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:
Working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, this role will serve as an individual contributor in the Process and Analytical Development organization. The role will involve working in a lab setting on process development and optimization for external customers in the field of Antibody Drug Conjugates (ADC) or other Antibody Conjugates. The role will include problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations.
Responsibilities:
Serve as a subject matter expert in process and analytical development, perform troubleshooting / providing efficient and innovative solutions, and supporting transfer to GMP manufacturing
Utilize customer-facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposals
Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensure methods are in place for efficient GMP start
Independently lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities.
Who You Are:
Minimum Qualifications:
Bachelor's Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 6+ years of research experience
OR
Master's Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 2+ years of research experience
OR
PhD in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 1+ years of research experience
Preferred Qualifications:
Extensive hands-on process development experience in chromatography, ultrafiltration, and/or reaction kinetics
Working knowledge of Microsoft Office suite and digital documentation (modern data acquisition systems and electronic notebooks) as well as experience with advanced data analysis and/or statistical software systems
Knowledge of GMP and regulatory requirements as well process transfers
Experience working with or leading cross-functional matrix teams
Excellent time management, written and verbal communication skills
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.
