QA Associate III
About The Position
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position performs a range of routine and semi-routine QA Raw Materials activities to ensure compliance with Quality Assurance and regulatory requirements. Responsibilities include supporting audits, training programs, and documentation review for GMP operations. The role promotes a compliant cGMP environment by following SOPs and provides quality support for investigations related to GMP manufacturing events. It also generates and reviews documentation for batch disposition and batch record assembly. The individual can work independently, within guidelines, and as part of a team. Additional duties include leading projects and training junior staff.
Requirements
- High School Diploma or equivalent.
- Bachelor’s degree strongly preferred in a Life Sciences discipline or equivalent.
- Minimum of three to five (3-5) years of relevant GMP experience in documentation, QA on the floor, manufacturing, or equivalent.
- Knowledge of cGMP regulations and good documentation practices preferred.
- Strong organizational and analytical skills.
- Must be familiar with Microsoft Office applications.
Responsibilities
- Assists in regular follow ups with end users to ensure timely completion of open investigations and investigation activities.
- Assist in ensuring the adequacy of investigations performed in relation to manufactured drug product and drug substance to support the batch release process.
- Provides quality support in the review and approval of quality reports including deviations, OOSs, complaints, OOTIs, SCARs, and corrective and preventive actions (CAPAs).
- Generates and compiles lot file review documentation for batch disposition.
- Updates lot status in ERP system.
- Responsible for equipment inductions, revisions and record maintenance within the electronic database.
- Performs Technical Quality review of validation protocols and reports.
- Performs logbook documentation audits for cGMP regulated logs and SOPs.
- Creates, revises and approves procedures.
- Performs the review of equipment and facility related Change Control documentation.
- Assists with internal, client and regulatory audits.
- Assists with the generation of department metrics.
- Assists with developing recommendations for continuous improvement projects.
- Assists in the review and approval of production batch records and associated data for product disposition.
- Assists in the review and approval of controlled documents including standard operating procedures, protocols, and reports.
- Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
- Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
- Fosters a safe and environmentally sustainable workplace by following all PCI EHS policies and procedures.
- Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture.
Benefits
- paid time off
- health insurance coverage (including dental and vision)
- flexible spending account
- 401(k)
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
