Supervisor, Quality Control (Chemistry) overseeing method transfer and quality processes at Cardinal Health.
Compensation
Anticipated salary range: $82,100.00-$117,200.00
Responsibilities
Coordinates and supervises the daily activities of Chemists or business support staff in the performance of technology transfer, method validation/verification and method optimization
Serves as the liaison between Cardinal Health Quality Control and Client Quality Control in the performance of technology transfer, method validation/verification/development/optimization
Is a quality lead for the QC Chemistry team
Identifies quality events and works with QA/QC management to ensure each event is handled in accordance with site procedures and regulatory requirements
Oversees chemists and contractors who operate analytical equipment, perform analytical tests, interpret results and documents findings in accordance with SOPs and regulatory requirements
Requirements
Bachelor’s degree in chemistry or related science field
We are looking for a Senior Staff Process Development Engineer to join our Austin, TX team to develop manufacturing processes for complex catheters, perform process validation, and mentor less experienced engineers.
Responsibilities
Work in a team environment to accomplish scientific approaches to complex Catheter development.
Develop manufacturing processes for products in the area of complex catheters.
Perform process analysis, improvements and process validation (IQ/OQ/PQ)
Create reports and/or other communications to effectively report engineering findings.
Works with cross-functional teams to become a pivotal member of Confluent engineering
Lead the Manufacturing Science & Technology organization at the Halle radiopharmaceutical production site, driving process robustness, validation, and technical excellence.
Compensation
Expected Annual Base Salary Range for role: € 97,900 to € 146,900
Responsibilities
Set strategic direction for Manufacturing Science & Technology
Serve as key partner for site and platform leadership
Strengthen knowledge management and technical standards
Ensure robust product stewardship and oversight
Drive manufacturing process robustness and continuous improvement
Requirements
Master’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or related scientific discipline
Ready to shape the technical future of a manufacturing site? As Site MS&T Head (m/f/d), you will lead the Manufacturing Science & Technology organization in Halle and play a key role in strengthening product and process performance across the site.
Compensation
Expected Annual Base Salary Range for role: € 97,900 to € 146,900
Responsibilities
Set the strategic direction and objectives for Manufacturing Science & Technology at the Halle radiopharmaceutical production site.
Serve as the key Manufacturing Science & Technology partner for site and platform leadership.
Strengthen knowledge management, technical standards and inspection readiness across the department and site functions.
Ensure robust product stewardship and end-to-end technical oversight throughout the commercial product lifecycle.
Drive manufacturing process robustness, capability and continuous improvement in collaboration with site and global teams.
Requirements
Master’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or a related scientific discipline
Lead and manage a global team of manufacturing science and technology professionals for cell therapy products, overseeing technical oversight, process validation, regulatory submissions, and cross-functional partnerships.
Compensation
The annual base salary for this position ranges from $216,996.00 - 325,494.00.
Responsibilities
Define and execute the Global MSAT function strategy
Build, mentor, and develop a high-performing Global MSAT team
Serve as a core member of the CMC lifecycle management team
Develop technical standards and templates for process validation and market approval workflow
Represent Global MSAT in technology transfer and process characterization teams
Requirements
B.S. in Chemical/Biochemical/Biomedical Engineering
M.S. in Chemical/Biochemical/Biomedical Engineering
Ph.D. in Chemical/Biochemical/Biomedical Engineering
Senior MSAT Process Engineer supporting the introduction of new cell culture processes to large-scale GMP production at a biotechnological production site in Geel.
Responsibilities
Coördineren van de technology transfer van USP-processen naar GMP-productie.
Ondersteunen van productieactiviteiten op schaal voor nieuwe launches.
Opstellen van procesdocumentatie, batch records en samplingplannen.
Uitvoeren van procesanalyses, trendanalyses en monitoring van kritische parameters.
Ondersteunen van procesvalidaties en Process Performance Qualification.
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