13 - 16 years

12 - 15 Lacs

Posted:1 day ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Position:

Location:

Reports To:

Department:

About KCIL Specialty Chemicals

innovation, quality, and sustainability

5 strategic manufacturing locations in Taloja

continuous improvement, investing in people, and fostering a work culture that rewards performance, innovation, and collaboration

Role Objective

Quality Assurance (QA) and Quality Control (QC)

Key Responsibilities

1. Quality Assurance (QA)

  • Develop, implement, and maintain Quality Management Systems (QMS), SOPs, and quality policies.
  • Ensure compliance with

    GMP, ISO, REACH, BIS, FDA, NABL

    , and other applicable regulations.
  • Lead and manage

    internal, external, and customer audits

    including Eco Vadis and carbon footprint audits.
  • Ensure accuracy of critical documentation such as:
    • Batch Manufacturing Records (BMRs)

    • Change Control requests

    • Deviation reports

    • Corrective and Preventive Actions (CAPA)

  • Oversee product traceability, recall procedures, and customer complaint resolution.
  • Conduct training sessions on

    quality systems, regulatory updates, documentation, and compliance

    .
  • Monitor readiness for statutory inspections and certifications.
  • Drive

    continuous improvement projects

    across all plants.

2. Quality Control (QC)

  • Oversee all QC laboratory activities including

    sampling, testing, and data reporting

    for:
    • Raw Materials (RM)
    • Packing Materials (PM)
    • Work-in-Progress (WIP)
    • Finished Goods (FG)
  • Approve

    Certificate of Analysis (COA)

    prior to product dispatch.
  • Ensure adherence to

    Good Laboratory Practices (GLP)

    , ISO, BIS, and GMP.
  • Review and maintain documentation as per

    audit and regulatory standards

    .
  • Ensure calibration, preventive maintenance, and availability of critical lab instruments:
    • HPLC, GC, FTIR, UV, GC-MS, ICP-MS

  • Supervise and guide QC Chemists, Analysts, and Lab Technicians.
  • Analyze and interpret test results for compliance, troubleshooting, and decision-making.
  • Investigate quality deviations, perform

    Root Cause Analysis (RCA)

    , and ensure timely CAPA implementation.
  • Manage laboratory consumables, reagents inventory, and manpower planning.
  • Collaborate closely with

    Production, R&D, QA, and EHS

    to resolve quality issues and improve processes.

Job Specification (JS)

Education

  • B.Sc. / M.Sc. in Chemistry (preferably Organic or Analytical Chemistry).

Experience

  • 8 to 12 years in

    Quality Assurance & Quality Control

    in the chemical, pharma, or specialty chemical industry.
  • At least

    3–4 years in a leadership role

    , handling teams and audits independently.

Skills & Competencies

Technical Skills

  • Strong knowledge of

    QA systems, GMP, ISO, REACH, BIS standards

    .
  • Hands-on with analytical instruments (

    HPLC, GC, FTIR, UV, GC-MS, ICP-MS

    ).
  • Experience in handling

    audits

    (FDA, ISO, NABL, REACH, Eco Vadis, customer audits).
  • Proficiency in

    documentation, SOP management, CAPA, Change Control, and RCA

    .
  • Knowledge of

    Statistical Quality Control (SQC)

    and data-driven decision making.
  • SAP / ERP usage (preferred).

Behavioral Competencies

  • Leadership & People Management

    – ability to lead teams of QA/QC professionals.
  • Analytical Thinking

    – structured approach to problem-solving and decision making.
  • Effective Communication

    – articulate in technical and regulatory discussions.
  • Accountability & Ownership

    – ensures end-to-end responsibility for quality.
  • Collaboration

    – ability to influence and work cross-functionally across departments.
  • Attention to Detail

    – meticulous in audits, documentation, and testing.

Additional Requirements

  • Must have experience in

    regulated plants

    with documentation compliance.
  • Prior experience in

    customer audits & regulatory inspections

    is mandatory.
  • Willing to be based

    full-time at Taloja manufacturing location

    .
  • Should be capable of representing KCIL in

    technical discussions with customers and regulators

    .

Growth & Career Path

  • Opportunity to grow into

    Head – Quality / Head – Operations

    based on performance.
  • Exposure to global audits and advanced regulatory compliance (REACH, Eco Vadis, Carbon Audits).
  • Participation in strategic initiatives aligned with KCIL’s vision to double its turnover.

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