Formulation Scientist

2 weeks ago

Ahmedabad, India Vasa Pharma Chem Full time

Roles and Responsibilities
- Manufacturing and packing operations of tablet formulation.
- Responsible for cGMP document like: Batch Manufacturing records, in process and finished products test requisitions etc.
- Protocol / SOP / BMR preparation for the New Machines, New Product. Revision of protocol / SOP / BMR whenever required and execution of Protocol / SOP / BMR.
- Responsible for calibration qualification and validation activity of respective equipment for products.
- Make daily reports to R&D manager / superiors on day to day activities concerning the department.
- Coordination with other departments like Admin, Warehouse, QC, QA, QE, MIS and engineering for related activities.
- Maintaining the GMP documents like equipment logbooks, records of physical monitoring and housekeeping records.
- To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established / new procedures, maintaining and updating existing procedures in the department.
- Responsible to co-maintain, coordinate for validation and GMP in all departments along with the Quality Assurance officer and to coordinate with Quality Control department in matters relating to Product Quality.
- Training the subordinates and manpower to meet the organizational goals and achieve GMP compliance.
- Should have fluency in English and presentable.

**Salary**: ₹15,000.00 - ₹30,000.00 per month

Schedule:

- Day shift

Supplemental pay types:

- Performance bonus

Ability to commute/relocate:

- Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 1 year (preferred)

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