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Director Validation Jobs in Chelsea, MA (NOW HIRING)

Pwc

Data Validation Risk - Director

Boston, MA

$155K - $410K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Director & Summary The Opportunity As a Data Validation Risk Director, within our Risk & Regulatory practice, you will ...

CAI

Validation Engineer

Boston, MA · On-site

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 0 - 4 years ...

CAI

Validation Engineer

Boston, MA

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 0 - 4 years ...

CAI

Validation Engineer

Boston, MA · On-site

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 0 - 4 years ...

Aequor

Specialist QA - Validation, cGMP

Woburn, MA · On-site

... Direct: 732-339-3518 - Ext 2065 Qualifications Bachelor degree in a science or engineering discipline No less than 5 years of experience in the pharmaceutical environment and validation Additional ...

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Director Validation information

What does a director validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the typical daily responsibilities of a director validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What are the key skills and qualifications needed to thrive in the director validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

What cities near Chelsea, MA are hiring for Director Validation jobs?

Cities near Chelsea, MA with the most Director Validation job openings:

Director Validation jobs near you
Infographic showing various Director Validation job openings in Chelsea, MA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Assoc. Director, Oligonucleotide Process Validation

Wave Life Sciences

Lexington, MA • On-site

$170 - $230/hr

Other

Posted 14 days ago

Job description

Wave Life Sciences is looking for an Associate Director of Process Validation and Tech Transfers in Lexington, MA. This pivotal role involves leading process validation, ensuring compliance with cGMP standards, and collaborating with cross-functional teams for technology transfers. The ideal candidate will have extensive experience in oligonucleotide manufacturing and a solid educational background in biochemistry or related fields.

Responsibilities include authoring validation documents, overseeing PPQ activities, and acting as the technical expert during regulatory audits. The position offers a competitive salary and comprehensive benefits, making it a great opportunity to make significant contributions to RNA medicine development.

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