Process Validation - San Diego

A biotechnology company in San Diego is looking for a Process Validation / Automation Engineer to develop and execute protocols for automated Cell & Gene Therapy Manufacturing Equipment. · Ability to Qualify / Validate Automated Manufacturing Processes for Cell & Gene Therapy pro ...

We are seeking a Process Validation / Automation Engineer / CGT / On-Site in San Diego · The ideal candidate has strong experience developing and executing Process Performance Qualification (PPQ) protocols for automated Cell & Gene Therapy Manufacturing Equipment. · Able to quali ...

Immediate hiring for Process Validation / Automation Engineer – (Contract-to-Hire) in San Diego. Develop and execute PPQ protocols for automated CGT manufacturing equipment and support CSV activities. · ...

Process validation engineer to develop and execute process performance qualification protocols for automated cell & gene therapy manufacturing equipment. · Qualify/validate automated manufacturing processes for cell & gene therapy products · Perform computer system validation and ...

We are seeking a Process Validation / Automation Engineer to support an upcoming Phase III trial. · Ability to Qualify / Validate Automated Manufacturing Processes for Cell & Gene Therapy products. · Experience preforming Computer System Validation and familiarity with Manufactur ...

Immediate hiring for Process Validation / Automation Engineer – (Contract-to-Hire) · ...

This is a Quality Engineer II role at a company in San Diego CA. · Responsibilities include validation experience quality reviews assessment of non-conformances change orders review and approve development studies attend project meetings draft validation protocols reports assist ...

We are seeking a Quality Engineer II to ensure compliance and quality throughout the manufacturing lifecycle of diagnostic and medical device products. · ...

A quality-driven professional with validation and process improvement skills is sought for this role at Hologic. · Proficient understanding of validation methods including process validation and analytical method validation. · ...

The Quality Engineer II is responsible for validation of analytical methods, cleaning, production process, equipment qualification, facilities/utilities qualification and raw materials qualification. · ...

The Quality Engineer II is responsible for validation of analytical methods, cleaning, production process, equipment qualification, facilities/utilities qualification, and raw materials qualification. · Gathers data to compile reports on quality compliance. · Liaises with cross-f ...

+The Quality Engineer II is responsible for validation of analytical methods, cleaning, production process, equipment qualification, facilities/utilities qualification, · and raw materials qualification. · Provides Quality leadership to new product development teams in the areas ...

The Quality Engineer II is responsible for validation of analytical methods, · cleaning, production process, equipment qualification, · facilities/utilities qualification, and raw materials qualification.Provides Quality leadership to new product development teams in the areas of ...

The candidate should have · 5 to 6 years of medical devices or diagnostic equipment manufacturing experience. · Manage the end-to-end validation documentation lifecycle including authoring, · reviewing and approving protocols (URS, IQ, OQ, PQ,PV,TMV,Rtm,VSR) Change Controls · & ...

Verification & validation Engineer will have the following responsibilities: A strong technical background and experience in the medical device industry (Translation of User/Business Needs to System Requirements, Requirements Management, System Architectural Development, Function ...

We are seeking a highly motivated and experienced Senior Engineer to lead multi-product project execution, · technology transfer,and manufacturing support efforts at our clients Southern California facility.The ideal candidate has a strong background in medical device · manufactu ...

This position supports day-to-day sustaining activities in a manufacturing environment and has direct interaction with Manufacturing and Process Engineering groups. · Provide ongoing quality engineering support throughout the product life cycle. · Ensure adequacy of non-conforman ...

This position is responsible for manufacturing and product Quality activities. · The position requires exceptional communication, interpersonal, and project management skills to effectively coordinate activities and deliver results. · ...

My client is a global leader in advanced engineering, prototyping and product development, · driving innovation across the medical device industry. · ...

We are seeking a Manufacturing Engineer II to support the introduction and industrialization of new life science manufacturing technologies within our Nitinol processing operations. · ...