validation engineer jobs in Raynham, United States

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 ...

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

+ 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. ...

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

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 ...

2-4 years of experience in manufacturing and process engineering. Strong technical writing skills with appropriate awareness of the intended audience. · ...

Manufacturing process validation (IQ/OQ/PQ), medical device manufacturing and new product introduction (NPI). · Gauge R&R · Metrology · ...

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

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. · ...

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. · ...

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 ...

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. · ...

This role supports manufacturing and quality operations through execution of process equipment and test method validations. · Execute and support process and equipment validations including IQ OQ PQ FAT and SAT · ...

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 ...

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 ...

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 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 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. · ...