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Supv Production

4-7 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote 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: Supervisor Production
Date: February 7, 2025
Location: Goa, India, 403722
Company: Teva Pharmaceuticals
Job Id: 60661


About Us:

At Teva Pharmaceuticals, we’re on a mission to make good health more affordable and accessible to help millions around the world live healthier lives. Our company is the world’s leading manufacturer of generic medicines and the proud producer of many products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people take one of our medicines every day. We’re always looking for new ways to make a difference and new people to help us achieve that.


How You’ll Spend Your Day:

  • Compression & Coating Area Management:

    • Oversee and ensure the upkeep of the Compression and Coating areas in Production.
    • Supervise daily operations of the Compression area within Production.
  • Documentation & SOPs:

    • Prepare and review Standard Operating Procedures (SOPs) and other documentation for manufacturing areas.
  • SAP System Management:

    • Handle SAP R/3 system for manufacturing-related transactions.
  • Investigation & Quality Management Systems:

    • Prepare and review investigations related to deviations, OOS (Out of Specification), OOT (Out of Trend), market complaints, exception reports, etc.
    • Initiate, review, and perform impact assessments of quality management systems such as change controls, CAPAs, and risk assessments as part of investigations.
  • Equipment & Compliance:

    • Sign off on equipment qualification documents as a business owner.
    • Ensure compliance, calibration, and preventive maintenance of all machines in manufacturing areas.
  • EDMS & Documentation:

    • Perform Glorya EDMS-related activities and ensure accurate documentation of all activities in areas worked.
  • Batch Manufacturing & Execution:

    • Perform batch manufacturing activities according to Batch Manufacturing Record (BMR) instructions.
    • Review executed batch manufacturing records.
  • Production Planning & Coordination:

    • Plan and execute daily production schedules.
    • Coordinate with cross-functional departments to ensure smooth production operations.
    • Manage material storage areas.

Your Experience and Qualifications:

  • Experience:

    • Minimum 4 to 7 years of experience in the compression and coating areas, specifically in OSD (Oral Solid Dosage) tablets production.
    • Experience in team handling is required.
  • Educational Qualifications:

    • Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) is mandatory.

How to Apply:

If you meet the qualifications and experience outlined above, Teva Pharmaceuticals invites you to apply for this exciting opportunity.