Quality Control Scientist I/II
Jubilant Pharma Limited
Summary
The QC Scientist I/II performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition.
Job description
Both Levels
- Analyze raw materials, in-process, stability and final container products according to established procedures, and as directed by the supervisor.
- Record and review data in accordance with GxP to meet regulatory requirements and provide information relevant to product disposition.
- Perform studies to assess product or procedural problems under the direction of the supervisor.
- Assist in other forms of troubleshooting/investigations as directed.
- Prepare reports and assist with document revisions as directed by the Supervisor.
- Maintain training compliance on all procedures.
- Adhere to all aspects of plant safety programs and in keeping with GMP's or other regulations.
- Maintain and operate laboratory equipment in accordance with procedure.
Additional Responsibilities For Level II
- Demonstrate proficiency in core analytical assays.
- Participate in direct internal and/or external client interactions.
- Perform special assignments as directed by the supervisor.
Working Environment
- Ability to lift 25 pounds unassisted.
- Repetitive activity.
- Prolonged sitting/standing.
Requirements
- Bachelor of Science in Chemistry, Biology, or related hard science OR BA degree in hard sciences with 2 years of solid lab experience (Level I)
- Bachelor of Science in Chemistry, Biology, or related hard science OR BA degree in hard sciences with 3 years of solid lab experience (Level II)
- Pharmaceutical experience desired
- Ability to lift 25 pounds unassisted
- Repetitive activity
- Prolonged sitting/standing
Benefits
- Medical, Dental & Vision
- FSA & HSA
- Life & AD&D Insurance
- Short-Term & Long-Term Disability
- Employee Assistance Program
Company overview
Jubilant Pharma Limited is a global integrated pharmaceutical company headquartered in Singapore with operations spanning multiple continents. As a wholly-owned subsidiary of Jubilant Pharmova Limited, the company operates through three core business segments: Specialty Pharmaceuticals, CDMO (Contract Development and Manufacturing Organization), and Generics & APIs. The Specialty Pharmaceuticals division focuses on radiopharmaceuticals with a network of 48 radiopharmacies in the US, along with allergy immunotherapy products where it holds a 25% market share in the US allergenic extract market. The CDMO segment provides contract manufacturing services for sterile injectables and non-sterile products, while the Generics & APIs business manufactures active pharmaceutical ingredients and solid dosage formulations. With approximately 5,200 employees worldwide, Jubilant Pharma operates six manufacturing facilities serving regulated markets including the US, Europe, and other regions across over 75 countries. The company is recognized as a 'Partner of Choice' by leading pharmaceutical companies globally and maintains strong market positions in radiopharmaceuticals, allergy therapy products, and several key generic formulations.