Quality Control Laboratory Manager

1 day ago

Roorkee, Uttarakhand, India BADRIVAS BIOTECH PRIVATE LIMITED Full time ₹ 12,00,000 - ₹ 36,00,000 per year

Company Description

Badrivas Biotech Private Limited is dedicated to delivering high-quality healthcare solutions that positively impact lives. We specialize in manufacturing and distributing trusted pharmaceutical products with a strong emphasis on safety, efficacy, and excellence. Our teams in Production, Quality Assurance, and Quality Control uphold the highest standards at every step of the process. At Badrivas Biotech, we aim to empower health, improve lives, and create a lasting impact within communities through our reliable and innovative offerings.

Role Description

This is a full-time on-site role for a Quality Control Laboratory Manager based in Roorkee, Uttarakhand. The Quality Control Laboratory Manager will oversee the day-to-day operations of the laboratory, implement and monitor quality control processes, ensure compliance with regulatory standards, conduct analytical testing, and provide leadership to laboratory staff. Additional responsibilities include maintaining the functionality of laboratory equipment and collaborating with Quality Assurance teams to maintain high operational standards.

Experience:
10–15 years

Location:
Roorkee, Uttarakhand

Key Roles & Responsibilities:

  • Supervise and manage
    all QC laboratory activities
    — including testing of raw materials, in-process samples, and finished formulations.
  • Strong expertise in HPLC
    operation, troubleshooting, and method validation; experience with systems like
    Agilent and Water.
  • Review and approve analytical data, chromatograms, and test reports ensuring
    data integrity
    and regulatory compliance.
  • Manage analytical techniques such as
    GC, UV, IR, Dissolution, and Karl Fischer titration
    .
  • Ensure compliance with
    GMP, GLP, ICH, WHO, and other regulatory requirements
    .
  • Lead
    OOS/OOT investigations
    , implement
    CAPA
    , and conduct root cause analyses.
  • Prepare and maintain
    SOPs, STPs, validation protocols, and stability data
    .
  • Coordinate with
    QA, Production, R&D, and Regulatory Affairs
    for timely product release and process improvements.
  • Handle and face
    regulatory and customer audits
    , ensuring continual audit readiness.
  • Train, mentor, and evaluate QC staff to maintain technical excellence and productivity.
  • Oversee calibration, qualification, and preventive maintenance of analytical instruments.
  • Drive
    continuous improvement initiatives
    to enhance testing efficiency, accuracy, and compliance.

Required Skills & Competencies:

  • Hands-on expertise in
    HPLC
    and analytical method validation.
  • Sound understanding of
    pharma regulatory guidelines (GMP/GLP/ICH)
    .
  • Experience in
    stability studies, impurity profiling, and release testing
    .
  • Proficiency in
    analytical documentation and LIMS/CDS software
    .
  • Excellent team management, communication, and leadership skills.
  • Detail-oriented with strong problem-solving and audit-handling capabilities.

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