Associate Director, Quality Assurance - Devens, MA, US

The Quality Assurance Product Disposition Specialist is responsible for supporting quality and disposition activities at the Devens MA Cell Therapy manufacturing facility in accordance with Client policies standards procedures and Global cGMP The role will aid in the routine and ...

+Job Summary+Quality Assurance Specialist will execute label control tasks and logbook management on-floor operations. · +Qualifications+Experience: 2-3+ years of MFG experience; Prior GMP gowning experience required. · +Responsibilities+Execution of label control tasks and logbo ...

This role involves ensuring quality assurance of products through execution of label control tasks, logbook management, floor operations and gowning in compliance with GMP standards. · Execution of label control tasks and logbook management. · Floor operations (70-80% of their sh ...

We are in search of a dedicated and experienced QA Supervisor to enhance our dynamic and collaborative environment. · The QA Supervisor plays a pivotal role within the Watson-Marlow Quality team, in ensuring the highest standard of quality.This position serves as the primary rele ...

The Client is seeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. · ...

We believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. · We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, · and a desire to ...

The Client is seeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. · ...

++Client is seeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA.+ · +The Contractor Field QA Specialist is responsible for quality activities for the LSCC in accordance with Client policies, standards, procedures and Global cGMP. ...

+ Avantor is looking for a Quality Assurance Specialist to ensure quality standards are met in a biopharma production environment. This role will be a full-time position based out of our Devens, MA office. The expected pre-tax pay for this position is $45,000 - $79,500. · Support ...

Perform facility and process quality audits in accordance with GMP guidelines · Support work order management activities · Assist with microbiology preparation, testing, and sample release. · ...

+Job summary · +Performs quality audit of the Facility · +Follow GMP/GLP Guidelines+SkillsFood chemistry · Quality assurance · +Benefits · +Medical, dental & vision · +Critical Illness, Accident, and Hospital ...

Performs quality audit of the Facility process including GMP Support work order management. · Assist with micro prep testing and release of samplesFollow GMP/GLP Guidelines · ...

Avantor is looking for a Quality Assurance Specialist to ensure quality standards are met in a biopharma production environment. · ...

The Associate Director of Quality Assurance will be responsible for managing the quality assurance group and directing day-to-day operations to ensure quality assurance for Devens and North Andover sites. · ...

+Job summary · Bioconjugation Quality Assurance Supervisor at Veranova ensures compliance with global quality standards and regulatory requirements. · +Qualifications:Minimum 9 years of quality assurance (QA) experience in a GMP manufacturing setting. · Proven leadership experien ...

This role involves managing quality assurance for Devens and North Andover sites by implementing cGMP compliant practices. · ...

We are seeking a Quality Senior Specialist to join our team. The successful candidate will create and maintain master data in SampleManager LIMS to support laboratory testing activities and ensure business timelines are met. · Create and maintain master data in SampleManager LIMS ...

Provide Quality assistance and oversight to operations for in-process intermediates and manufactured products. · Assure the quality of manufactured products complies with all applicable regulations and guidelines. · ...

The Manager Quality Assurance Disposition Support will support the overall Quality Disposition organization by owning and driving quality system records performing product and change impact assessments supporting systems and data requests needed maintaining QD monitoring tools an ...

This is challenging and meaningful work that transforms lives of patients and careers of those who do it. · ...