Macleods Pharmaceuticals Ltd – Urgent Vacancy for Manufacturing / Packing / Quality Assurance

Macleods Pharmaceuticals Ltd, India Fastest growing pharmaceutical company, with a strong R&D and own Bio-equivalence centre, manufacturing sites approved by USFDA & WHO Geneva, ranked among the top pharmaceutical companies with a strength of more than 10,000 employees, presently operating in more than 50 countries worldwide.

Greetings from Macleods Pharmaceuticals ltd!!

Vacancy for Production Officer

Experience – 2 to 6 years

Department: Manufacturing (Production)

Location : Sikkim

Job Description:

  • Monitoring of all GMP activities in compression ,Granulation online filling of batch manufacturing records in area .
  • In process checking of all products parameter during compression And Granulation.
  • Filling of BMR with online printing system And logbook
  • Maintain of Daily Records and Log-Books of respective areas.
  • To ensure compliance of SOP in area.
  • Handling Of Man Power .
  • Performing reconciliation related batch yield and compression and Granulation stage
  • Performing daily verification of weighing balance.
  • Handling of DT Apparatus, Hardness, Friability Apparatus, Vernier caliper.
  • Handling of ERP, batch posting.

Interested Candidates can share their resumes on

Role : Officer / Senior Officer Packing 

Department: Production – Packing

Experience: 2 – 8 Years

Location: Sikkim

Job Responsibility:

  • Handling of OSD Packing activity Monthly and weekly planning and review.
  • Review the Yield and Rejection analysis.
  • On line documentation.
  • Preparation of, BPR, Monthly statement.
  • Area Maintenance.
  • Reviewing of document.
  • System handling

Kindly mail updated CV :

Designation: Quality Assurance Officer / Sr Officer (Injectable )

Department : Quality Assurance 

Experience: 4 – 6 Years

Location: Sikkim

Qualification: B.Pharm/M.Pharm/ M.Sc

Job Responsibility:

  • Perform and Monitor IPQA activities injectable Section.
  • Line clearance at each & every stage of  Store, manufacturing & packaging.
  • On line documentation like BMR, BPR, Log books and routine documents.
  • To monitor the activity of calibrations & verification of IPQA instruments.
  • Actively participation in batch Validation.
  • Checking and maintaining Records as per cGMP requirement.
  • To check for the implementations of SOP in the respective areas.
  • Sampling of regular batches at various stage in manufacturing & packaging.
  • Hold time study samples.

Kindly share your cv on : /


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