Milan Laboratories Walk-in drive 6th August 2023 Freshers & Experience for Multiple Positions

Job responsibilities:

1.Maintaining production equipment in proper condition for effective use.

2. To keep a check on productivity & ensure good quality of product.

3.Execution of Production Planning.

4. Maintaining Good manufacturing practices.

5.All Online Documentation checking.

6. Assist in Process Validation & cleaning validation.

7.Assist in Equipment Qualification.

8. Responsible for preparation of Annual Product Quality Review.

9.Working as per approved SOPs.

10. To keep a check on productivity & ensure good quality of product.

11. Reports to Production In charge of Respective Department.

12.Responsible for Personal Hygiene & factory discipline.

Greetings from Milan Laboratories (India) Pvt. Ltd.!!
We are hiring for Engineering and Maintenance department at our Dahej factory.
Below are the requirements:

  • Qualification: B.E./ME in electrical/Mechanical
  • Experience: Total 13-14 years experience in pharmaceutical engineering and maintenance section, having good knowledge of projects, pharma equipments with 21 CFR compliance, good in QAMS documentation.
  • Vacancies: 1


  • Execute all Utility Plant and verify log sheet parameters of Boiler plant, Chiller, Air Compressor, Hot water generation, Water System and HVAC system and Electrical system.
    • Responsible for Preparation and execution of SOP of all Engineering equipments.
    • Check the log sheet parameters of fire hydrant system and maintain the functionality of the system.
    • Check and verify parameter and working of Electrical system like as switchgear, BMC, transformer, VCB, LT panel, electrical panel, DB and PDB.
    • Responsible for calibration of instruments & preventive maintenance of electrical equipment.
    • Verify preventive maintenance and Break-down maintenance of plant machineries, Utility equipments and machines.
    • Responsible for the qualification (URS, DQ, FAT, SAT, IQ, OQ and PQ) of all utility equipments & plant machineries .
    • Responsible for validation & qualification.
    • Verify the qualification of process equipments.
    • Check qualification records of Utility plants and Production plant equipments.
    • Responsible for Verify & check the execution & maintenance of water system.
    • Responsible to perform Risk Assessment for Engineering & Utility Department and related to plant facilities.
    • Monitor and maintain operating of all equipment parameters as per SOPs and ensure strict compliance with cGEP and safety norms.
    • Maintain documentation and other audit compliance matters for Engineering & Utility department
    • Check equipments, connected accessories, and operate them as per the process with safety norms.
    • Verify & review the all documents of Engineering & Utility department.
    • Responsible for AHU running parameter and Validation record of HVAC system and BMS System operation .
    • To check the electrical energy readings & verify the power factor.

Greetings from Milan Laboratories (India) Pvt. Ltd.!!
We are hiring for Packing Officer for the OSD plant at our Dahej factory.

Below are the requirements:

  • Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm
  • Experience: 2-3 year experience in primary and secondary packing.
  • Vacancies: 3


To monitor productivity of production & Packing equipment and Manpower on daily basis.
To supervise the daily activity production & Packing for quality parameters and cGMP compliance.
To co-ordinate cGMP implementation and compliance in all production & Packing area.
To coordinate preparation of MFR/BMR/BPR/OPV and SOP formats as per QA and cGMP requirement with Department Head.
To co-ordinate activities of new products and to ensure availability of change parts/documentation for new product.
To carry out new product optimization and validation batches.
To co-ordinate for in-house calibration and to monitor validation master plan and calibration.
To coordinate breakdown/preventive maintenance.
To document deviations, to review market complaints and out of specification.
Co-ordination for preparation of IQ, OQ, PQ for production equipment.
To co-ordinate cGMP audits/regulatory audits and internal audits.
To conduct training of all subordinates and workers, whenever applicable, as per SOP and cGMP.

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