valgenesis

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 execution...

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 for process...

Job-ID Reference Remote50% 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 operational...

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 verification...

Use Your Power for Purpose At Pfizer, the impact you will have on improving patients' lives is profound. You will play a crucial role in navigating and interpreting the growing regulatory demands to ensure optimal patient care. Your expertise and commitment are crucial in adapting to these changes and maintaining the highest standards of patient care. Join...

At least 10 years of experience supporting and/or performing all aspects of computer systems validation activities including development of scalable validation strategies, documents, and perform document reviewsAt least 7 years prior experience in computer systems validation within GMP/GxP regulated environmentsProven experience developing full validation...

### **Industrial Engineer - Contract** DISHER is seeking an intermediate 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...

Industrial Engineer - Contract DISHER is seeking an intermediate 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,...

Job-ID Reference 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...

Job Description: This role is responsible for system administration, validation, and operational support within a life sciences environment to ensure compliant, reliable, and efficient systems. Responsibilities include leading validation activities (authoring, execution, and review of protocols), project management and administering both GxP and...

Job-ID Reference Summary : We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized system validation within a GMP-regulated pharmaceutical environment. This role requires strong knowledge...

SAP CRM Functional Consultant 10+ years of hands-on experience in SAP CRM functional consulting, including implementation, enhancement, and production support projects. Strong expertise in SAP CRM Order Management, including order creation, service requests, returns, credit memo, and debit memo processes. Extensive experience in SAP CRM and SAP SD...

Job-ID Reference Job Summary: 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,...

This is what you will do: This Development Scientist II will be a key team member in Alexion’s External Analytical Development and Quality Control group. This position is responsible for maintaining the highest standard of quality and compliance of external quality control testing (GMP) laboratories. This candidate will be responsible for initiation and...

Job-ID Reference Job Summary: Senior CQV Engineer / 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...

DescriptionThis position provides leadership and accountability for Digital Quality across the organization’s Quality, Regulatory, and R&D systems landscape, with responsibility for supporting computer system validation activities in alignment with applicable regulatory expectations, internal procedures, and data integrity requirements. The role is focused...

Position Overview: We are seeking an AI Enabled Automation Architect dedicated to Site Automation Engineering to support advanced pharmaceutical manufacturing initiatives. This role focuses on the continued development, maturation, and application of reusable phase libraries, equipment module abstractions, and digital knowledge structures that enable...

Job-ID Reference Remote50% Remote Job Description: Senior CQV Engineer / 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,...

Job Title- Digital C&Q Application Engineer Job Location- Princeton, NJ (Hybrid, In a week minimum 3 days work from office) Job Description- Qualification & Experience: • Experience implementing or supporting C&Q, validation, quality, or other enterprise GxP applications, preferably in the pharmaceutical/biotech industry. • Enterprise...

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric...