More

    MSN Laboratories Hiring Pharma For Executive Role – Apply on Pharmanika

    BPharma Job Openings at MSN Laboratories – Apply on Pharmanika

    Job Title

    Production Executive

    Company: MSN Laboratories

    Location: Hyderabad, Telangana (On-site)
    CTC / Base Salary: ₹3.10 LPA – ₹4.50 LPA (depending on experience and fit)

    Experience: 3 – 6 years in pharmaceutical production / API / formulation manufacturing

    Employment Type: Full-time (Permanent) — 6 months probation

    Job Summary

    As a Production Executive at MSN Laboratories you will be responsible for day-to-day execution of manufacturing operations for assigned product lines/batches while ensuring compliance with GMP, site SOPs and safety standards. You will coordinate with Quality, Stores, Engineering and Packaging teams to ensure timely release of batches, maintain accurate batch documentation, and drive process adherence and continuous improvement to meet production targets and quality metrics.

    Key Responsibilities

    1. Batch Execution & Manufacturing Operations – Execute manufacturing activities for assigned batches as per Batch Manufacturing Records (BMR/BPR) and work instructions. – Ensure correct weighing, charging, mixing, reaction, filtration, drying, granulation, compression, coating and other operations relevant to the assigned product line. – Confirm line clearance, equipment readiness and material availability prior to batch start.
    2. Documentation & GMP Compliance – Prepare, review and sign batch records, logbooks, and daily production reports accurately and legibly. – Ensure compliance to GMP, SOPs and regulatory requirements during all production activities. – Raise, document and follow-up deviations, non-conformances and change controls in collaboration with QA.
    3. Quality Coordination – Coordinate sample collection and testing schedules with QC; ensure that production activities are aligned with QC hold/release timelines. – Implement corrective actions from QC/QA findings and support investigations.
    4. Safety, Housekeeping & Environmental Controls – Follow EHS guidelines, ensure PPE usage, and maintain high standards of housekeeping in the production area. – Monitor and report any safety incidents, near-misses and ensure timely closure of any corrective actions.
    5. Equipment & Utilities – Ensure proper operation and cleaning of production equipment per SOPs; coordinate with Engineering for breakdowns and preventive maintenance. – Verify CIP/SIP procedures where applicable and ensure utilities (steam, compressed air, chilled water, HVAC) are adequate for batch operations.
    6. Inventory, Consumables & Material Handling – Coordinate with Stores for timely issue of raw materials, packaging materials and consumables; ensure material handling is per SOP (label checks, sampling, MBR verification). – Maintain minimum stock levels for critical consumables as per production requirements.
    7. Process Improvement & Cost Optimization – Identify and implement small process improvements to improve yield, reduce cycle time or reduce rework. – Support initiatives for waste reduction and cost efficiency.
    8. Teamwork & Leadership – Supervise and train production operators/technicians on daily tasks, GMP and safety practices. – Provide shift handover notes and ensure smooth continuity between shifts.

    Required Qualifications & Skills

    Education: B.Pharm / B.Sc. (Chemistry / Microbiology / Biotechnology) or Diploma in Chemical / Pharmaceutical Technology. (M.Sc / M.Pharm preferred for senior profiles)

    Experience: 3–6 years in pharmaceutical manufacturing (APIs or formulations), with hands-on exposure to batch manufacturing and GMP environment.

    Technical skills: Sound understanding of GMP, SOPs, BMR/BPR, documentation practices, batch release workflow, change control and deviation handling.

    Tools: Comfortable with MS Office (Excel / Word), and exposure to ERP/MES systems is an
    advantage.

    Personal skills: Good communication, attention to detail, problem solving, team orientation and ability to work in rotating shifts.

    Preferred / Desirable

    Experience with continuous improvement tools (5S, Kaizen, lean manufacturing) or familiarity with OEE metrics.

    Prior exposure to API manufacturing, hazardous reaction handling, or handling potent
    compounds.

    Certification in Safety / HAZOP knowledge is a plus.

    Key Performance Indicators (KPIs)

    Batch completion rate on-time (% of batches completed as per schedule)
    Batch yield vs. theoretical yield
    Number of documented deviations per month and closure timeliness
    On-time sample submission to QC and turnaround time for batch release
    Safety incident rate / near-miss reporting
    Adherence to GMP documentation (no. of documentation errors per period)

    Reporting & Work Relationships

    Reports to: Production Manager / Senior Production Officer
    Interacts with: QA, QC, Stores, Engineering / Maintenance, Packaging, Supply Chain and EHS
    teams

    Shift & Working Hours

    Rotational shifts likely (including morning / evening / night shifts) depending on production
    schedules. Willingness to work overtime during campaign releases / urgent schedules is
    required.

    Compensation & Benefits (Indicative)

    Base CTC: ₹3.10 LPA – ₹4.50 LPA (depending on experience and negotiations)
    Performance-linked incentives / variable pay (as per company policy)
    Statutory benefits: Provident Fund, ESI (if eligible), gratuity (as applicable)
    Paid leave, medical insurance, and other benefits as per company policy
    Training & development opportunities

    Probation & Notice

    Probation: 3–6 months (as per company policy)
    Notice Period: As per company standards (typically 1–3 months)

    Sample Interview Process (Indicative)

    HR Screening (Round 1) – CV fit, salary expectations, notice period, basic behavioral questions (virtual/telephonic)

    Technical Interview (Round 2) – Production Manager / SME: technical knowledge, batch
    execution scenarios, GMP / deviation handling (virtual or on-site)

    Final / Management Round (Round 3) – Operations / Site Head: culture fit, compensation
    discussion, offer finalization (virtual or on-site)

    How to Apply: Please submit your CV highlighting relevant production experience, key projects / process improvements handled, and current & expected CTC.

    MSN Laboratories is an equal opportunity employer. Candidates from diverse backgrounds are encouraged to apply.

    CLICK HERE TO APPLY ONLINE

    Related Articles

    LEAVE A REPLY

    Please enter your comment!
    Please enter your name here

    Stay Connected

    42,522FansLike
    21,523FollowersFollow
    32,000SubscribersSubscribe
    - Advertisement -

    Latest Articles