Job Overview
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Date PostedDecember 8, 2022
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Location (State / UT)
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Expiration date--
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Experience3 Years, 8 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities
- To assess project and resource requirements.
- To organize relevant training sessions.
- To determine the quality control standards.
- Responsible for day-to-day production planning and execution as per requirement.
- To supervise and evaluate the performance of production personnel.
- Organizing workflow to meet specifications and deadlines.
- Responsible for staff/ worker distribution, allocation, and arrangement as per production planning.
- Responsible for training new joining persons, chemists, workers, operators, and staff for their respective job.
- Responsible to review, approving, and implementing departmental SOPs as per current guidelines.
- Responsible for monitoring and status of online documentation such as BMRs/ BPRs/ Log books and if any other documents.
- Responsible for monitoring production equipment for their performance and zero breakdowns.
- Responsible for monitoring of all activities carried out in the production and packaging area.
- Responsible for monitoring stage-wise process for product yield.
- Responsible for product quality and improvisation of area and equipment.
- Responsible for audit preparation, execution, and compliance.
- Responsible for monitoring and review of QMS documents, qualification protocols, and other online documents for any implementation of CAPA.
- Responsible to update & maintain online departmental documentation.
- Responsible to conduct internal audit / self-inspection to ensure compliance with cGMP and other regulatory requirements.
- Responsible to inform top management of future requirements of departmental up-gradation necessary for the growth of the organization and to meet regulatory requirements.
- Responsible to coordinate with internal as well as external personnel to maintain the cGMP environment.
- Any other responsibilities assigned by the HOD.
Desired Candidate Profile
- Must have work experience in INJECTABLE and Sterile plants.
- Working experience in handling instruments like Thimonier. Autoclave, PFS, Dual Chamber machine.
- Should have worked in the Aseptic area of the Injectable plant.
- Should be Target Oriented.
Qualification: B.Pharma, M.Pharma