Total Base Pay Range: 47,100.00 - 67,300.00 - 87,500.00 EUR
Naast het basissalaris kun je, afhankelijk van vooraf bepaalde prestatiecriteria, in aanmerking komen voor een prestatiegerichte bonus.
Responsibilities
Afhandeling van OOx/deviaties, definiëren van CAPA’s en opvolgen van KPI-trends
Ervoor zorgen dat alle activiteiten voldoen aan cGxP, inclusief data-integriteitscontrole en goedkeuring van analytische data/tests (analytische vrijgave) en stabiliteit
Stabiliteitstesten binnen projecten: opstellen van protocollen, evaluaties en rapporten
Rapportage, waaronder het opstellen van stabiliteitsplannen, trendanalyses en evaluaties
Uitvoeren van stabiliteitsstudies, protocollen en vergelijkende rapporten voor leverancierskwalificatie
Requirements
Bachelor's degree in Pharmaceutical Laboratory Technology, Microbiology, Biotechnology, Chemistry or another relevant scientific discipline
Cytotechnologist responsible for preparing, staining, mounting, and microscopically examining cellular specimens to detect cancer and other abnormalities.
Responsibilities
Prepares, stains, mounts, and studies cells of the human body to detect evidence of cancer, abnormalities, and other pathological conditions
Prepares and examines microscopic slides from specimens of blood, scrapings, or other bodily exudates
Fixes and stains the slides to preserve specimen and enhance visibility of cells under the microscope
Works closely with the pathologist to report abnormalities
Works to produce lab tests in an efficient organized manner
Senior Scientist in Inhalations performing complex laboratory testing, method development, validation, and mentorship within a GMP analytical laboratory.
Responsibilities
Independently performs complex laboratory testing
Communicates analytical needs and resources
Maintains strong hands‑on laboratory presence
Assists with testing execution, troubleshooting, and optimization
Applies advanced scientific judgment
Requirements
Bachelor's degree in chemistry, analytical chemistry, pharmaceutical science or related field
The role involves independently performing complex laboratory testing and providing hands-on technical coaching and mentorship within the laboratory, specifically focusing on Mass Spec/Extractable and Leachables.
Responsibilities
Independently performs complex laboratory testing, including challenging routine testing, analytical investigation support, development, transfer, or validation activities.
Communicates analytical needs, resources, and/or barriers with relevant stakeholders.
Maintains a strong hands-on laboratory presence and serves as a technical resource during test execution.
Actively assists with testing execution, troubleshooting, and optimization rather than directing work from outside the lab.
Applies advanced scientific judgment to execution strategy, data interpretation, and problem resolution.
Requirements
Bachelor's degree in a relevant area, ie. chemistry, biochemistry
Support all Regulatory CMC aspects of an assigned product portfolio aligned with Zoetis business objectives, including veterinary drug development projects, regulatory change management, and routine registration maintenance.
Responsibilities
Develop global Regulatory CMC strategies for pharmaceutical dosage forms
Support CMC activities for new product development teams, including post-approval manufacturing changes and site transfers
Prepare responses to global health authority questions and information requests
Maintain awareness of emerging global biopharma/pharmaceutical CMC regulations
Build strong working relationships with Zoetis manufacturing sites and contract manufacturing partners
Requirements
Bachelor’s degree required
Nice to have: EU animal health regulatory processes
Comprehensive benefit packages including medical, dental, vision, mental health, paid time off, 403B, education assistance, voluntary benefits such as pet insurance, accident insurance, hospital indemnity
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