We have an exciting opportunity for a Scientist I in the Quality Control Analytical Technical Support team. The successful candidate will need a strong analytical and compliance experience with proven troubleshooting/investigational skills. This position will support Quality Control through involvement with complex analytical and/or manufacturing investigations, method troubleshooting, method validation/transfer, and authoring of CMC analytical sections in support of regulatory filings/responses.

Responsibilities:

Contribute to the QC analytical lifecycle management program

Responsible for the management/leadership of method transfers and validations to internal and external laboratories.

Authors transfer/validation protocols and reports

Collaborates with Analytical Development regarding the introduction of new analytical technologies and instrumentation

Troubleshoots and investigates trends in performance of analytical methods used for release/stability and in-process assays

Provides analytical technical expertise for manufacturing deviations and OOS/OOT investigations by working in concert with Manufacturing and Quality Assurance

Serves as a technical liaison between Quality Control and Analytical Development

Works in collaboration with Analytical Development to identify improvements in the analytics that improve overall efficiency in QC Operations

Works in collaboration with development and manufacturing colleagues to implement analytical controls, and support manufacturing and testing at CMOs

Delivers analytical source documentation for CMC sections of IND/BLA filings and addresses technical inquiries from regulatory agencies to support clinical trial and commercial marketing applications

Builds and maintains strong working relationships with colleagues in Research and Development, Regulatory CMC, Quality as well as alliance partner counterparts, as applicable

Skills:

Analytical Development, Vaccine Development, GMP, quality control, compliance, investigation and analysis, method validation, method transfer, regulatory filing, Large Molecule, analytical method, regulatory standard, glp, validation protocol, analytical methods, release, stability, in-process assays, technical liaison, deviations, investigations, drug development, ICH, CMC guidance documents

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.