- To allocate manpower.
- Checking cleanliness of area and machines.
- Balance verification
- Verification of Raw materials in granulation.
- To check and monitor the dispensing, granulation and compression activities in the department as per plan.
- To update departmental documents and records.
- To do online completed batches entries and close process orders in SAP system.
- To impart training to the operators and workers and maintain records.
- To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department.
- To give requisition of BMRs to the QA department.
- To check the raw material and packing material availability in SAP.
- Intimate material shortages to planning department.
- To Update KPIs.
- To investigate and find out root cause analysis of any identified problem.
- To report incident to Human resources and safety department.
- To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD.
- To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity.
- To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows and scrap area.
- To improve product quality and productivity.
- To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department.
- To follow Good Manufacturing Practices in the department.
- To maintain quality products and maintain quality norms.
- Ensuring implementation of effective sanitation and hygiene activities at all the levels.
- Ensuring upkeep of area and equipment.
- Imparting training to colleagues / subordinates.
- To raise change control, deviation and CAPA.
- To ensure avoidance of breach of data integrity at all levels.
- To ensure compliance to the safety measures.
- To ensure the cleaning of riser filters as per SOP.
- To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.
- To implement QEHS policy & objectives.
- Ensure use of PPE.
- To ensure compliance to Safety Measures. Implementation and Documentation of ISO 9001:2015, ISO14001:2015 and ISO 45001:2018.
- To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same.
- To ensure work permit system during maintenance activities.
- To implement QEHS continual improvement projects at site and monitor.
- To ensure participation and consultation of worker.
- To ensure disposal of waste.
- Authorised to prevent improper workplace conditions.
- To ensure that preventive maintenance of the machines done by maintenance department.
- To complete monthly production plan.
- To do monthly verification of weighing balances.
- To coordinate to external party to do calibration of instruments as per identified frequencies.
- Authorised for reporting of Hazards, Incident, and accidents and near miss Reporting.
- Authorised to prepare OH&S performance document.
- Authorised to conduct training of workmen related to OHSMS.
Qualifications
B.Pharm
About Us
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal employment opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
About The Team
Piramal Pharma Solutions (PPS)
is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.