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3-5 Years
Not Disclosed
Early Applicant
  • Posted 19 days ago
  • Be among the first 10 applicants

Job Description

Purpose - To review documents and monitor manufacture scale up and exhibit batches for smooth transfer of pharmaceutical formulations from R&D to manufacturing site.

Position / Job Title - Sr. Officer/Executive

Department- Technology Transfer

Reporting To - GM- Tech transfer

Location - Pithampur (Madhya Pradesh)

Years of Experience - 3-5 Years

Dosage Form - Solid Orals

Job Responsibilities / Deliverables

  • Documentation

Review batch records like BMR & BPR,

SFG and FG code creation and approval from CFTs

Prepare protocols like process optimization protocol, process evaluation protocol, process validation protocol, hold time protocol, Product transfer protocol

Prepare reports like Process optimization reports, process evaluation reports, process validation report, hold time report, product transfer report

  • Batch Execution

Coordinate and monitor scale-up, exhibit, and process validation batches at the manufacturing site.

Ensure all process parameters, in-process checks, and critical control points are followed as per approved protocols.

Identify process challenges during execution and coordinate with concerned departments for resolution.

  • Coordination & Cross-Functional Support

Act as a center point of contact between R&D, Product Development, Manufacturing, QA, QC, Warehouse, and Engineering for smooth and timely execution of batches.

Arrange all necessary prerequisites, materials, equipment, and utilities prior to batch execution.

Ensure timely communication of project status, deviations, and results to stakeholders.

Cordinate with QC AD team for analytical data of samples collected as per protocol

  • Change Control & Investigations

Initiate, track, and ensure timely closure of Change Controls related to product or process transfers.

Compile and analyze process data required for investigations, deviations, and CAPA activities.

Qualifications & Pre-Requisites

M Pharm (Pharmaceutics)

Knowledge of unit operations involved in manufacturing of solid oral dosage forms i.e. Granulation, Blending, Compression, Coating, Capsulation etc.

Basic knowledge of QMS (change control, deviation etc.)

Additional notes - Role is expected to work in all shifts.

More Info

Job Type:
Industry:
Employment Type:

Key Skills

Capsulation

Product transfer protocol

Process validation report

SFG and FG code creation

Hold time report

Process optimization protocol

Product transfer report

Process evaluation reports

Process evaluation protocol

Process optimization reports

Process validation protocol

Hold time protocol

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