Glenmark Pharmaceutical is hiring B. Pharma/ M. Pharma for Production Department – Apply Now

Details of the Glenmark Pharmaceuticals Notification are provided below. Candidates who are interested and qualified may show up for the interview at the designated time and location. An expanding pharmaceutical firm with its headquarters in Mumbai (formerly Bombay), India, is known as Glenmark Pharmaceuticals Limited (Glenmark). The company, which was founded in 1977, specialises in the production and distribution of formulation products and active pharmaceutical ingredients (API) both in India and internationally. It also has a broad and expanding presence in regulated and developing worldwide markets.

Post Name: Assistant Manager – Production ( QMS ) / Assistant Manager – Production
Department: Production
Qualification: B. Pharmacy / M. Pharmacy
Experienced: 7-10 years of relevant experience
Selection Process: The selection will be on the basis of Interview
Mode of Interview: Face to Face
Interview Rounds of Interview: HR

Job Responsibilities (QMS)

1. Execution of daily and monthly plan.
2. Achievement daily and monthly targets with predefined quality parameters Plan and allocate manpower to lines as per requirements
3. Process simplification and performance improvement. Aim to achieve zero deviation and 100% utilization of the resources
4. Coordinate with internal suppliers and customers. •Preparation and review of SOPs, BPRS, Qualification and Validation protocols and documents.
5. Exhibit batch planning.
6. Preparation of QMS documents i.e. Investigation, Change Control •Ensure that the production operations are in compliance with the cGMP standards and the Quality Management System.

Job Responsibilities (Production):

1. Execution of daily and monthly plan
2. Achievement daily and monthly targets with predefined quality parameters
3. Plan and allocate manpower to lines as per requirements
4. Process simplification and performance improvement.
5. Aim to achieve zero deviation and 100% utilization of the resources.
6. Evaluate Change Control/CAPA/Incidents/Deviations and ensure timely closure Preparation and review of SOPs, BPRS, Qualification and Validation protocols/ documents.
7. Exhibit batch planning support to R&D batch execution.
8. Ensure preparation of daily production report.
9. Ensure all time compliance in the production facility

Job Location: Glenmark Pharmaceuticals, Colvale Goa (Unit 2)
Post of date: 24/04/2023

Skills Required:

1. Team handling experience, good interpersonal and communication skill.
2. Good in MS office and use of IT applications.
3. Experience in working in SAP and Track and trace application.

Interested candidates can send their CV to Devas.gavada@glenmarkpharma.com

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