Cipla ltd – Quality control Job openings for MSc / B Pharm Candidates – 44168

Cipla ltd - Quality control Job openings for MSc / B Pharm Candidates - 44168

    Career Opportunities at Cipla – Team Member QC (Requisition ID: 78972)

    Job Details:

    • Requisition ID: 78972
    • Location: Goa, India

    Job Description: Cipla, a leading pharmaceutical company, is offering career opportunities for the position of Team Member QC. This role is a part of the Quality division and involves preparing, updating, and reviewing specifications, Standard Operating Procedures (SOPs), policies, and operating documents related to the analysis of materials. The primary goal is to ensure alignment with predefined quality parameters and compliance with relevant standards, pharmacopeia, and cGMP (current Good Manufacturing Practices) requirements.

    Key Responsibilities and Accountabilities:

    I. Prepare and Review Documents:

    • Prepare documents such as SOPs, specifications, and non-routine documentation.
    • Coordinate with the site Quality Control/Quality Assurance teams to revise corporate documents.
    • Review applicable pharmacopeia and guidelines and make necessary updates.
    • Review instrument calibration data concerning operating documents.

    II. Stay Current with Pharmacopeial Updates:

    • Review the latest pharmacopeial updates, supplements, and amendments.
    • Evaluate updates required in existing documents to ensure compliance with current pharmacopoeia standards.
    • Collaborate with regulatory bodies to maintain compliance.
    • Timely communication to initiate and complete activities.
    • Escalate non-conformances to prevent operational delays.

    III. Ensure Document Compliance:

    • Review assigned documents by referring to relevant backup and quality procedures.
    • Follow approved procedures and Cipla policies for document review.
    • Identify and address queries/problems during the review process to prevent delays.

    IV. Issue Documents:

    • Issue documents to applicable units.
    • Maintain records of issuances in the log.
    • Ensure the current version of common documents is available at the unit.

    V. Harmonize and Simplify Documents:

    • Evaluate and prepare documents for standardization across all units at a site.
    • Coordinate with cross-functional teams (CFTs) to simplify processes.
    • Provide suggestions for work simplification and process improvement.


    • Education: M.Sc. / B. Pharma
    • Relevant Work Experience: 1-3 years of experience in the Quality Control department of a pharmaceutical organization.


    • Communication Skills (clarity of thought, comprehension)
    • Potential for growth
    • Job / Product / Technical Knowledge / Pharma domain knowledge
    • Presentation & Interpersonal skills (If applicable)
    • Managerial or People Management skills
    • Safety awareness (If applicable)
    • Comprehension, Analytical & Problem-solving abilities
    • Productivity & Result Orientation (If applicable)
    • Attitude
    • Qualification fitment
    • Sales drive (If applicable)
    • Personality traits (Individualistic / Team player, Outspoken, Maturity level, etc.)

    Job Location: Goa


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