Assoc Prin. Scientist, Analytical R&D (2nd Shift: Lead)

MSD•Rahway, NJ

13h•Onsite

About The Position

The Pharmaceutical Analytical Sciences group has an exciting opportunity for an Associate Principal Scientist 2nd Shift GMP Supervisor based in Rahway, NJ. Join us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. The Associate Principal Scientist will serve as the scientific and operational supervisor for a team of specialists and scientists in Rahway supporting various GMP analytical activities including cleaning verification, method validation, solvent release, and in-process testing for drug substance and drug product across the entirety of our non-sterile clinical portfolio during 2nd shift operations at the Rahway site. The role will also require hands-on analytical lab support to enable the pipeline. This particular role is fully onsite during 2nd shift operations (3pm – 114:30pm).

Requirements

BS or MS in chemistry or related science with at least 7 years of industry experience with pharmaceutical drug substance and/or product development.
Ph.D. in chemistry or related science with at least 3 years of industry experience with pharmaceutical drug substance and/or product development.
Excellent scientific communication skills.
Demonstrated creativity.
Effective interpersonal and collaborative skills.
Demonstrated ability to lead teams to deliver high-quality results against firm deadlines.
Ability to partner in a team environment with cross-functional interactions to drive results.
Analytical Method Development
Analytical Testing
Cross-Functional Teamwork
GMP Compliance
Manufacturing Operations
Operational Excellence
Science Communication
Team Leadership

Nice To Haves

Prior experience managing a GMP analytical lab that supports cleaning verification, IPC, and solvent release.
Prior experience with lab investigations/deviations and compliance audits is a plus.
Current Employees apply HERE
Current Contingent Workers apply HERE
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Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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Responsibilities

Serve as a scientific and operational supervisor for a team of specialists and scientists supporting cleaning verification, solvent release, and in-process testing for drug substance and drug product during 2nd shift operations
Support execution of Good Manufacturing Practices (GMP) analytical activities such method validation and release testing
Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA+ principles.
Ensure on time, right first-time analytical testing to enable clinical manufacture of drug substance and drug product
Provide technical and compliance oversight for lab investigations and deviations and to troubleshoot in the lab as necessary
Review and approval of GMP data, analytical reports, and SOPs
Ensure operational excellence and drive process improvements
Work collaboratively with internal stakeholders and partners such as Global Development Quality and Pharmaceutical Operations.
Support internal and external compliance audit activities.