Validation Engineer - Arlington

We are currently hiring for a EMPQ Validation Engineer to support a global biologics manufacturer during a critical qualification phase. · The focus is execution, data generation, and documentation. · This opportunity is well suited for a validation or QC professional looking to ...

We are seeking an experienced Validation Engineer with strong EMPQ expertise to support a new facility startup. This role will focus on protocol development, execution, and documentation for facility and equipment qualification activities.Develop and execute EMPQ protocols includ ...

· ←Back to all jobs at VBB · Validation Engineer / Specialist (Maryland/DC) · Validation Engineer / Specialist · Are you hungry to learn, grow, and own your career in · pharmaceutical validation? We're looking for a Validation Engineer / · Specialist who wants hands-on experienc ...

Firmware Validation Engineer. Develop and maintain automated test scripts using Python and other scripting languages to ensure comprehensive test coverage. · Develop and execute comprehensive test plans, test cases, and test strategies for firmware validation, including UEFI vali ...

Lead EMPQ planning, execution and close-out for GMP manufacturing and cleanroom spaces. Author, review and approve EMPQ Validation Plans, Qualification Protocols and Summary Reports. · ...

We are hiring a Senior Validation Engineer to own and lead Environmental Monitoring Performance Qualification (EMPQ) activities for a biologics manufacturing site operating in a GMP-regulated cleanroom environment. · Lead EMPQ planning, execution, and close-out for GMP cleanrooms ...

Validation Engineer / Specialist · Are you hungry to learn, grow, and own your career in pharmaceutical validation? We're looking for a Validation Engineer / Specialist who wants hands-on experience, regional travel, and a clear path to leadership. · What You'll Do · Support IQ, ...

Firmware validation engineer for remote position in the washington area. · ...

We are thrilled to present an incredible opportunity to join our high performing organization. · Welcome to the forefront of innovation in cutting edge patient treatments We are constantly pushing the boundaries of what is possible and redefining the standards of excellence. · Ou ...

We are looking for CQV Consultants with strong experience in periodic reviews to support ongoing compliance activities at an operational facility. · Perform periodic reviews of qualified equipment and systems · Assess continued compliance with GMP and regulatory standards · ...

We are thrilled to present an incredible opportunity to join our high performing organization. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. · ...

Lead EMPQ planning execution and close-out for GMP manufacturing and cleanroom spaces Author review and approve EMPQ Validation Plans Qualification Protocols and Summary Reports Develop update environmental monitoring risk assessments and contamination control strategies Provide ...

We are currently hiring for a well-established biologics manufacturing organization entering a critical EMPQ phase.The site is operating in a highly regulated GMP environment and requires a senior validation professional to take full technical ownership of EMPQ from planning thro ...

Job DescriptionThe candidate needs to have current industry Cleaning Validation knowledge, including autoclaves for drug products. · 5+ years of Cleaning Validation experience in Biotech/Biologics/Pharma industries. · ...

We are hiring a Validation Engineer to support QC laboratory systems with a focus on EMPQ activities. · Perform EMPQ validation for QC and laboratory equipment · Develop and execute IQ/OQ/PQ protocols for lab systems · ...

We are seeking an experienced DeltaV Automation Validation Engineer with deep hands-on expertise in DeltaV systems. · 10+ years of experience in CQV processes and methodologies · Strong, hands-on expertise with DeltaV DCS · Proven ability to develop CQV documentation independen ...

We are seeking an experienced DeltaV Automation Validation Engineer with deep hands-on expertise in DeltaV systems. This role supports commissioning, qualification, and validation activities across instrumentation and control systems. · ...

We are thrilled to present an incredible opportunity to join our high performing organization. · As a leader within the life science industry,Why choose Project Farma?Welcome to the forefront of innovation in cutting edge patient treatments We are thrilled to present an incredibl ...

· Who is USP? · The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we beli ...

Who is USP? · The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe ...