• Product Launch & Lifecycle Engineer III

    Boehringer Ingelheim (Columbus, OH)
    …knowledge of experimental methodology and design of experiments to support pharmaceutical development/ process transfer/ validation . Ability to define root ... related scientific discipline plus a minimum of 5 years' experience in pharmaceutical process or packaging engineering, quality assurance, product development,… more
    Boehringer Ingelheim (03/04/25)
    - Save Job - Related Jobs - Block Source
  • Regional Sales Manager - Facility…

    Eurofins (Raleigh, NC)
    …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Position Summary Eurofins BPT ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €6.5 billion in...Sales Manager to join our team, focusing on facility validation and environmental monitoring solutions for the biopharmaceutical and… more
    Eurofins (05/08/25)
    - Save Job - Related Jobs - Block Source
  • Senior Scientist, Small Molecule Method…

    Eurofins (Lancaster, PA)
    …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Job Summary: Eurofins Small ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €5.3 billion in...seeking candidates with expertise in method development and/or method validation . + Applies GMP in all areas of responsibility,… more
    Eurofins (05/03/25)
    - Save Job - Related Jobs - Block Source
  • Associate Scientist, Method Development…

    Eurofins (Lancaster, PA)
    …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Job Summary: Are you ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €5.3 billion in...develop your career? Eurofins Small Molecule Method Development and Validation team is seeking an entry level scientist to… more
    Eurofins (05/01/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director, Computer Systems…

    Bristol Myers Squibb (Summit, NJ)
    pharmaceutical industry. + Minimum of 8 years' experience performing/supporting pharmaceutical computer systems validation on pharmaceutical equipment or ... with our Cell Therapy team. T he Associate Director, Computer Systems Validation (CSV), Equipment Commissioning & Qualification (ECQ) supports the activities and… more
    Bristol Myers Squibb (05/08/25)
    - Save Job - Related Jobs - Block Source
  • Process Validation Engineer II

    Danaher Corporation (Fargo, ND)
    …development and delivery of solutions that safeguard and improve human health. The Process Validation Engineer II is part of the Technical Operations Department ... discoveries worldwide. You will be a part of the Process Validation team and report to the...company + Knowledge of regulatory and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and… more
    Danaher Corporation (04/23/25)
    - Save Job - Related Jobs - Block Source
  • Validation Engineer

    System One (Piscataway, NJ)
    …installations, and process changes by ensuring proper qualification and validation for pharmaceutical and biopharmaceutical production. + Author ... or related field). + Minimum 4+ years of experience in facilities validation , commissioning, and qualification (CQV) in the pharmaceutical or biopharmaceutical… more
    System One (04/22/25)
    - Save Job - Related Jobs - Block Source
  • Validation Lead, Quality Assurance

    Astellas Pharma (Westborough, MA)
    …for commissioning and qualification of facilities/utilities, equipment, automated systems, and process validation . + Author, execute, review, and approve ... validation documentation for facilities/utilities, equipment, automated systems, and process validation and assist with resolving technical issues, evaluating… more
    Astellas Pharma (03/25/25)
    - Save Job - Related Jobs - Block Source
  • QA Specialist III, QA Validation

    Fujifilm (College Station, TX)
    …final qualification requirements of TOP's for GMP facilities. + Single Use and Process Validation a plus. + Excellent written and oral communication skills. ... with qualification/computer validation experience. + Experience with qualification/ validation of process equipment, clean utilities, automation, sterile… more
    Fujifilm (04/18/25)
    - Save Job - Related Jobs - Block Source
  • Lead Validation Engineer or Specialist,…

    United Therapeutics (Silver Spring, MD)
    … professional looking to apply your expertise in a dynamic biotech and pharmaceutical environment? As a Lead Validation Engineer, Equipment, you'll be a ... title will be as a Validation Specialist) + 8+ years of relevant validation experience in a pharmaceutical /cGMP environment + Proficient knowledge of US and… more
    United Therapeutics (05/01/25)
    - Save Job - Related Jobs - Block Source
  • Validation Area Specialist

