AbbVie
Senior Scientist, Quality Control (Temporary Position)
AbbVie, Barceloneta, Barceloneta, us, 00617
Senior Scientist, Quality Control (Temporary Position)
Company: AbbVie
Location: Barceloneta, Puerto Rico
Employment Type: Full-time (Temporary contract 1 year)
Job Overview Perform laboratory testing within a GMP environment supporting raw materials, in-process, finished product, stability, and validation. Analyze data, interpret results and ensure conformance to product specifications. Train laboratory personnel.
Responsibilities
Maintain GMP compliance for laboratory records and procedures.
Implement procedural changes and laboratory technique improvements.
Perform analytical test methods with minimal error.
Interpret experimental data for product specifications conformance.
Troubleshoot analytical techniques and instrument issues independently.
Initiate exception documents and develop scientific protocols for exception causes.
Qualifications
Bachelor’s degree in Science (Microbiology, Biology, Chemistry or Bio-Chemistry) with 6 years experience; Master’s with 4 years; PhD with 2 years.
Strong analytical and logical thinking skills.
Technical writing proficiency.
Experience in test method validation, investigations and troubleshooting desired.
Compensation & Benefits
1‑year temporary contract with competitive base pay.
Paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k).
Short‑term and long‑term incentive programs.
Equal Employment Opportunity AbbVie is an equal opportunity employer and is committed to 100 % compliance with applicable laws. Veterans, persons with disabilities, persons under 18 are protected. For accommodation or equal employment opportunity information, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html.
#J-18808-Ljbffr
Location: Barceloneta, Puerto Rico
Employment Type: Full-time (Temporary contract 1 year)
Job Overview Perform laboratory testing within a GMP environment supporting raw materials, in-process, finished product, stability, and validation. Analyze data, interpret results and ensure conformance to product specifications. Train laboratory personnel.
Responsibilities
Maintain GMP compliance for laboratory records and procedures.
Implement procedural changes and laboratory technique improvements.
Perform analytical test methods with minimal error.
Interpret experimental data for product specifications conformance.
Troubleshoot analytical techniques and instrument issues independently.
Initiate exception documents and develop scientific protocols for exception causes.
Qualifications
Bachelor’s degree in Science (Microbiology, Biology, Chemistry or Bio-Chemistry) with 6 years experience; Master’s with 4 years; PhD with 2 years.
Strong analytical and logical thinking skills.
Technical writing proficiency.
Experience in test method validation, investigations and troubleshooting desired.
Compensation & Benefits
1‑year temporary contract with competitive base pay.
Paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k).
Short‑term and long‑term incentive programs.
Equal Employment Opportunity AbbVie is an equal opportunity employer and is committed to 100 % compliance with applicable laws. Veterans, persons with disabilities, persons under 18 are protected. For accommodation or equal employment opportunity information, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html.
#J-18808-Ljbffr