Director of validation jobs in United States

FPC of Greensboro has partnered with a growing pharmaceutical manufacturing client in their search for a Director of Validation. · This is a full-time role with excellent salary and benefits available. · We are seeking candidates with BS degree (MS/Ph.D. is a plus) and at least 5 ...

The Director of Validation will be responsible for all validation activities at the site, including facilities/utilities, processes, cleaning, equipment, CSV, and aseptic operations. · ...

We are seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. · Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements · Work in ...

We are seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Indianapolis, IN. · ...

About the job · Performance Validation is seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Kalamazoo MI. The Level I/II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams h ...

We are seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Kalamazoo MI. · Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements · Work in ...

This is a full-time on-site role for a Validation Professional located in Puerto Rico. · Proficiency in cGMP regulatory compliance and industry standards including FDA ISO GAMP 5 GLP GMP and 21 CFR Part 11 · Experience with validation including facilities utilities equipment comp ...

We are seeking a full-time Level I Validation Engineer/Specialist to join our teams in Indiana. This role will provide an opportunity for professional development, implementation of new services, and cultivation of new geographical areas. · The ideal candidate will have a strong ...

This is a full-time role for a Validation Engineer supporting Facilities, Utilities and Manufacturing system testing in the San Francisco Bay Area.Developing validation protocols and performing functional verification are key responsibilities. · ...

+We are inviting US CANDIDATES ONLY who wants to start their career in Life sciences/ Pharmaceuticals with recent graduate degree in any of these fields. We specialize in opportunities within Computer System Validation (CSV), Regulatory Affairs, Clinical Development & Drug Safety ...

This is a validation associate job description. · ...

Cleaning validation is required. · Expertise in Risk Based Approach for Commissioning and Qualification practices. · Planning and Integration of Commissioning and Qualification activities in medical device manufacturing (Class II preferred). · ...

This is a full-time role for a Validation Engineer located in the San Francisco Bay Area, CA supporting Facilities, Utilities and Manufacturing system testing. · Strong expertise in Validation and Good Manufacturing Practice (GMP) compliance. · Strong MS Word and Excel experience ...

We seek a highly technical leader for our Director opening in Ohio. · Bachelor's Degree required12+ years' experience in cGMP pharmaceutical manufacturing environment.Detailed working knowledge of GMPsClinical and commercial manufacturing support through facilities,equipment,clea ...

Want to learn more about this role and Jobot? Click our Jobot logo and follow · our LinkedIn page · Job details: · Remote Sr Program/Director, Computer System Validation within GXP & CXR lab settings. Strong workflow and documentation background at the Program Management levels. ...

We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Join us and be part of building the bridge between life changing therapies and patients. · Life changing therapies. Global impact. · Bridge to thousands of biopharma companies ...

The Director of Validation is responsible for leading validation activities at a sterile pharmaceutical manufacturing site. · ...

This leadership role is responsible for overseeing and advancing all validation activities across a commercial sterile manufacturing site. The Director of Validation ensures that facilities, utilities, equipment, processes, cleaning systems, and computerized systems remain in a v ...

Kelly Engineering is seeking a Director of Validation for a sterile pharmaceutical manufacturing facility in Sacramento, CA. · ...

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. · ...