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Full-time
bachelor degree, postgraduate degree
Posted 26d ago
~40 hrs/week
Responsibilities
Manage monthly production schedules in the granulation, compression, and coating sections while ensuring compliance with GQS, HSE, and ISO standards. Coordinate with engineering, quality, and packaging departments to optimize yield and maintain plant assets.
Requirements
Requires a B. Pharm or M. Pharm degree with 1 to 5 years of experience in pharmaceutical manufacturing. Candidates must be proficient in SAP and capable of working in rotating shifts.
Full job description
Job Title: Executive – Production, Pharma
Educational Qualification and Experience:
M. Pharm / B. Pharm from a reputed university, having 1 to 5 years in pharmaceutical manufacturing (Preferably in Granulation , compression & Coating section)
Key Accountability:
Production
Implementing monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time.
Performing the production activities in assigned areas in order to achieve 100 % customer service.
Performing the SAP related activities
Able to handle the team consist of Contractual persons ,FTC & Operators in allocated shift
Able to do troubleshooting in the allocated area
ISO 14001 and SAP
Adhering to ISO 14001 activities and objectives in Pharma Mfg. Performing all the SAP related activities as and when needed.
Compliance
Implementing and ensuring compliance to GQS, HSE and ISO guidelines / standards and maintaining documentation for the same including process validation and qualification.
Coordination
Coordinating with
Engineering department for preventive and break down maintenance, modifications etc.
Purchase department for procuring and controlling auxiliaries.
Quality department for all quality related matters.
Packaging department for bulk availability.
Yield monitoring
Implementing and making efforts for continuous improvement of yield of assigned products
Training
Impart training to the operative staff (like contractual persons, FTC & operators ) on GMP, Data Integrity ,HSE, ISO requirement & process improvement and maintaining good industrial relation in the plant by effective grievance process.
Others
Carrying out any other assignments or projects like qualifications and validations as per the instruction of the Dept. Head to meet the organizational priorities.
Identifying and correcting unsafe conditions or behavior and promptly reporting other potentially hazardous situations.
Maintaining plant assets in good condition and making optimum use of all resources.
Ready to work in each shift & in any allocated areas
At Zentiva, we provide health and wellbeing for all generations
Industry
Pharmaceutical Manufacturing
Company size
5,001-10,000 employees
Headquarters
Prague 10
LinkedIn followers
114,865
Total funding
$104M
Zentiva provides health and wellbeing for all generations, with focus on developing, producing, and delivering high-quality, affordable medicines to more than 100 million people in over 40 countries across Europe and beyond. Zentiva has four manufacturing sites and a broad network of external manufacturing partners. Zentiva employs more than 5,400 unique talents, bonded together by a commitment to the people who depend on our products every day. Visit us at www.zentiva.com.
Data protection: It’s not just a checkbox – it’s our commitment! Please visit our Privacy Notice https://www.zentiva.com/gdpr/privacy-notice
Offices: U Kabelovny 529/16, Dolní Měcholupy, Prague 10, 102 00, CZ
Generics and OTCHealth CareMedicalManufacturingPharmaceutical
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