validation engineer jobs in Fall River, United States

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 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 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 ...

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

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. · ...

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. · ...

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 ...

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

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

+ 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. ...

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 ...

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. · ...

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 ...

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

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

Kelly Services is seeking a Validation Engineer for a long-term engagement at a client in Jacksonville, FL. · Lead equipment validation lifecycle activities per procedure: User Requirements Specification (URS), Design Qualification (DQ) support, Installation Qualification (IQ), O ...

We're ramping up risk mitigation and CAPA remediation efforts · This is a hands on, cross functional role partnering with Product Design, · Facilities, Lab, and Microbiology teams.Drive design transfer for processes tied to endotoxin requirementsCreate · and execute Validation ...