Verification & Validation Engineer (V&V Engineer) - Plymouth

The Validation Engineer is responsible for performing the necessary activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations. · This includes the creation and execution of Qualification and Validation doc ...

We are seeking a Validation Engineer for our client in the pharma manufacturing industry. The role includes creating and executing IQ/OQ/PQ on production equipment as well as process validations. · ...

The Validation Engineer is responsible for performing the necessary activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations. · ...

+ Validation Engineer with experience in regulated manufacturing environments required for validation activities and manufacturing process development. Key Responsibilities: Write, execute and report on validation activities including IQ OQ PQ. ...

Dice is the leading career destination for tech experts at every stage of their careers. · We are seeking a Validation Engineer – Preferably from a Medical Device Background to join our team. · The successful candidate will have experience in manufacturing and/or process engineer ...

validation engineer in medical device · writing and execution of validation protocols and reports (le iq oq pq etc.) · developing and implementing manufacturing processes preparatiori of specifications operator instructions process studies production readiness investigations root ...

Supports testing and validation activities for medical devices ensuring compliance with regulatory quality standards. · Develop Test Protocols aligned with design verification plans. · ...

The Validation Engineer will support Project Knight, a large-scale foundry capacity expansion project within the Raynham MA manufacturing facility. · ...

Akkodis is seeking a validation engineer for a six-month contract position in Mansfield MA. · The validation engineer will generate execute and document validation activities with a primary focus on sterilization and microbiology for medical devices. · This role ensures complianc ...

Akkodis seeks a Validation Engineer for a 6-month contract position in Mansfield MA. The ideal candidate has experience in medical device manufacturing industry. · Generate validation plans and protocols (IQ/OQ/PQ), and final validation reports with focus on sterilization and mic ...

The purpose of the Validation Engineer is to complete assignments in support of Quality and Engineering for equipment qualification new product development process validation and test method validation. · ...

We are seeking a detail-oriented Validation Engineer with around 3 years of hands-on experience to support validation activities across equipment processes utilities cleaning and computerized systems in a GMP-regulated environment. · ...

InvaGen Pharmaceuticals is searching for an experienced Manufacturing Validation Engineer. The role involves creating and revising GMP documents, preparing qualification & validation documents of equipment and computer systems. · Develops appropriate disposition metrics · Creates ...

The Validation Engineer will support verification and validation activities for electromechanical medical device systems. · ...

We are seeking a Senior Validation Engineer (CQV) with 5+ years of hands-on commissioning, qualification, and validation experience to support bio-pharmaceutical manufacturing projects.This is a field-based, execution-focused role supporting GMP facilities utilities process equip ...

We are seeking a detail-oriented and experienced Validation Engineer to join our quality assurance team. · The successful candidate will be responsible for ensuring that manufacturing processes and systems meet regulatory standards and internal quality benchmarks. ...

We are seeking an experienced Validation Engineer to join our team in the pharmaceutical or biotech industry. · Associate's degree with 4-6 years of knowledge and experience in GMP documentation required · Minimum of 4 years of experience in documentation and 6 years of related e ...

We are looking for a highly motivated mid-level CQV engineer to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their pharmaceutical manufacturing facility. · ...

We are looking for a highly motivated mid-level CQV engineer (5+ Years of Experience) with good interpersonal skills to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their pharmaceutical manufacturing facility. · ...

InvaGen Pharmaceuticals is searching for experienced candidates for the position of Manufacturing Validation Engineer. · ...

We provide a full spectrum of services including facilities utilities process and automation engineering top-tier quality compliance and regulatory affairs consulting and innovative recruiting solutions. · collaborate with Engineering QA Automation and construction teams to ensur ...