Pfizer Career Injectable Manufacturing Junior/Assistant Associates Roles

Pharma Stuff; Visakhapatnam; On-site; INR 400,000 - 600,000; Full time

Job summary

Pfizer Healthcare India Private Limited invites qualified professionals to join their injectable manufacturing team as Junior/Assistant Associates in Visakhapatnam.

The role focuses on operating sterile manufacturing equipment, ensuring GMP-compliant production, and maintaining accurate records. Diploma or BSc with 1–5 years' relevant experience in injectable manufacturing and exposure to USFDA-regulated environments are desirable.

Qualifications

• Diploma or BSc (Full-time) required.
• 1–5 years of experience in an injectable manufacturing facility.
• Hands-on experience in USFDA-regulated environments preferred.

Responsibilities

• Operate and maintain equipment for sterile injectable manufacturing.
• Monitor production to ensure GMP-compliant processes.
• Maintain accurate production records and perform routine equipment maintenance.
• Collaborate with team members to resolve issues and improve efficiency.
• Monitor product quality and ensure regulatory standards are met.

Skills

injectable production processes

sterile environments

detail-oriented

GMP compliance

Education

Diploma or BSc

Job description

Explore exceptional career opportunities with Pfizer, a global leader in the pharmaceutical industry. Pfizer Healthcare India Private Limited invites qualified professionals to join their team in injectable manufacturing as Junior/Assistant Associates.

Job Details: Junior/Assistant Associates Roles

Position: Junior/Assistant Associates - Injectable Manufacturing
Location: Pfizer Healthcare India Pvt Ltd, Visakhapatnam

Eligibility Criteria

• Qualification: Diploma or BSc (Full-time)
• Experience: 1-5 years in an injectable manufacturing facility
• Regulatory Knowledge: Hands-on experience with USFDA-regulated environments and processes is mandatory.

Key Responsibilities

As a Junior/Assistant Associate in Pfizer's injectable manufacturing team, you will:

1. Operate and Maintain Equipment: Work with sterile and injectable machinery, including formulation, filling, sealing, and packing machines.
2. Monitor Production: Ensure that all processes meet Good Manufacturing Practices (GMP) standards.
3. Data Management: Maintain accurate production records and conduct routine equipment maintenance.
4. Collaborate: Coordinate with team members to resolve issues and optimize efficiency.
5. Quality Control: Monitor product quality and adhere to strict regulatory standards.

Skills and Attributes

• Strong knowledge of injectable production processes.
• Familiarity with sterile environments and equipment operation.
• Detail-oriented, with excellent problem-solving and teamwork skills.
• Commitment to maintaining the highest standards of GMP compliance.