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Quality Assurance Senior Associate NS
Posted: 12/03/2025
2025-12-03
2026-01-03
Employment Type:
Contract
Job Category: Quality
Job Number: 4803
Job Description
The Sr. Associate, Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for ongoing bulk drug substance manufacturing and new product introduction, including development, clinical, and commercial operations.
The Sr Associate, PQA position will facilitate real-time decision-making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong partnership and learning environment between Manufacturing and Quality staff providing coaching, guidance and direction for manufacturing events, deviations, quality systems and compliance.
Responsibilities:
The Sr Associate, PQA position will facilitate real-time decision-making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong partnership and learning environment between Manufacturing and Quality staff providing coaching, guidance and direction for manufacturing events, deviations, quality systems and compliance.
Responsibilities:
- Quality oversight of new product introduction activities covering facilities, utilities, equipment, systems and process with alignment into the Quality Systems. May include support on commissioning and qualification and validation activities in addition to new document support.
- Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
- Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls.
- Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA), change control records and validations.
- Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements.
- Oversee and provide guidance during on-the-floor analytical testing.
- Ensure that changes that could potentially impact product quality are assessed according to procedures.
- Ensure that deviations from established procedures are investigated and documented per procedures.
- Alert senior management of quality, compliance, supply and safety risks.
- Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation.
- Identification and implementation of continuous improvement opportunities within our processes and systems.
- Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on-site inspections.
- High school/GED + 4 years work experience or Associate + 2 years work experience or Bachelor + 6 months work experience or Masters Degree
- Knowledge of process and facility equipment, ability to interpret and apply Good Manufacturing Practices (GMP); quality assurance or manufacturing experience in the pharmaceutical or medical device industry; written and spoken fluency required.
- Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment?. Strong GMP and GDP Behaviors.
- Knowledge of electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems, experience with deviations.
- Demonstrated ability to work as a team player and independently. Strong communication skills and ability to complete assignments and meet timelines.
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