Quality Assurance Specialist
📋 Role Overview & Responsibilities
Are you an experienced Quality Assurance Specialist? Do you have experience working in the pharmaceutical manufacturing area? This might be a great job for you!
The main responsibility for this position is to provide quality oversight of manufacturing. Strong decision-making skills and independent thinking will be paramount for candidate success. The individual will work closely with Manufacturing, Quality, and Facility teams.
Key Responsibilities (must be familiar with, and can speak to, all below) Provide quality on-the-floor support of manufacturing, reviewing documentation, and providing real-time support of manufacturing issues change overs etc. Support quality decisions that may impact operations, ensuring appropriate escalation. Identify risks and communicate gaps for quality and GMP process/systems. Reviews and approves facility alarms, facility work order requests, and return-to-service documentation. Support, reviews and approves Deviations and CAPAs Authors and reviews SOPs, policies to ensure compliance and adherence to regulations/cGMP operations. Collaborate with Manufacturing to resolve equipment and process issues Support internal audits. Practice safe work habits and adhere to safety procedures and guidelines. Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements. Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions. Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections. Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.
MUST HAVE REQUIREMENTS: 4+ years of experience in the pharmaceutical/biotech industry Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards)
INTERESTED? APPLY NOW!FOR MORE IMMEDIATE CONSIDERATION, email a current resume to iris.levy@randstadusa.com TXT: YOUR NAME and QA to 954-308-6735
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This position is located in Burlington, MA with potential relocation and sponsorship assistance depending on candidate qualifications.
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