Software Verification and Validation Engineer - Marlborough

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for their accelerated growth of 300% in the last 3 years with over 5500+ employees globally. · ...

+ Job summary + Sequel is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. The Senior Validation Engineer will support our growing portfolio of Enterprise systems. · + Qualifications + BS in Computer Science, Software E ...

Sequel Med Tech is seeking a Senior Validation Engineer to support our growing portfolio of Enterprise systems. · Develop, execute, and maintain validation deliverables. · ...

The Validation Engineer will lead verification and validation efforts on industrial automation projects. · Approve test cases using Azure DevOps. · Create verification and validation reports. · ...

The Software Verification and Validation (V&V) Engineer is responsible for ensuring that software products meet the required standards and specifications before release.This role involves planning designing executing and documenting testing activities to verify and validate softw ...

The Software Verification and Validation (V&V) Engineer is responsible for ensuring that software products meet the required standards and specifications before release. · Develop and implement software verification and validation plans, protocols, and procedures. · Design, write ...

The Software Verification and Validation (V&V) Engineer is responsible for ensuring that software products meet the required standards and specifications before release. · ...

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. ...

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 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. · ...

Position: Validation Engineer. · Must be experienced in computer system validation using GAMP 5 methodology. · ...

The Senior Validation Engineer will work as part of a larger validation team to ensure the biotech facility equipment, utilities, processes, instrumentation and computerized systems are qualified and maintained in a validated state in accordance with appropriate regulatory guidan ...

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 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 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 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.This position is a field-based ...

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 Instrument Validation Specialist will support a diverse variety of Quality Control and Manufacturing Instrumentation. · ...

Leads the validation efforts associated with the operation of all GMP manufacturing systems in a highly automated biologics manufacturing facility. · ...

This time focus on Validation engineers with Aseptic Process or APS experience local to Massachusetts. ...