Senior Officer
- 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
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
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.
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
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.
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
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
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
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
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
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

