Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,
Job Description This position supports the operations through the initial qualification to validation maintenance of equipment, systems, facilities, and utilities. Responsible and accountable for performing activities such as Cycle Development (CD), Design Qualification, Commissioning and Qualification, Performance Qualification
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Current job opportunities are posted here as they become available. Validation Lifecycle & Periodic Review Program Manager Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology,
Cis-International-LLC in Vega Baja, Puerto Rico, seeks a highly skilled Commissioning and Qualification (C&Q) professional on a full-time, on-site basis to support a pharmaceutical manufacturing operation. The role leads qualification activities for facilities, utilities, equipment and
Base pay range $45.00/hr - $50.00/hr Recruitment Consultant @ US Tech Solutions | Helping Fortune 500 clients with their Manpower needs:Right Talent ~ Right Time ~ Right Place! Duration: 12 months Job Description: Primarily responsible for
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading and
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading and
Who we are At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading and
Validation Engineer job at US Tech Solutions. Thousand Oaks, CA. Duration: 12 months contract Job Description Experience needed: Cold Storage Validation Experience, Analytical Equipment experience, Preferably Lab Ops/Equipment Background, Drafting Documents. Primarily responsible for ensuring adherence to computer
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading and
As the Sr. Specialist Quality Engineering (QE) you will be responsible for the oversight of the Quality Risk Management, CQV, CSV programs for the Cell Therapy operation of the Tarzana facility. This includes Quality Review and
Senior Software DQA Engineer - Medical Device #2324 (Project Management) ECIs mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades
Senior Software DQA Engineer - Medical Device #7809 (Project Management) About ECI ECIs mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives
VTI Life Sciences (VTI) is seeking forward-thinking and ambitious industrial automation engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry
VTI Life Sciences (VTI) is seeking forward‑thinking and ambitious industrial automation engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry
CSV Consultant ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT