Work Location: St. Louis, Missouri Shift: No Department: LS-SC-POKPGA Team 3 Group 2 Recruiter: Beverly Dellisola
This information is for internals only. Please do not share outside of the organization.
Your Role:
At MilliporeSigma in St. Louis, MO, the Process and Analytical Development Group Lead will lead a team of analytical and process development scientists to develop and optimize bio-conjugation processes suitable for technology transfer to GMP manufacturing in a CDMO environment.
Responsibilities:
Serve as a subject matter expert in process and analytical development, perform troubleshooting, provide efficient and innovative solutions and support transfer to GMP manufacturing
Effectively communicate with customers, document experimental results, communicate results to all stakeholders, author development documentation, contribute information for customer proposals
Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approaches as needed to solve problems and mitigate risk, ensure methods and processes are in place for efficient GMP start
Independently lead project teams, influence work in other team members, lead process improvement initiatives, scout for new technologies and emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities
Day-to-day management of direct reports including coaching/mentoring, career development and performance reviews
Who You Are:
Minimum Qualifications:
Bachelor's Degree in Chemistry, Engineering, Biochemistry or other Life Science discipline with 6+ years of lab experience
OR
Master's Degree in Chemistry, Engineering, Biochemistry or other Life Science discipline with 2+ years of lab experience
OR
PhD in Chemistry, Engineering, Biochemistry or other Life Science discipline with 1+ years of lab experience
2+ years of experience managing/supervising projects
Preferred Qualifications:
Scientist with a background in both analytical and process development of biomolecules
Knowledge of GMP and regulatory requirements
Experience working with or leading matrix teams
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.