    Novo Nordisk (Durham, NC)
    …Support - OFP. Essential Functions + Participate & provide feedback to international corporate validation process group + Must be ability to work & communicate ... sites + Perform & review system, equipment, utility, & process revalidation per corporate science & risk-based validation...experience required + Minimum of five (5) years of validation related discipline experience in pharmaceutical or… more
    Novo Nordisk (04/23/25)
    - Save Job - Related Jobs - Block Source
  • Engineer, Validation

    Novo Nordisk (Bloomington, IN)
    …Team Novo Nordisk and help us make what matters. The Position The Validation Department consists of four teams; Equipment/Facility, Process , Cleaning and ... protocols including installation / operational qualifications and requalification's on process equipment and utilities + Revise validation documents including… more
    Novo Nordisk (05/08/25)
    - Save Job - Related Jobs - Block Source
  • Validation Engineer II

    Charles River Laboratories (Memphis, TN)
    validation protocols for cell processing equipment, lab instruments, cleaning, process , shipping, test method and other validation activities as ... that you can feel passionate about. **Job Summary** Reporting to the Manager Validation , the Validation Engineer II supports the qualification/ validation more
    Charles River Laboratories (04/28/25)
    - Save Job - Related Jobs - Block Source
  • Senior Principal Validation Engineer

    Curia (Albuquerque, NM)
    …Engineering, or relevant field + Fifteen (15) years relevant experience in pharmaceutical validation (aseptic/sterile product facility) + Experience with ... + Review and approve qualification, validation , re-qualification, and re- validation documents for equipment and manufacturing process protocols and… more
    Curia (04/04/25)
    - Save Job - Related Jobs - Block Source
  • Senior Quality Validation Specialist

    Curia (Rensselaer, NY)
    …Review the Master Batch Records (MBRs) of commercial products and assess the need of process validation based on the proposed process changes + Conduct ... to support the overall project timeliness and on-going projects + Author/review/approve process and cleaning validation protocols and master plans, supervises … more
    Curia (04/10/25)
    - Save Job - Related Jobs - Block Source
  • Sr Process Controls & Validation

    Regeneron Pharmaceuticals (Rensselaer, NY)
    process development team. + Analyzing development studies, enrichment studies, process validation and characterization studies, chemical stability studies, ... Regeneron is looking for a Sr. Process Controls & Validation Scientist for...in-depth knowledge of liquid chromatography; experience in analytical chemistry, pharmaceutical sciences and protein characterization using a variety of… more
    Regeneron Pharmaceuticals (04/23/25)
    - Save Job - Related Jobs - Block Source
  • Senior Validation Engineer

    Abeona (Cleveland, OH)
    …Physics, etc.) + 8+ years of experience in an Equipment and/or Process Validation Engineering role within a pharmaceutical or medical device company + Must ... articulate, and possess good writing skills. + Experience qualifying process equipment and facilities in a pharmaceutical ...issues. + Ability to design, execute and analyze manufacturing process validation studies. + Ability to manage… more
    Abeona (03/14/25)
    - Save Job - Related Jobs - Block Source
  • Validation Engineer

    PACIV (IN)
    Validation Engineer will manage various commissioning, qualification, and/or validation facets within our client's Biotechnology and Pharmaceutical sites. ... Master's degree in Engineering or a Technical discipline required + 2+ years of validation experience in the Pharmaceutical Industry + Comfortable with a 24/7… more
    PACIV (04/05/25)
    - Save Job - Related Jobs - Block Source
  • Senior Director, QMS Process Owner…

    BeOne Medicines (San Mateo, CA)
    …operations. + Lead the design, implementation, maintenance, and continuous improvement of validation and manufacturing process elements in the QMS. + Define ... **General Description:** Senior Director, Business Process Owner (BPO) for GxP processes, with a...(BPO) for GxP processes, with a specific focus on ** Validation and select Manufacturing** processes within the **Quality Management… more
    BeOne Medicines (04/26/25)
    - Save Job - Related Jobs - Block Source
  • Senior Cleaning Validation Specialist

    Catalent Pharma Solutions (St. Petersburg, FL)
    …internal departments, while providing customer service and support to the manufacturing process . + Author validation documentation including, but not limited to, ... degree in Science or Engineering required. + 5+ years' experience in the pharmaceutical industry performing cleaning cycle development and validation required. +… more
    Catalent Pharma Solutions (03/20/25)
    - Save Job - Related Jobs - Block Source