Product Validation Engineer 3 - Bedford

The Senior Computer Systems Validation Engineer will be responsible for ensuring GxP computerized systems, including both on premises and Cloud/Server based applications, are validated and controlled in compliance with industry standards and regulations. · Provide CSV and CSA-bas ...

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

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. · ...

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 ...

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 ...

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

+ 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. ...

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 ...

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

We are seeking a Validation Engineer – Manufacturing to support qualification, validation, and documentation activities within a cGMP-regulated pharmaceutical manufacturing environment. · This role is responsible for preparing, executing, and maintaining equipment, process, · cle ...

A Validation Engineer is required for a full-time position in Fall River, MA. · ...

The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. · Develops appropriate d ...

We are launching a new food manufacturing facility and are seeking an experienced Validation & Commissioning Engineer to join our team. · This individual will lead the commissioning, qualification, and validation (CQV) of process systems, utilities, · and facility infrastructure ...

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

We are launching a new food manufacturing facility and are seeking an experienced Validation & Commissioning Engineer to join our team. · Develop and manage the Validation Master Plan (VMP) for the facility. · Plan, draft, and execute IQ/OQ/PQ protocols for process equipment and ...

+We are launching a new food manufacturing facility and seeking an experienced Validation & Commissioning Engineer to join our team. · +Develop and manage the Validation Master Plan (VMP) for the facility. · Plan, draft, and execute IQ/OQ/PQ protocols for process equipment and cr ...

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

We are hiring a Validation Engineer to support validation and qualification activities at a pharmaceutical manufacturing facility in compliance with cGMP and global regulatory standards. · ...

A leading life sciences organization is seeking a CQV Engineer / Senior Validation Engineer to support commissioning qualification and validation activities for GMP manufacturing systems and equipment. · Develop and execute IQ OQ and PQ protocols for manufacturing systems and equ ...

We are seeking a mid-to-senior level Validation Engineer to support both Opex and Capex projects in a pharmaceutical manufacturing facility. · The role requires experience with automation commissioning and qualification of process equipment, · including operation within a plant a ...