Job as Production Specialist at Teva Pharmaceuticals

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.

Post : Production Specialist

Job Description
 Responsible for keep up of Compression, Encapsulation, Coating areas in Production.
Responsible for supervising the Manufacturing activities of Compression, Encapsulation and Coating areas in production.
Should have adequate knowledge on Tablet Compression Machines (FETTE 3200IC, 2200I, P2020, CADMACH, CTX, SEJONG, KILLIAN, MANESTY),Capsule Filling Machine (AF 90T,AF 25T, BOSCH, CHECKWEIGHER) & Tablet Coating Machines (GANSCOATER, AUTOCOATER, ACG COATER, NEOCOATER)
Preparation & Review of SOPs, other documents related to manufacturing area
Handling of SAP Transactions related to manufacturing area
Daily Production planning & execution to achieve production targets in time
Performing batch manufacturing activities as per BMR & SOPs
Co ordination with cross functional department for smooth functioning of production activities
Review of batch manufacturing record & related documents pertaining to batch manufacturing records
Wash area & Material storage areas management
Utilisation of allotted manpower in systematic way for smooth functioning of production department
Responsible for training the second line employees to remain in compliance & should undergo training as per identified training needs
Should follow safety practices in the department to remain in safety compliance
Should maintain the department auditworthy at all times
Should ensure compliance to data integrity as per laid down system and procedure
Should maintain discipline work culture in the department
Should have exposure to Oral Solid Dosage Form & should have faced regulatory inspection (USFDA,MHRA,TGA,MCC,ANVISA,WHO)

Candidate Profile
Bachelor of Pharmacy

Additional Information:
Qualification : B.Pharm
Location :  Goa
Industry Type: Pharma / Healthcare / Clinical research
Functional Area: Production
Last Date: 10th January, 2019

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