Sr. Executive – Quality Assurance

6 years

0 Lacs

Posted:3 weeks ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

📢 We’re Hiring: Sr. Executive – Quality Assurance (QA)

Location:

Company:

Industry:

highly motivated and detail-oriented Senior Executive – QA



🔍 Key Responsibilities:

  • Prepare, review, and execute 

    Standard Operating Procedures (SOPs)

    .
  • Draft and evaluate 

    process and cleaning validation protocols and reports

    .
  • Review equipment, instrument, and utility 

    qualification protocols and reports

    .
  • Review 

    Site Master File

     and 

    Validation Master Plan

    .
  • Prepare and review 

    Annual Product Quality Review (APQR)

     ensuring critical parameters are trending well.
  • Handle 

    dispatch activities

    , including documentation.
  • Execute 

    QMS-related tasks

     and ensure proper entries in logbooks.
  • Issue and review executed 

    BMRs, ECRs, and logbooks

    .
  • Regularly monitor 

    equipment and instrument calibration

    .
  • Manage 

    finished goods approval, rejection, and batch release

    .
  • Review 

    self-inspection records

     and drive improvements.
  • Maintain 

    approved and provisional vendor lists

    .
  • Timely issue of 

    documents and logbooks

     to relevant departments.
  • Conduct 

    sampling activities

     and verify records.
  • Issue 

    outer labels and seals

     as per requisition slips.
  • Report any product, process, or system-related issues to 

    Head – QA

    .
  • Review and sign 

    Finished Product Protocol and COA

     in absence of 

    Head – QC

    .
  • Approve 

    Finished Product Protocol and COA

     in absence of 

    Head – QA

    .
  • Evaluate 

    training feedback and performance assessments

    .
  • Undertake any other responsibilities assigned by the 

    Head of Department

    .



✅ Ideal Candidate Profile:

  • Bachelor’s/Master’s in Pharmacy, Chemistry, or related discipline.
  • 4–6 years of experience in QA roles in a regulated pharmaceutical environment.
  • Sound knowledge of GMP, documentation, validations, and quality systems.
  • Proficient in cross-functional coordination and QMS activities.
  • Strong attention to detail, documentation, and compliance-driven mindset.



📩 Ready to make an impact?

qa.head@valens.co.in

Let’s ensure quality, compliance, and excellence – together.

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