Job Locations US-MA-Framingham

ID

2024-1490

Category

Quality

Position Type

Regular Full-Time

This Senior Associate PQA position is the primary QA resource during manufacturing production activities, providing real time quality oversight for Drug Substance, Drug Product, and all other production and QC testing activities. This position will be required to proactively support cGMP compliance and interact with all departments within the company.

This position is based in our Framingham location and typically has a 5-day on-site expectation.

Key responsibilities:

• Ensure quality and regulatory compliance during on-the-floor processing.
• Work alongside manufacturing teams to ensure current and best practices are implemented consistently maintaining compliance with cGMP standards and keeping the plant in compliance with corporate quality requirements.
• Perform Quality walkthroughs and inspections on the floor, to maintain inspection readiness environment.
• Review and approve deviations, CAPAs, and change controls
• Review and approve executed production batch records, logbooks, data, and Certificates of Analyses.
• Perform verification of data to assist with batch disposition process.
• Review and approve quality documents from Manufacturing, QC, Facilities & Engineering, Validation and PD, such as: SOPs, batch records, logs, training forms, protocols, plans, summary reports, risk assessments, work orders, etc.
• Conduct training on procedures, standard work, safety, and cGMP related topics
• Assist internal and external audits and regulatory inspections

Other responsibilities:

• Proactively support cGMP compliance in the business by reporting on KPI performance
• Assist with the implementation and continuous improvement of the Quality System
• Support Clinical QA activities as needed
• Assist with vendor qualification or evaluation/inspection.
• Lead and participate in continuous improvements
• Other duties, as assigned

Educational requirements:

• Bachelor's degree in science preferrred

Experience and skill requirement:

• 3-5 years of quality or mix of quality/manufacturing experience in biotech or pharmaceutical industry.
• High level of attention to detail and excellent time management.
• A very organized and methodical approach to tasks.
• Strong written and verbal communication skills to interact with other functions
• Strong collaboration skills

Location:

• This position is based in our Framinghamlocation and typically has a 5-day on-site expectation.

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.

Share on your newsfeed