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Walk-in || Executive , Sr. Executive , Operator , Sr. Operator

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Onsite

Walk-in || Executive , Sr. Executive , Operator , Sr. Operator

HETERO Biopharma

Walk-in || Executive , Sr. Executive , Operator , Sr. Operator

Skills

Compliance

22 days ago

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Important information


Contract type:

Permanent

Salary:

₹300,000 – ₹750,000 / year

Location:

Andra, Andhra Pradesh 535273, India

Work mode:

Onsite

Published on:

1 October 2026

What they need


Key Responsibilities

1. Filling Operations

  • Execute aseptic/non-aseptic filling operations as applicable to the product and manufacturing process.
  • Operate filling machines, filling lines, pumps, conveyors, and associated equipment.
  • Perform line clearance and equipment checks before starting operations.
  • Ensure correct product, components, batch number, and packaging materials are used.
  • Monitor filling parameters such as fill volume/weight, machine speed, pressure, temperature, and other defined process parameters.
  • Perform in-process checks and document results as per approved procedures.
  • Maintain aseptic practices and controlled-area behavior where applicable.
  • Identify and report deviations, equipment abnormalities, contamination risks, and process discrepancies.

2. Packing Operations

  • Perform primary and secondary packing activities according to approved batch packaging records.
  • Operate labeling, cartoning, coding, serialization, inspection, and packing equipment as applicable.
  • Verify packaging components, labels, printed materials, batch details, and expiry dates.
  • Perform line clearance before and after each batch.
  • Ensure reconciliation of packaging materials and finished product.
  • Conduct visual inspection of containers, labels, packs, and finished units.
  • Ensure correct segregation and handling of rejected, damaged, or defective materials.

3. GMP & Documentation

  • Follow current SOPs, Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Work Instructions, and GMP requirements.
  • Complete manufacturing and packaging documentation accurately and contemporaneously.
  • Maintain data integrity in accordance with ALCOA+ principles.
  • Report deviations, incidents, non-conformances, and potential quality risks to the appropriate personnel.
  • Support investigations, CAPA, change controls, and other quality-system activities when required.
  • Ensure proper cleaning, sanitization, and housekeeping of the work area and equipment.

4. Equipment & Maintenance

  • Perform equipment operation and routine checks according to SOPs.
  • Coordinate with Engineering/Maintenance for equipment breakdowns and abnormalities.
  • Assist with equipment cleaning, changeover, setup, and basic troubleshooting.
  • Ensure equipment status labels and logbooks are properly maintained.

5. Safety & Compliance

  • Follow EHS procedures and use appropriate PPE.
  • Handle biological/pharmaceutical materials according to approved safety procedures.
  • Maintain proper waste segregation and disposal.
  • Immediately report safety incidents, spills, equipment hazards, or unsafe conditions.

Key Performance Areas (KPIs)

  • Batch completion within the approved production schedule
  • Right-first-time documentation
  • Compliance with GMP and SOP requirements
  • Filling/packing yield and material reconciliation
  • Reduction of rejects and operational errors
  • Equipment utilization and downtime
  • Deviation and incident compliance
  • Line-clearance compliance
  • Safety performance
  • Audit and inspection readiness

Qualification

For Operator:

  • ITI / Diploma / B.Sc. or equivalent qualification.
  • Experience in pharmaceutical/biopharmaceutical manufacturing is preferred.

For Executive/Officer:

  • B.Pharm / M.Pharm / B.Sc. / M.Sc. / B.Tech. or relevant qualification.
  • Experience in pharma/biopharma manufacturing, filling, or packing is preferred.

Experience

  • Operator: 15 years in pharmaceutical/biopharmaceutical manufacturing or packing.
  • Executive/Officer: 2–6 years in pharma/biopharma production, preferably with filling/packing experience.
  • Experience with aseptic filling, cleanroom operations, vial/syringe filling, visual inspection, labeling, and secondary packing is advantageous.

Required Skills

  • Knowledge of GMP and pharmaceutical manufacturing practices
  • Understanding of filling and packing processes
  • Knowledge of cleanroom and aseptic practices, where applicable
  • Good documentation and communication skills
  • Basic troubleshooting and problem-solving ability
  • Attention to detail
  • Ability to work in shifts
  • Teamwork and cross-functional coordination
  • Understanding of data integrity and ALCOA+ principles

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