NOVARTIS HIRING D. PHARM / B. PHARM CANDIDATES FOR PRODUCTION (GRANULATION) DEPARTMENTS.

 NOVARTIS JOB OPENINGS FOR D. PHARM / B. PHARM CANDIDATES FOR PRODUCTION (GRANULATION) DEPARTMENTS.

ABOUT NOVARTIS:

Novartis International AG is a Swiss multinational pharmaceutical corporation based in Basel, Switzerland. It is one of the largest pharmaceutical companies in the world.Novartis manufactures the drugs clozapine (Clozaril), diclofenac (Voltaren; sold to GlaxoSmithKline in 2015 deal), carbamazepine (Tegretol), valsartan (Diovan), imatinib mesylate (Gleevec/Glivec), cyclosporine (Neoral/Sandimmune), letrozole (Femara), methylphenidate (Ritalin; production ceased 2020), terbinafine (Lamisil), deferasirox (Exjade), and others.

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

JOB DETAILS;

COMPANY: Novartis

INDUSTRY TYPE : Pharma / Healthcare / Clinical research

FUNCTIONAL AREA : Technical Operations.

DEPARTMENTS: Production

POST :Executive Production (Granulation).

QUALIFICATION : D.Pharm / B.Pharm.

EXPERIENCE : 5 to 6 years.

Minimum 5 to 6 years of experience in OSD facility in reputed Pharmaceutical Company handling various equipment and production process.

Operations Management and Execution

Collaborating across boundaries, Functional Breadth

Excellent oral and written English communication skills.

JOB DESCRIPTION:

GMP & abiding and ensuring compliance to the Health, Safety & Environment policy. Ensure compliance with Pharmacopoeia/Group. Requirements /local and International authorities. Completion of all trainings assigned to individuals role. To ensure the integrity of data at workplace. To follow current Good Manufacturing Practices and Good Documentation Practice.

Follow Standard Operating Procedures of Manufacturing and their documents. Maintain cleanliness in the work area, equipment and Machine. To allot & follow up of work as per plan. Co-ordination with cross-functional department. Provide training to new joining associate.

Follow the procedure of miscellaneous material at the time receiving and handling the material. To supervise the work as per allocated job in respective department as per Production norms and Quality norms adhering to Good Manufacturing Practices. Plan & procure the material as per daily production requirement. Filling Batch Manufacturing records.

Maintain the shop floor records; carry out in process checks and record. Co-ordination with engineering department for various maintenance activities. To maintain & ensure compliance at shop floor. To handle associates in the shift, their work allocation & target allocation for the shift. To prepare protocol reports for deviations, quality events & for track wise actions. To conduct trainings of associates at shop floor.

Change control, Quality Event and deviation handling as per SOP. To raise CR and Deviation in track wise and support in investigation and implementation of CAPA. To handle MES.

LOCATION : Mumbai

End Date : 10th May, 2022.

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