Key skills
Communication
About this role
Role Overview
- Perform & review analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures & policies
- Transfer of technology & processes in accordance with relevant project plans & timelines
- Supports Deviations
- Follow all safety and environmental requirements in the performance of duties
- Other accountabilities, as assigned
Requirements
- Minimum of a Bachelor’s degree in chemistry or relevant field of study from an accredited university required or an equivalent combination of education and experience
- May consider an Associate’s degree in chemistry or relevant field of study from an accredited university with a minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory
- May consider a High School Diploma or GED with a minimum of five (5) years of experience in a clinical or industrial/pharmaceutical laboratory
- Minimum of one (1) year of experience in a clinical or industrial/pharmaceutical laboratory required
- Ability to author scientific & technical reports a plus
- Able to perform routine testing per SOP & GMP standards a plus
- Basic troubleshooting for laboratory equipment a plus
- Knowledgeable in GMP & laboratory techniques a plus
- Must demonstrate attention to detail required
- Strong communication skills (verbal & written) a plus
- Skills or knowledge in the following discipline: Chemistry Analysis of tablets including UPLC and Dissolution desired
Benefits
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards