QC Supervisor

Responsible for the microbiology testing and release of drug substance and raw materials in support of contract commercial manufacturing in a cGMP/BL-2 laboratory as a member of the Quality Control Microbiology group. Duties include supervising 2nd shift laboratory staff, scheduling testing in accordance with disposition timelines, maintaining equipment, reviewing and performing assays, reviewing and revising cGMP documentation, monitoring trends, participating in lab audits and regulatory inspections. Works with 1st shift supervisor to coordinate all laboratory activities.Assays are performed in compliance with USP and other regulatory body requirements and Wyeth standard operating procedures. This candidate should have strong experience in microbiology assays and familiarly with the Environmental Monitoring program. This position requires a keen attention to detail, good organizational skills, strong team and people skills. Actively support all direct reports and aid in career development. Previous experience working in a cGMP environment is highly desirable.Requirements:
Candidate will have Bachelor's degree in Biology, Microbiology, or other related scientific discipline; at least 5 years experience in a QC Pharmaceutical/Biotech environment.
This is a second shift position, the schedule/hours are Monday - Friday 2-10:30pm or 3-11pm.
Wyeth offers competitive compensation and benefits programs including stock
options, child-care subsidies, flex-time, business casual attire,
educational assistance and professional development programs. Please
forward your resume with salary requirements and job reference code to the
address below.For more information, visit our website at