Executive- Pharma Packing

Zentiva; Ankleshwar; Presencial; INR 350 000 - 550 000; Tempo integral

Resumo da oferta

Zentiva is seeking an Executive, Pharma Packing in Gujarat for 1–6 years of pharmaceutical manufacturing experience. The role focuses on implementing production schedules, ensuring quality and compliance with GMP, ISO, GQS and HSE guidelines while coordinating with maintenance, procurement, quality and production teams.

SAP activities and team handling are integral parts of the job. Candidate should hold B.Pharm or M.Pharm and be prepared to work across shifts in a packing environment,

Qualificações

• 1-6 years in pharmaceutical manufacturing, preferably in packing.
• Knowledge of GMP, data integrity and regulatory guidelines.
• Experience with SAP-related activities and coordination with multiple departments.

Responsabilidades

• Implement monthly production schedules with quality adherence.
• Ensure compliance with regulatory, GQS, and HSE guidelines.
• Coordinate with Engineering, Purchase, Quality, and Production departments.
• Monitor yield and pursue continuous improvement in assigned products.
• Provide training on GMP, data integrity, and ISO requirements.
• Carry out qualifications/ validations as directed by Dept. Head.
• Identify unsafe conditions and maintain plant assets efficiently.

Conhecimentos

GMP

Formação académica

B.Pharm

M.Pharm

Ferramentas

SAP

Descrição da oferta de emprego

Job Description:

Job Title - Executive, Pharma Packing

Experience

1 to 6 years in pharmaceutical manufacturing (Preferably in Packing )

Education

B.Pharm (Bachelor of Pharmacy) , M.Pharm (Master of Pharmacy)

1. Production

1.1. Implementing monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time.

1.2. Performing the production activities in assigned areas in order to achieve 100 % customer service.

1.3. Performing the SAP related activities

1.4. Able to handle the team consist of Contractual persons ,FTC & Operators in allocated shift

1.5. Able to do troubleshooting in the allocated area

2. ISO 14001 and SAP

2.1. Adhering to ISO 14001 activities and objectives in Pharma Mfg. Performing all the SAP related activities as and when needed.

3. Compliance

3.1. Implementing and ensuring compliance to GQS, HSE and ISO guidelines / standards and maintaining documentation for the same including process validation and qualification.

4. Coordination

• Engineering department for preventive and break down maintenance, modifications etc.


• Purchase department for procuring and controlling auxiliaries.


• Quality department for all quality related matters.


• Production department for bulk availability.

5. Yield monitoring

5.1. Implementing and making efforts for continuous improvement of yield of assigned products

6. Training

6.1. 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.

7. Others

7.1. Carrying out any other assignments or projects like qualifications and validations as per the instruction of the Dept. Head to meet the organizational priorities.

7.2. Identifying and correcting unsafe conditions or behavior and promptly reporting other potentially hazardous situations.

7.3. Maintaining plant assets in good condition and making optimum use of all resources.

7.4. Ready to work in each shift & in any allocated areas