- Cognizant (Little Rock, AR)
- …or equivalent experience. . 12+ years of automation experience in the pharmaceutical industry, with a strong preference for API/bulk manufacturing environments. . ... Proven experience leading cross-functional automation teams on large-scale pharmaceutical projects or programs. . Demonstrated ownership of full project lifecycle… more
- Astrix Technology (Wilmington, OH)
- …- 14/08/2025 Apply for Job _Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a experienced QC Scientist to join their team!_ ... background (chemistry too is a plus) with a MS or PhD and pharmaceutical indsutry expereince! **QC Scientist I** **Background** + Lead Team in project Coordination… more
- Mallinckrodt Pharmaceuticals (Hazelwood, MO)
- …Global Technical Operations organization. Responsibilities include analytical method development, validation , and transfer to internal and external GMP laboratories; ... timely execution of project deliverables. Essential Functions + Lead the development, validation , and transfer of analytical methods using techniques such as HPLC,… more
- Contract Pharmacal Corp (Hauppauge, NY)
- …of USP and FDA requirements. + Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. + Generate method ... validation protocols. + Execute methods validation and...and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. + Conduct… more
- Lilly (Pleasant Prairie, WI)
- …and integrity principles in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. The ... and integrity principles in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. The… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …investigations. + Prepare, and execute risk assessments, manufacturing sciences studies and/or validation protocols and reports, such as Validation Master Plans, ... Process Validation Lifecycle (mixing validation , process/hold times, membrane/resin lifecycle) and Material qualification in support of capital projects, process… more
- Amgen (Thousand Oaks, CA)
- …excellence in aseptic processing, technology transfer, process characterization, process validation and continuous process verification. Periodic shift work or on ... and/or own high-quality process technology transfer and other technical documents. **Process Validation & Regulatory Support** + Development of validation plans… more
- Lilly (Indianapolis, IN)
- …Engineers are responsible for technical aspects of the design, delivery, and qualification/ validation of the device assembly equipment with a specific focus on the ... and/or Electrical portions of the device assembly equipment design, delivery, qualification/ validation , and Computer System Validation : + Automated Control… more
- Curia (Albuquerque, NM)
- …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... is responsible for supporting Quality Management Systems and Computer System Validation efforts. Additionally, the CSV Systems Engineer III will provide guidance… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- …Plant, and the Centers of Excellence for Microbiology, Elemental Impurities, and Validation , to support the Generics Business The Sr. Director, Quality is ... products and processes Centers of Excellence for Microbiology, Elemental Impurities, and Validation The Sr. Director is responsible for Centers of Excellence for… more