadership development, services, technology
and scale, Wabtec delivers better outcomes for global customers by speaking the language of industry. Summary: The mission of the Quality Engineer is to ensure that products manufactured in the shop are capable and will meet specified quality standards.
Understanding of manufacturing processes for analysis of non-conforming parts to identify root causes and address appropriate corrective actions. Keep communication with customers internal and external customers to track solution of non-conformities and implement effective corrective actions that will prevent recurrence in the future. Duties and Responsibilities: Drive culture of quality and process discipline. Analyze non-conformity issues
and provide a disposition of parts, follow up in the quality system until completion of disposition.
Lead containment activities to minimize customer impact. Perform root cause analysis and corrective action to prevent recurrence in production line. Lead activities to ensure execution to quality metrics within assigned area. Establish and execute quality plan for compliance with international quality standards (ISO-9001, AAR, IRIS, etc. ) Establish quality control plans to drive proactive quality improvements in area of responsibility. Work on project(s) to improve process control, reduce defects, scrap and rework in the shop. Monitor and report quality KPIs lead propose and lead action plans to improve product or process quality.
Minimum Qualifications Bachelor's degree from an accredited university, from Mechanical, Electrical, Industrial Engineering, or similar career. Experience in Quality Assurance or similar roles. Experience with corrective action activities (5-Why, 8D, Etc. ) Fluent English with oral and written communication skills. Able to work in a cross-functional matrix environment. Experience at least 4 years in related areas. Blue print reading Understanding of Gauging concepts and measurement techniques Competencies, Knowledge, Skills and Abilities: Experience or good knowledge of Manufacturing assembly processes.
Experience or good knowledge of Microsoft Office (Excel, Power Point, Word, etc). Knowledge of Lean Six Sigma or Quality tools. Green belt or black belt certification preferred. Certified Internal Auditor. Ability to coordinate several projects/tasks simultaneously. Effective problem identification and solution skills. Authority: [ Defined decision-making level. The Plant GM is the main authority at site level. To be able to give authority, any employee in the organization shall first receive it from their manager or upper level, up to the General Manager.
] Authority to update, approve, and release product quality documentation. Authority to disposition any material on the floor. All WPT employees have the authority to stop the process they are performing, should the process become unsafe or the outputs nonconforming. Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
) Employee is required to stand for up to 4 hours per day. Employee is regularly required to lift and/or move up to 25 pounds, and occasionally lift and/or move 50 pounds. Requires daily face-to-face interaction with employees on production line. Work Environment: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. ) Office and manufacturing environments. May involve exposure to cold and hot temperatures, humidity, dust, vapors, fumes, vibration, and other loud noises from the plant.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals, and loud noise. Relocation assistance lump sum available for qualified candidates. Wabtec Corporation is committed to taking on the world's toughest challenges. In order to fulfill that commitment we rely on a culture of leadership, diversity and inclusiveness. We aim to employ the world's brightest minds to help us create a limitless source of ideas and opportunities.
We believe in hiring talented people of varied backgrounds, experiences and styles.people like you! Wabtec Corporation is committed to equal employment opportunity regardless of race, color, ancestry, religion, interaction, national origin, interactionual orientation, age, citizenship, marital status, disability, gender identity or expression, or protected Veteran status. If you have a disability or special need that requires accommodation, please let us know. PDN-9ae7c187-a3d7-46f0-b33b-b4d750899648
skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary The Microbial Solutions site in Charleston, SC is seeking a Quality Control Analyst. This role will, ensure the quality and integrity of product by testing incoming materials, excipients and final product.
Perform environmental monitoring of LAL (Limulus Amebocyte Lysate) and Crude Lysate production areas to ensure appropriate conditions are maintained. Perform Crude Lysate recovery procedures during the Bleeding Season. The QC Analyst will be responsible for the following: Ensuring the quality and integrity of product by testing PTS cartridges,
Limulus Amebocyte Lysate (LAL), incoming materials, and excipients. Perform Crude Lysate recovery procedures during the Horseshoe Crab Bleeding Season (Summer Months).
Long-Term Stability monitoring of samples. Using technical writing to perform investigations and complete exception records. Attention to detail in all aspects of work is essential. Job Qualifications The following are the Minimum Requirements for the QC Analyst position: Bachelor's degree (B. A. /B. S. ). An equivalent combination of education and experience may be accepted as a satisfactory substitue for the specific education and experience listed above. Computer literacy must include word processing, spreadsheet and
Technical Writing. The following are Preferred Qualifications related to the QC Analyst position, but are not required to be considered for this position: One year of experience with GMP products.
Prior experience with laboratory operations and auditing. Compensation Data The pay range for this position is $20-22 per hour USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry.
We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety backssment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges.
Our client base includes global medical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.
We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to xyz X@. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
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