Quality Assurance Specialist - Lowell

+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 ...

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 ...

We are seeking a Quality Assurance Specialist for one of our largest pharmaceutical manufacturing companies in the Andover area. · Demonstrate sufficient depth of knowledge within own work area in order to perform hands-on routine QA tasks. · ...

The QA Investigation Reviewer ensures non-conformances/deviations are thoroughly investigated and compliant with cGMP regulations. · ...

This person will demonstrate sufficient depth of knowledge within own work area in order to perform hands-on routine QA tasks. This role supports Operations including batch record review, document review, and disposition activities. · ...

The Specialist Quality Assurance is responsible for providing support to the Quality Assurance department. · This role will work with cross-functional teams to maintain internal Quality Systems.Assist in the execution of Quality Systems to support GLP, GMP and GCP. · Review and h ...

The Specialist Quality Assurance is responsible for providing support to the Quality Assurance department. · This role will work with cross-functional teams to maintain internal Quality Systems. ...

Job Purpose · The Specialist Quality Assurance is responsible for providing support to the Quality Assurance department. · This role will work with cross-functional teams to maintain internal Quality Systems. · Key Roles and Responsibilities · Assist in the execution of Quality S ...

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 Specialist Quality Assurance is responsible for providing support to the Quality Assurance department. This role will work with cross-functional teams to maintain internal Quality Systems. · B.A/B.S in Life SciencesMinimum of 2 years GxP experienceStrong knowledge of MS Word ...

We are working on two medical devices that are going into expanded clinical trials and need someone with a strong quality background that understands medical devices. · These are a class 2 and class 3 medical device. · ...

6+ month on-site assignment in Boston, MA. · W2 employees or single member LLC professionals only · No C2C/third-party vendors · OVERVIEW · Our pharmaceutical client is in need of a Quality Assurance (QA) Specialist to support their team. · This consultant will work with the QA ...

The Quality Systems Specialist role involves contributing to planning and implementing the Pillar Quality Management System. Responsibilities include quality processes, procedures, work instructions, document control, change order processes, product development introduction proce ...

The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed. The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Tria ...

This is an individual contributor position with responsibilities for elements of the site quality system. · ...

+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. · ...

Intellectt Inc is hiring for QA professional for Medical Device company. · 5+ Years in Quality and Medical Device (13485, ISO, GCP) · ...

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 ...

++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. ...