Sr. Quality Assurance Specialist - Lexington, MA

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 ...

+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 ...

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

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 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. · ...

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 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 ...

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 ...

This Delivery Assurance Specialist role involves working with customers to improve delivery performance by tracking part delivery status. Applicants must have solid manufacturing experience with focus on root cause analysis. · ...

Clinical Quality Assurance Specialists provide clinical quality leadership for medical device clinical trials in compliance with GCP and ISO 13485. · Provide clinical quality leadership for medical device clinical trials in compliance with GCP and ISO 13485 · Guide and support cl ...

We're working with Peraton on this exciting opportunity. · ...

We are seeking a Quality Assurance Specialist to join our Human Services team. The ideal candidate will have experience in quality assurance and compliance with applicable regulatory requirements. · ...

In this role, you will be a part of the PTC revenue team reporting to the Revenue Assurance Senior Manager. · Perform contract reviews for revenue related contracts to determine appropriate accounting treatment under ASC606 and document conclusions · Review, recalculate, and anal ...

This position is responsible for conducting day-to-day activities including batch record review media disposition label issuance archiving and final product packaging and release activities. · The individual must be able to gown into classified manufacturing ISO 7 clean room area ...

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 ...

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 ...

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. · ...