Sr Scientist

• Coordinates and executes method transfers/method verifications/co-validations of testing procedures utilized within the Quality Control laboratory.
• Coordinates and executes the verification protocols to verify the vendor and USP analytical methods.
• Reviews the obtained results and verification reports after the execution of method transfers and verification protocols.
• Acts as liaison between I&D departments or Production Units and the QC Chemistry laboratory for the transfer and implementation of new testing procedures.
• Subject matter expert for performance of critical tests in support of new product launches.
• Knowledge leader within QC on the conformance of the release and stability profile as documented in the I&D development reports and regulatory submission.
• Identifies and investigates complex problems occurring in the QC laboratories and provides technical support in solving the problems.
• Prepares documentation for Regulatory Submission, as required.
• Reviews/updates/approves documentation such as protocols, test methods, SOPs, raw material/finished product specification, etc.
• Participates in the orientation and training of lab employees in new analytical method techniques.
• Capable of handling complex projects with only general guidance.
• Establishes work priorities for assignments within his/her authority and keep assignment completion on schedule.
• Functions as the analytical project leader in inter-departmental meetings.
• Provides project leadership to assigned scientists (i.e., grade 15 and below) and monitors performance of these individuals. Provides input to laboratory management of their performance to support the performance review, recognition, and disciplinary processes.
• Interfaces with Plant Operations and Technical Transfer personnel to support and resolve plant technical issues where analytical expertise is needed.

Requirements

• Possess a B.S. in Chemistry or Biology, or equivalent physical science. Typically, 8-10 years of experience in the pharmaceutical industry, or M.S. degree with 5+ years' experience, or Ph.D. with 3+ years' experience in analytical chemistry.
• Extensive knowledge of analytical chemistry as well as concepts in developing and validating methods to correct pharmaceutical standards.
• Extensive knowledge of parenteral formulations.
• Strong knowledge of GMP's, GLP, ICH, and USP guidance and regulations.
• Preparation of documentation for Regulatory Submissions as required.
• Able to review/approve/update documentation such as protocols, test methods, SOPs, specifications, ANDA submissions, etc.
• Strong analytical and problem-solving skills.
• Strong interpersonal skills and highly effective in team settings.
• Strong project management skills, written, and oral communication skills.

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is atwill, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.