About the Job:The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities, equipment, computerized systems, and manufacturing processes. This position plays a key role in supporting multiple client programs across clinical and commercial manufacturing within a fast-paced CDMO environment.
Responsibilities:- Execute commissioning, qualification, and validation (CQV) activities for facilities, utilities, process equipment, and manufacturing systems.
- Develop, review, and execute IQ, OQ, PQ protocols and validation reports.
- Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities.
- Support technology transfer and startup activities for new client manufacturing programs.
- Prepare validation documentation in accordance with cGMP, FDA, EU GMP, GAMP 5, and 21 CFR Part 11 requirements.
- Support deviation investigations, CAPAs, change controls, and risk assessments related to validation activities.
- Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external vendors.
- Participate in FAT, SAT, commissioning, equipment qualification, and facility expansion projects.
- Maintain validation documentation and ensure data integrity throughout the validation lifecycle.
- Support client audits, regulatory inspections, and internal quality audits.
- Identify opportunities for continuous improvement of validation processes and engineering systems.
- Support multiple client projects simultaneously while ensuring project timelines and quality requirements are achieved.
Qualifications:- BS/MS in life science or related field with 9 years of experience in drug/biologics industry in GMP production environment in roles of validation/engineering
- Working experience in CQV for biotechnology/pharmaceutical facility is required
- Familiar with CSV in accordance to GAMP 5 and CFR Part 11
- Familiarity with process, cleaning, assay validation a plus
- Experience in aseptic fill/finish equipment qualification and aseptic process simulation (APS) is preferred
- Experience in authoring of validation protocols for utility and equipment required
- Familiar with GMP operational principles and practice
- Ability to work across functional groups for team collaboration
Pay range is estimated between $90k - $120k based on skill set and experience.
#PB
#AH
Benefits:Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
