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    Junior Team Member QC Job at Cipla | B Pharm Graduates Apply Now

    Junior Team Member QC Job At Cipla

    The Junior Team Member – QC role is a key position within pharmaceutical quality control, focused on documentation, pharmacopoeia compliance, and cGMP standards. This Quality Control Job opportunity is ideal for early-career QC professionals looking to build strong expertise in SOP management, regulatory documentation, and quality systems. Graduates seeking B Pharma jobs or Pharmacy jobs can apply now.

    Job Details

    • Job Title: Junior Team Member – QC
    • Location: Baddi, Himachal Pradesh, India

    About the Company

    The organization operates in the pharmaceutical manufacturing sector with a strong focus on quality, regulatory compliance, and continuous improvement. The QC function plays a vital role in maintaining documentation accuracy, standardization, and adherence to global pharmacopoeia requirements.

    Educational Requirements

    • B. Pharm

    Key Responsibilities

    • Prepare, update, and review SOPs, specifications, and QC documentation.
    • Ensure timely availability of quality documents to support analytical activities.
    • Review applicable pharmacopoeia, supplements, and amendments for compliance.
    • Monitor and implement pharmacopoeia updates to avoid non-conformances.
    • Review instrument calibration data as per operating documents.
    • Maintain online documentation and deviations using approved systems and formats.
    • Ensure accuracy, authenticity, and integrity of QC documentation records.
    • Issue controlled documents and bound books to units with proper issuance logs.
    • Maintain updated issuance records for documents and formats.
    • Support document harmonization and standardization across site units.
    • Coordinate with cross-functional teams for data collection and document updates.
    • Escalate documentation and compliance issues promptly.

    Skills Required

    • Strong knowledge of QC documentation and GMP requirements.
    • Understanding of pharmacopoeia standards and regulatory compliance norms.
    • Experience with electronic documentation systems and controlled documents.
    • Good coordination and communication skills with cross-functional teams.
    • Attention to detail and strong documentation accuracy.
    • Ability to manage timelines and multiple documentation activities.

    Why This Job Role?

    This Quality Control Job role provides hands-on exposure to pharmaceutical QC documentation, pharmacopoeia compliance, and quality systems. It is an excellent opportunity for professionals with 1–3 years of QC experience to strengthen regulatory knowledge and grow within a structured quality environment. Graduates seeking B Pharma jobs or Pharmacy jobs can apply now.

    CLICK HERE TO APPLY ONLINE

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