QA Manager

Full‑time Regular | FULL TIME | Salem, VA, U.S. Salary Range: $75,000.00 To $100,000.00 Annually PharmaLogic is the fastest‑growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside. We offer you an exceptional opportunity to join our dynamic team as a Quality Assurance Manager! If you have a passion for nuclear medicine and want to make a significant contribution to patient care while working in a stimulating and dynamic environment, then this opportunity is for you. QA Manager (1am to 2am start times; some shifts are 9am to 5 pm) Role Summary As the site Quality Assurance Manager, you will play a vital role in the PharmaLogic quality program to assure compliance with cGMP and other standards for the manufacture of drugs for administration to patients. You will be responsible for completion of required quality assurance tasks of finished drug product as directed by cGMP SOPs and serve as site expert on PET quality assurance. The position involves a hands‑on role in all quality assurance duties for the site, including materials acceptance and quarantine, batch release & record review, drug quality control, sterility, environmental monitoring, equipment maintenance/qualification/calibration, investigations (IR, OOS, deviation, etc.) and corrective actions (CAPA), SOP writing, maintenance and review, inspection readiness, data quality and integrity, ANDA documentation and other routine QA functions. You will also be responsible for training documentation for staff on QA related activities. Job Responsibilities and Duties Ensure compliance with all regulatory commitments and company policies and SOPs including cGMP and radiation safety. Actively promote adherence to SOPs, as well as safety rules and awareness; report and take initiative to correct safety & environmental hazards. Provide immediate notification of quality related issues to site Manager, PET Operations Management and Q&R as necessary. Oversee production operations to assure that PET drugs meet requirements for identity, strength, quality and purity. Perform PET radiopharmaceutical Quality Control (QC) in cGMP environment. Perform aseptic processing related tasks. Oversee quality assurance oversight of routine production, packaging and shipping of radioisotopes. Examine and approve/reject components, closures, in‑process materials, packaging materials, labeling and finished dosage forms to assure that all meet specification; manage onsite inventory quarantine and control process according to SOPs to assure specifications are met. Assure approved vendors are used and maintain documents and records, including COA. Review batch, laboratory and production records to assure completeness, accuracy and conformance before batch release; authorize or reject batch according to SOPs or oversee batch release by other qualified team members. Perform batch trending analysis. Notify facility manager if any recall is necessary to assure that recalled materials are not administered to patients. Initiate change to SOPs, participate in authoring and review of SOPs, maintain documents under control in QMS. Assure SOPs match processes and procedures in PET manufacturing operation and report concerns to Management. Document and trend deviations, IRs, events and initiate investigation and assure documentation of corrective actions and retraining as applicable. Initiate and complete CAPA investigation as deemed necessary and report results and trends. Maintain facility compliance with environmental monitoring and aseptic control; review and trend environmental monitoring results and all testing records. Provide training to staff on QA activities and SOPs. Assure staff is qualified for assigned quality tasks with documentation of training and qualification. Maintain records for inspection. Perform annual retraining upkeep of training files. Assure aseptic processing of samples and products, as per SOP. Assure aseptic processing area is suitably cleaned, maintained, controlled to prevent mix‑ups or contamination; ensure personnel are qualified in aseptic technique and cleaning of the area and that approved cleaning agents and processes are used according to SOP. Assure environmental monitoring records are complete and readily available, including annual personnel media fill qualifications. Assure equipment is functional, within calibration, suitable for use, maintained and documented per SOP. Assure equipment is qualified and operated under specified conditions; maintain vendor IQ/OQ and site PQ documents. Assure master production, laboratory controls/analytical tests and other control records are consistent with actual work procedures and any discrepancies reported to PharmaLogic Quality and Regulatory. Maintain records to comply with FDA and SOP requirements. Maintain, monitor and report on the location QA program to management. Serve as site lead for FDA and other agency, vendor and internal quality audits, as directed. Maintain site audit readiness by thorough records, personnel and facility review. Maintain site copy of ANDA and all related filing documentation up to date, available and organized for review. Draft ANDA related documents for submission including annual reports and other updates as required. Conduct periodic and annual quality audits, training, SOP review and other activities as directed. Job Requirements │ Skills │ Education BS/BA degree in a relevant scientific discipline (chemistry, physics, nuclear pharmacy, nuclear medicine, engineering, etc.) and a minimum of 3‑5 years of quality experience in the pharmaceutical industry, or an equivalent combination of education and experience preferred. Pharmacy tech certification a plus; experience with aseptic technique a plus. Experience working with ionizing radiation and laboratory equipment desirable, including troubleshooting and repairs. Strong analytical, critical thinking and customer service skills. Experience working on a cross‑functional team in a fast‑paced environment. Strong knowledge of cGMP environment and regulations. Knowledge of CFR21 Part 212 preferred. Strong attention to detail and experience with managing multiple projects and priorities. PharmaLogic offers a competitive compensation package and superior benefits. Benefits 401(k) retirement benefit program Medical Dental care Disability insurance Employee assistance program Extended health care Life insurance On‑site parking Paid time off Vision care Work Hours 1 am to 9 am start times; some shifts are 9 am to 5 pm. 40 hours/week. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class. PharmaLogic is an Equal Opportunity Employer. #J-18808-Ljbffr