Location: Middleton
Company: Thermo Fisher
while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science,
our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations! Discover Impactful Work: Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence.
Performs a variety of complex sample preparation and analysis procedures to quantitatively measure medical and biomedical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.
Enters data into databases and reports. Performs self-review for own data prior to QC submission.
A day in the Life: Performs a variety of complex sample preparation and analysis procedures to quantitatively measure medical and biomedical compounds in a variety of formulations and /or biological matrices for stability and analytical testing. Works with multiple functional groups to meet business needs. Plans and organizes work with periodic supervision. Sets up and maintains analytical instrumentation. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. Ensures QA findings are addressed appropriately.
Aids and training to other team members. Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems. Communicates project status to project leader. Performs work assignments accurately, and in a timely and safe manner. Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
Qualifications - External Keys to Success: Education Bachelor's degree or equivalent and relevant formal academic / vocational qualification Experience Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities Preferred experience: HPLC and/or CGE experience, GMP documentation.
Demonstrated knowledge of multiple applicable techniques such as: HPLC, CGE, ELISA, PCR, and compendia testing. Biomedical Testing, Karl Fischer, UV-Vis, FT-IR, TOC Preferred experience: HPLC/UPLC and CGE Proficient in Microsoft Excel and Word Proven track record to interpret data by performing trend analysis Proven track record in technical writing skills Ability to independently optimize analytical methods Proven problem solving and troubleshooting abilities Good written and oral communication skills Time management and project management skills Ability to work in a collaborative work environment with a team Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees.
We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds. Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.
#Start Your Story with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Science Jobs refer to a broad category of careers focused on the pursuit of scientific research, practical applications of scientific knowledge, and the advancement of technology. These roles are typically found in sectors such as healthcare, engineering, environmental science, and pharmaceuticals. Key characteristics of Science Jobs include a strong emphasis on problem-solving, analytical skills, and a solid foundation in scientific principles. Individuals in these positions often engage in data analysis, experimentation, and innovation to contribute to scientific understanding and development. The field is dynamic and constantly evolving, offering a diverse range of opportunities for specialization and advancement.
Science Jobs are career positions specifically within the wide domain of science, spanning across various disciplines including biology, chemistry, physics, and environmental science, among others. These jobs often feature a focus on research, development, innovation, and exploration. They can be found within academic institutions, private sector companies, research organizations, and government agencies. Characteristics of science jobs include a strong emphasis on analytical skills, problem-solving, critical thinking, and a commitment to continuous learning to keep pace with evolving scientific knowledge and technological advancements.
Science Jobs refers to a category of employment that specializes in the field of science, encompassing a diverse range of professions including researchers, laboratory technicians, science educators, and many others engaged in scientific disciplines. These jobs are characterized by their focus on inquiry, exploration, and the application of scientific methods to understand the natural world. They often require a strong educational background in science, critical thinking, problem-solving skills, and sometimes, experience with specialized equipment or software. In today's world, Science Jobs are crucial for innovation, technological advancement, and addressing complex challenges in healthcare, environment, and industry.
and analytical services to solve your most difficult development challenges in Biologics. The Upstream Process Development team is responsible for the development and implementation of upstream processing methodologies and analytical procedures that can be easily transferred to the c GMP Manufacturing Team.
This position will perform multiple complex projects in Upstream Process Development while maintaining project timelines. The position will serve as a technical lead for the development of robust, high performing upstream processes with emphasis on transferability to c GMP manufacturing. This individual's knowledge will result in working independently on assigned tasks/projects, developing
and overseeing project plans to improve processes, and acting as a technical backup to the Director. This position plans and conducts work requiring independent judgment in the evaluation, selection, and substantial adaptation/modification of standard techniques, procedures and criteria.
This is a fulltime role working Days; Monday - Friday Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The Role: Provides expertise in process development for numerous mammalian cell lines. Initiates, directs and executes scientific development for innovation and process improvements. Acts
as the technical lead for Client development projects, communicates project status and effectively provides technical explanation/rationalization.
Researches and develops existing and new technologies/process improvements. Critically analyzes complex data, interprets and integrates experimental results with project objectives. The Candidate: Education: Ph. D. in Biotechnology, or related field with at least 4 years of laboratory experience in an industrial setting. MS in Biotechnology or related field with at least 8 years of industry laboratory experience. B. S/B. A. in Biotechnology, or related field with at least 10 years of industry laboratory experience.
Experience: Extensive mammalian cell culture experience Operating, maintaining, and troubleshooting stirred vessel bioreactors or fermenters preferably in an industrial setting Strong knowledge of latest upstream process development strategies Knowledge of the optimization of mammalian cell production through media and feed improvements Experience in Tech transfers Good documentation practices (GDP) Experience writing standard operating procedures Experience mentoring junior staff regarding laboratory procedures Why you should join Catalent: Fast tracked career growth, with annual performance review and feedback process Competitive base salary with other compensation incentives including yearly incentive plan Medical, Dental, Vision, and 401K are all offered on day one of employment 19 days of Paid Time Off (152 hours PTO) + 8 paid holidays Onsite gym, Catalent corporate discount perks, paid volunteer time off program and other benefits too numerous to mention!
Defined career path and annual performance review and feedback process Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety.
The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to xyz X@.
This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U. S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent.
No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U. S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request.
Please forward such requests to xyz X@ for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.
