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Associate Scientist II, Stability Coordination - Biologics - Kansas City Missouri
Company: Disability Solutions Location: Kansas City, Missouri
Posted On: 05/16/2024
Associate Scientist II, Stability Coordinator - Biologics --Position Summary:Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.----Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture.-- The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II, Stability Coordination - Biologics. Associate Scientist II under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians / assistants. Comply with divisional and site Environmental Health and Safety requirements.This is a full-time role position: Monday - Friday, days.Catalent is committed to a Patient First culture through excellence in quality and--compliance, and to the safety of every patient, consumer, and Catalent employee.--The Role - Labeling, organizing and tracking the flow of documents, including spreadsheets, reports, protocols etc;
- Authors documents, such as stability protocols, text reports, certificates of analysis, and operating procedures;
- Performs parallel review of documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance;
- Develop and execute stability work plans/schedules independently, using customer milestones and Division/site performance standards and metrics;
- Review technical documents for accuracy, thoroughness and regulatory compliance;
- Identifies opportunities for improvement projects;
- Perform activities under cGMP as appropriate;
- All other duties as assigned;The Candidate
- Bachelor's Degree in Life Sciences or Physical Science field with 0+ years' experience required;
- High Proficiency in Microsoft Office, Word, Excel, Outlook required;
- Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs;
- Ability to learn and retain technical information;
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
- Strategy is focused on personal time management and efficiency.
- Well organized with ability to multitask.
- Ability to work effectively under pressure to meet deadlines.
- --Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds;Why you should join Catalent:
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