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Manager

10-15 years
Not Disclosed
10 Jan. 1, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Manager
Date: Jan 1, 2025
Location: Tandalja - R&D
Company: Sun Pharmaceutical Industries Ltd

Responsibilities:

  1. Oversee the lifecycle management of development products, focusing on knowledge management and lifecycle management as per ICH guidelines.
  2. Manage process changes in early-phase development.
  3. Review clone development and cell banking documentation, ensuring regulatory compliance in plans and reports.
  4. Review product development documents, such as process development reports, process descriptions, and process control strategy documents.
  5. Review analytical development documents, such as method development reports and method qualification/validation protocols, ensuring compliance with the latest quality and regulatory requirements.
  6. Develop, implement, and continually improve the Quality Management System (QMS) at R&D through SOPs, manuals, training, and audits while aligning with corporate QA and site QA.
  7. Verify laboratory data and its integrity, ensuring good documentation practices and data reporting per ALCOA++ standards.
  8. Compile and review process and analytical documents for regulatory filing and CMC review.
  9. Control documents, issue working copies, verify raw data, and archive soft and hard copy documents based on ALCOA+ principles.
  10. Maintain knowledge of regulatory requirements for biosimilars and biologics, especially for USFDA, EMEA, Japan, and India.
  11. Contribute to dossier writing for various countries such as USFDA, EMEA, and India.
  12. Ensure “dossier writing” and “audit readiness” at all times, responding to audit queries from regulatory agencies, clients, and business partners.

Education and Experience:

  • MSc in Life Sciences / M. Pharm (Quality)
  • 10 - 15 years of experience in quality assurance
  • Strong understanding of regulatory guidelines (RCGM, CDSCO, ICH, ISPE)
  • Exposure to product development, analytical development, CMC, regulatory filing, and RCGM and CDSCO requirements for recombinant products.
  • Experience with filing in regulated markets (EMA/FDA/PMDA/TGA/HC/ANVISA) is preferred.
  • Exposure to lifecycle management for global product development is an added advantage.
  • Experience facing international inspections/audits from regulatory agencies, clients, and business partners is preferred.
  • Excellent verbal and written communication skills in English.
  • Experience with dossier writing.