production quality assurance specialist - Lincoln, NH - beBeeQualityInspections

A Quality Assurance Specialist will support Commercial QA Compliance. · Support Deviation Review and Trending, · CAPA Review and Trending,Extension request review and trending · ...

The Quality Assurance Professional will work in the Internal QA team of Human Genetic Therapies Quality Assurance Department. · Responsibilities include support of Commercial QA Compliance and Operations. · Deviation Review and Final QA Approval. · Trending, support of Quality Sy ...

Mayflower Communications Company is looking for a Quality Assurance Specialist to join their Production Team. · ...

+4 years of experience in cybersecurity or information assurance + 2+ years of experience with maintaining the security posture of a cloud environment + Experience with evaluating and recommending cloud services, tools and technologies to improve efficiency and enhance system cap ...

· DescriptionThe Quality Assurance Professional will work in the US External QA team responsible for Contract Manufacturing (CMO) and Contract Test Laboratories (CTL) oversight within the Biologics Operation Unit Quality Assurance Department This unit oversees contract manufactu ...

Support · Commercial QA Compliance: Deviation Review and Trending, CAPA Review and Trending. · ...

The Quality Assurance Specialist supports DeepHealth products and product development, collaborating cross-functionally to guide product development. · The Quality Assurance Specialist works within the team to support Quality processes such as QMS training and CAPA management.The ...

The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed. · BS in chemistry, pharmacy, biochemistry or related discipline · Minimum 7 years QA GMP experience in biot ...

The Quality Assurance Principal supports DeepHealth products and product development along with the Quality Management System throughout the organization. · Actively engage cross-functionally within the organization. · Act as the Quality lead for design changes to existing DeepHe ...

+The Quality Assurance Principal is responsible for supporting · +Actively engage cross-functionally within the organization, such as with the Engineering, Clinical and Marketing teams, to develop new products within the Product Lifecycle Management (PLM) and New Product Introdu ...

The Quality Assurance Principal is responsible for supporting DeepHealth products and product development.. · Actively engage cross-functionally within the organization to develop new products. · Ensure compliance with applicable standards and guidances. · ...

We are seeking a Quality Assurance Specialist to join our team The QA Specialist will assist in ongoing regulatory and compliance activities under the direct supervision of the Vice President of Regulatory Affairs. · ...

HealthDrive is seeking full-time Quality Assurance Specialist to join our team The QA Specialist will assist in ongoing regulatory and compliance activities under the direct supervision of the Vice President of Regulatory Affairs. · Coordinate coding and documentation reviews of ...

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. · ...

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster. · ...

Duties include review of event documentation such as Batch records, Exceptions and Regulatory filings with production record review and Product disposition for drug substance device assembly and finished goods. · Skills required are knowledge of relevant government regulations ag ...

The main function of a Quality Assurance Inspector is to ensure that products meet established quality standards and regulatory requirements. · A typical Quality Assurance Inspector performs batch record reviews, · and collaborates with production teams to maintain consistent pro ...

Pfizer is seeking a motivated Quality Assurance Specialist to join their team in Andover, MA. · Evaluate products materials processes to meet quality standards regulatory requirements. · Collaborate with production teams maintain consistent product quality. · ...

The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility. · This role ensures non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated, · and c ...

+Job summary · Perform Quality Assurance role in the Quality Assurance Site Support team with oversight of investigations (Manufacturing investigations), document approvals such as SOP approval, change control approval and laboratory investigation approval. · Title: Quality Assur ...

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 ...