Sr Manager, QC Microbiology
About The Position
Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives. The Senior Manager, QC Microbiology will lead, develop, and direct the QC Microbiology and Sterility Assurance programs at the site. This role will develop and maintain all documentation with regards to testing requirements and strategies and serve as a subject matter expert (SME) for microbiology and sterility assurance issues and provide technical expertise aligned with current GMPs and current industry practice. Responsible for EMPQ and Quarterly and Annual EM/Utility Monitoring reports.
Requirements
- Bachelor’s degree in Microbiology, Biology, Chemistry or related scientific field.
- 8+ years relevant experience within the vaccine and biopharmaceutical industry with experience in aseptic processing required.
- 5+ years of supervisory experience or demonstrated leadership role.
- Demonstrated knowledge in Sterility Assurance program is required.
- Demonstrated knowledge of GMPs and FDA requirements is required.
- Must be able to critically evaluate data summaries and conclusions.
- Proficiency in MS Office products or comparable word-processing and spreadsheet skills are required.
- Must possess cGMP knowledge across all QC functions.
- Must have a knowledge and experience with cGMPs, 21CFR210, 211, 600, USP-NF, and Aseptic Processing Guidelines.
- Must be a team player.
- Ability to influence without authority and influence within a highly matrixed organization.
- Excellent interpersonal skills both verbal and written.
Nice To Haves
- Advanced degree (e.g. Masters) is preferred.
- Quality Systems experience desirable.
Responsibilities
- Lead, manage and professionally develop all staff members.
- Oversee the execution of EMPQ, Cleaning Disinfection studies, and ensure a compliant site EM/Utility monitoring program.
- Manage, develop and maintain the Environmental Monitoring Program and prepare quarterly and annual trend reports and provide suggestions for continuous improvement.
- Accountable for, but not limited to, testing of raw materials (microbial testing), utilities/environmental monitoring and in-process/final product samples.
- Assures that the QC laboratory operations are appropriately staffed and trained to meet both internal and external compliance (cGMP) requirements.
- Accountable for managing the sterility assurance program to ensure quality, product specifications and adherence to all current GMPs, ICH and FDA guidance documents, Annex 1, local procedures and Emergent Global standards.
- Ensure the laboratory remains current with all changes to applicable compendia and ability to implement changes in a timely manner.
- Review and approve technical protocols and reports.
- Review and approve out-of-specification (OOS) and out-of-trend (OOT) investigations and deviations.
- Manage relevant quality control activities and prioritize work to ensure site and project timelines are met.
- Interface with other departments and sites regarding special projects and quality issues.
- Coordinate and supervise collection of testing, trending, and data reported in the Quality Management Review and Annual Product Review.
- Liaise with Regulatory Affairs and prepare/review documentation required for regulatory submissions and change controls.
Benefits
- Eligibility for benefits is governed by the applicable plan documents and policies.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Manager
