Job Title. CQV Engineer. Location. Glendale, CA (Onsite). Job Description. We are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and/or biotech facilities in Glendale, CA. The ideal candidate will have hands-on experience with autoclaves, HVAC/AHU systems, clean utilities, laboratory equipment, and temperature mapping, ensuring compliance with cGMP and regulatory requireme...
Title: CQV EngineerDuration : 12 Months Location: Los Angeles, CA A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer for a 12-month project, this is an onsite position and is 40 hours/week. The client needs someone with Facilities CQV experience including EMPQ (environmental monitoring performance qualification), Vessel IQ/OQ/PQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Al...
Position: CQV Engineer. Location: Petersburg, VA. Experience: 5 years. Duration:12 months contract. Job Overview. This role focuses on leading commissioning, qualification, and validation efforts across facilities, utilities, and equipment within pharmaceutical and biotech environments. You'll be at the center of project execution, supporting planning, development, documentation, and hands-on validation work while keeping everything aligned with ...
Technical Source is currently in search of a Validation Engineer for an engineering services firm that services the Pharmaceutical/Biotech industry. This will be a 12-month Contract-to-Hire position that is based in Kenosha, WI. The ideal candidate for this role will have the ability to validate utility systems in a pharmaceutical environment.Responsibilities of the Validation Engineer include:Author and Execute Validation Protocols for Utility S...
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America...
Job Details. Responsibilities. Generate, execute, review, finalize, and approve validation/qualification protocols and reports. Manage and update project validation plans for specific projects. ssist and deliver amendments to the qualification(s) to ensure qualification compliance within agreed upon timelines. Utilize computerized asset management system for managing validation/qualification schedules. Generate operational and maintenance SOPs, F...
Job Description. A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer for a 12-month project, this is an onsite position and is 40 hours/week. The client needs someone with Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skids, and Cleaning Validatio...
Job Details. Responsibilities. A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer for a 12-month project, this is an onsite position and is 40 hours/week. The client needs someone with Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skids and Clean...
About The Job CQV Engineer. Job Title. C&Q Engineer (Mid -Senior Level) Clean Utilities & Downstream Equipment. Location. Greater Raleigh Area, NC. Industry. Pharmaceutical Manufacturing. Employment Type. Full-Time or Contract. Position Summary. We are looking for a. mid- to senior-level Commissioning & Qualification (C&Q) Engineer. to support project execution at a pharmaceutical manufacturing facility in the. Greater Raleigh area. This position...
A large pharmaceutical company in Los Angeles is in immediate need of a. CQV Engineer for a 12-month project. this is an onsite position and is 40 hours/week. This project will start in March 2025. The client needs. someone with. Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skid...
About The Job CQV Engineer. Position: CQV Engineer. Company Overview. PharmEng Technology is a leading global provider of engineering and consulting services to the pharmaceutical and biotechnology industries. We specialize in providing innovative solutions to our clients to help them achieve their goals in drug development, manufacturing, and compliance. Job Summary. We are seeking a highly motivated and experienced CQV Engineer to join our team...
