Sun Pharmaceutical Industries-posted 3 months ago
Full-time • Entry Level
Billerica, MA
5,001-10,000 employees
Chemical Manufacturing

Sun Pharma is the world's fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. The position involves performing GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology.

  • Record GMP data, monitors and evaluates QC systems and equipment
  • Implement improvements to procedures, and revises SOP's and GMP documentation as required
  • Interact with internal and external auditors including government agencies and contract manufacturing representatives
  • Perform sterility and endotoxin testing for release, stability, and validation for raw materials, in-process and final products
  • Maintain Sterility and Endotoxin testing areas in a state of cGMP compliance
  • Perform and review growth promotion testing data for qualification of microbial culture media
  • Perform microbial identification related to product and environmental testing
  • Perform sampling of raw materials as required for QC testing
  • Perform routine quality control testing as required and monitors or evaluates systems, equipment (i.e. water systems, environmental chambers, sample collection and testing instruments/equipment)
  • Maintain records in paper based or computer based systems
  • Author and execute method validation/suitability protocols related to product testing
  • Author summary reports for executed method validation/suitability protocols
  • Author deviation reports and microbiological assessment reports related to departmental activities and product testing
  • Review Microbiology testing data as required
  • Coordinate receipt of raw material, in-process and final product samples for testing
  • Maintain metrics for receipt and processing of samples for microbiology testing
  • Provide technical input on product testing issues and instrumentation/equipment
  • Serve as liaison to service, calibration and technical representatives
  • Conduct and document assay failure and complaint investigations
  • Perform other duties as assigned
  • 2-4 years related experience in a Pharmaceutical/drug (FDA Regulated) industry preferred
  • BS in Microbiology or related field or equivalent industry experience is required
  • Experience in pharmaceutical microbiology and microbiology testing not limited to endotoxin, method validation, sterility, bioburden, microbial identification, growth promotion and environmental monitoring testing; ability to perform standard and non-standard microbiology techniques to analyze product
  • Excellent verbal, written and interpersonal communication skills
  • Proficient at following specific instruction (i.e. written SOPs)
  • Working knowledge of cGMP/GLP
  • Good computer skills including word processing and working with spreadsheets
  • Medical, dental and vision coverage
  • Life insurance
  • Disability insurance
  • 401(k) savings plan
  • Flexible spending accounts
  • Employee assistance program
  • Paid time off benefits, including vacation time and sick time
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