valgenesis

CQV resources supporting an NPD large-cap project modifying existing equipment and processes for future methods in an existing large-scale cell culture facility. Focus on process equipment on the floor, walking systems down, and executing qualifications and related documentation. All validation documentation and execution in ValGenesis (e-validation...

Job-ID Reference Responsibilities: CQV resources supporting an NPD large-cap project modifying existing equipment and processes for future methods in an existing large-scale cell culture facility. Focus on process equipment on the floor, walking systems down, and executing qualifications and related documentation. All validation documentation and...

Job-ID Reference Job Description: Lead second shift CQV execution activities across multiple systems and workstreams. Coordinate daily execution priorities to recover schedule slippage and maintain timelines. Interface with QA, Engineering, and Operations to resolve issues in real time Oversee execution of IQ/OQ protocols and operational...

Job Description: Our client is seeking a Process Validation Engineer to support activities within a GMP pharmaceutical manufacturing environment. This individual will be responsible for developing, executing, and documenting process validation studies while partnering closely with Manufacturing, Quality, Engineering, Microbiology, and other cross-functional...

The Equipment Engineer (Equipment Commissioning & Qualification - ECQ) supports the successful implementation, commissioning, qualification, and maintenance of equipment, instruments, facilities, and utilities in a GMP-regulated pharmaceutical environment. The role is responsible for ensuring equipment remains in a commissioned, qualified, and validated...

Job Title: Project/Site Engineer — GxP Manufacturing Employment Type: W2/1099 Duration: 1 Year Job Summary: We’re seeking a Project/Site Engineer with GMP pharma/biotech experience to support manufacturing systems, CQV activities, change controls, deviations/CAPAs, and GMP documentation in a regulated environment. Experience with BMS, EMS, SCADA, and...

Job-ID Reference Summary : We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment. This is a fast-paced opportunity focused purely on execution of validation protocols—ideal for professionals who thrive on the manufacturing floor. Roles & Responsibilities: Execute IQ/OQ protocols...

We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate will be responsible for planning, executing, reviewing, and approving validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with...

Job Description Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines Interface with QA, Engineering, and Operations to resolve issues in real time Oversee execution of IQ/OQ protocols and operational verification activities Lead second...

Job Description Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines Interface with QA, Engineering, and Operations to resolve issues in real time Oversee execution of IQ/OQ protocols and operational verification activities Lead second...

Our client is seeking a Process Validation Engineer to support activities within a GMP pharmaceutical manufacturing environment. This individual will be responsible for developing, executing, and documenting process validation studies while partnering closely with Manufacturing, Quality, Engineering, Microbiology, and other cross-functional teams. The role...

Job-ID Reference Remote 50% Remote Job Description: Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines Interface with QA, Engineering, and Operations to resolve issues in real time Oversee execution of IQ/OQ protocols and...

Job DescriptionJob DescriptionSenior Industrial Engineer - Contract DISHER is seeking a Senior level Industrial Engineer to support a 2-year project with our customer team in the Medical Device industry.    What it's like to work here:Make a positive difference! It’s why we exist. We are always looking for teammates who are eager to use their diverse...

Pay Range: $50.00hr - $55.00hr Job Overview: Experience implementing or supporting C&Q, validation, quality, or other enterprise GxP applications, preferably in the pharmaceutical/biotech industry. Enterprise application implementation and production support experience. Experience working with SaaS applications and software vendors. Understanding of GxP and...

We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate will be responsible for planning, executing, reviewing, and approving validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with...

Job Description Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ protocols, equipment verification, temperature mapping, SIP/CIP validation activities, deviation support, and ensuring compliance with GMP/GDP...

Salesforce Business AnalystRemote Key Responsibilities• Requirements & Analysis: Partner with Product Owners, SMEs, and Business Stakeholders to elicit, document, and refine business and technical requirements, ensuring user stories have clear acceptance criteria within an Agile delivery framework. • Agile Delivery Support: Participate actively in sprint...

Work Your Magic with us! Start your next chapter and join MilliporeSigma.Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream...

Senior Industrial Engineer - ContractDISHER is seeking a Senior level Industrial Engineer to support a 2-year project with our customer team in the Medical Device industry.What it's like to work here:Make a positive difference! It’s why we exist. We are always looking for teammates who are eager to use their diverse set of talents with our customers,...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General DescriptionThe Director, Quality Systems will...