Job DetailsJob Location: Tamarac, FL 33321Salary Range: $90,000.00 - $110,000.00Job Shift: DayJob Summary: This position is responsible for authoring and executing process validation protocols related to drug manufacturing processes. The role also includes compliance engineering responsibilities to ensure
The Senior Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) activities across the site. This role is responsible for ensuring validation protocols, risk assessments, PPQ studies, and
TSMS – Senior Process Validation Engineer The Senior Process Validation Engineer - Technical Services and Manufacturing Sciences (TSMS) will be responsible for leading all facets of Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing practices (cGMP)
Job Description Agilent Technologies Advanced Therapeutics Division (previously Nucleic Acids Solutions Division) is looking for a Process Validation Engineer to join their Process Validation team working at their state-of-the-art, contract Active Pharmaceutical Ingredient manufacturing facility that specializes in oligonucleotide chemistries
Process & Validation Project Manager (a minimum of 5 years of experience required) Location: Philadelphia, PA Employment Type: Full-time, mostly onsite About Us Are you ready to take the next step in your career? LAPORTE, a consulting engineering
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science &
Process & Validation Project Manager Location: Philadelphia, PA Employment Type: Full-time, mostly onsite About Us Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a
Roche Digital Validation System Strategy Leader At Roche, we believe its critical to deliver medical solutions now even as we develop innovations for the future. We are passionate about transforming patients lives and we are fearless in
Senior Engineer Or Scientist Of Process Validation The Senior Engineer or Scientist of Process Validation ensures that manufacturing processes meet the validation and regulatory requirements to ensure the process is robust and reproducible under normal operating conditions. This role involves designing, executing,
Process Validation Engineer Valspeca global provider of system validation and lifecycle servicesprovides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspecs mission is to provide a wide spectrum of services that
Job Posting TitleTRC Process Manager Agency695 OKLAHOMA TAX COMMISSION Supervisory OrganizationDivision Directors Job Posting End Date Refer to the date listed at the top of this posting, if available. Continuous if date is blank. Note: Applications will
ROLE SUMMARY The QMS/V&C Lead is responsible for driving GWE R&D Compliance Program and Systems across Global sites. The incumbent will oversee, manage, and assure overall adherence to the Compliance Program for GWE R&D and drive
Do you want your voice heard and your actions to count? Discover your opportunity with Mitsubishi UFJ Financial Group (MUFG), one of the world’s leading financial groups. Across the globe, we’re 150,000 colleagues, striving to make
Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients lives accessible to as many people as possible. As a world leader in sterile single
Senior Scientist - Downstream Process Development, mRNA Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better
Company Description: Crown Equipment Corporation is a leading innovator in world-class forklift and material handling equipment and technology. As one of the world’s largest lift truck manufacturers, we are committed to providing the customer with the
OBJECTIVE OF THE OFFICE/DEPARTMENT This is a requisition for employment at the Pan American Health Organization (PAHO)/Regional Office of the World Health Organization (WHO) Contractual Agreement:Non-Staff - National PAHO Consultant Job Posting:July 3, 2026 Closing Date:July
Job Description SummaryLocation: Morrisville, North Carolina Join Novartis and play a pivotal role in shaping the future of pharmaceutical manufacturing at our growing Morrisville site. As the Validation Lead, you will drive the site’s validation strategy across process, cleaning,
Principal Process Automation Engineer - ART0002 Company: Worley Consulting Primary Location: USA-NM-Artesia Job: Consultants Schedule: Full-time Employment Type: Employee Management Level: Individual Contributor Job Posting: Jul 6, 2026 Unposting Date: Aug 6, 2026 Reporting Manager Title: Technical