Executive - Formulation Technology Transfer

Torrent Pharmaceuticals

Dahej

On-site

INR 500,000 - 1,000,000

Full time

14 days+

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Job summary

Torrent Pharmaceuticals in Dahej is seeking an Executive for their FTT department with 3 to 8+ years of experience. The role includes responsibilities such as supervising Technology Transfer activities, ensuring compliance with all quality and safety standards, and maintaining production documentation. Candidates must hold a B. Pharm. or M. Pharm. degree and have OSD pharmaceutical experience. Interested candidates can share their updated CV via email.

Qualifications

Candidates should have in-depth experience in FTT department.
Experience in OSD pharmaceuticals is mandatory.

Responsibilities

Receive instructions from AM / Manager / GM and plan work accordingly.
Track daily product manufacturing progress.
Organize and supervise Technology Transfer department activities.
Ensure compliance with Quality, Health, Safety, Environment policies.
Prepare documents for New Product and site shift products.

Skills

In-depth experience in FTT department

OSD pharmaceutical experience

Communication skills

Knowledge sharing

Education

B. Pharm. / M. Pharm.

Job description

Roles & responsibilities

To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head.

To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor its progress constantly.

To organize, supervise and control the activities of Technology Transfer department.

To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department.

To check and update various documents and records, ensure production records filled online during batch manufacturing.

To check and maintain housekeeping of the department. To enforce latest developments in GMP, SOP's etc.

To observe and report to the seniors of Product / Material / Machine for their abnormal identified behaviour during production process.

To counter check Raw Materials Dispensing and to recheck the material prior to their use in production processes.

To ensure that the Quality, Health, Safety, Environment policy and procedures are followed.

To prepare documents of New Product (ANDA) and site shift products (which includes CCF, MFC, BMR, QFR, ISP, PPQP, QRM, ESR TT Protocol, TT Report & PPQR (not limited to).

To prepare documents for MES activity.

To check, (i) Sampling request to Quality Assurance Department (ii) Material requirements requisitions (iii) Received batch from RM department

To check / verify, (i) Daily Work in progress status.

To achieve required production targets as per the budgetary norms.

Handling of change parts. To ensure proper follow of company's rules and regulations.

To ensure that all documents are complete in all respect prior to next stage of processing.

To write requisition slips of Auxiliary Materials / Stationary materials etc. of daily use.

To procure and control the utilization of such materials.

To maintain optimum stock level of such materials for smooth functioning of department.

To carry out any additional responsibility entrusted from time to time.

Monitoring of Production process at each stage.

To understand and follow all written procedure and manufacturing instructions mentioned in the respective batch record or any other quality document before starting production activity.