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Posted:4 days ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Key Responsibilities:

In-Process (IP) Responsibilities:

  • Perform line clearance and IP checks during manufacturing and packaging activities.
  • Monitor critical process parameters during granulation, compression, coating, filling, and packing.
  • Verify BMR/BPR entries and ensure Good Documentation Practices (GDP).
  • Collect and test in-process samples as per approved specifications.
  • Report and escalate any deviations, non-conformities, or abnormal observations.

Finished Product (FP) Responsibilities:

  • Sample and submit finished product batches for QC testing.
  • Coordinate with the QC department for timely testing and release of finished goods.
  • Ensure FP storage conditions and labeling are as per SOPs.
  • Assist in reviewing batch records and supporting batch release activities.
  • Coordinate with warehousing for approved and rejected batch segregation.

Qualifications:

  • B.Pharm / M.Pharm / B.Sc. / M.Sc. in Chemistry, Microbiology, or relevant field.
  • 13 years of experience in QA or QC, preferably in formulations or oral solid dosage manufacturing.

Key Skills:

  • Good understanding of cGMP, GDP, and regulatory compliance (USFDA, WHO, MHRA, etc.).
  • Knowledge of production processes and quality checkpoints.
  • Strong documentation, observation, and communication skills.
  • Familiarity with QMS tools like deviation, change control, and CAPA (optional but preferred).
  • Ability to work in shifts and in a fast-paced environment.

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Titan Laboratories
Titan Laboratories

Laboratory Services

Science City

150 Employees

40 Jobs

    Key People

  • John Doe

    CEO
  • Jane Smith

    CTO

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