Pfizer Walk-In Drive for Freshers & Experienced | Manufacturing Jobs at Vizianagaram | Apply on 25th July 2026

Pfizer Healthcare India Private Limited has announced a Walk-In Drive for Freshers and Experienced Manufacturing Professionals. This recruitment drive offers excellent career opportunities in sterile injectable manufacturing for candidates with qualifications such as Diploma in Pharmacy, Diploma in Chemical, Diploma in Mechanical, B.Pharm, M.Pharm, M.Sc, and B.Sc.

The walk-in interview will be conducted on Saturday, 25th July 2026, at Hotel SVN Lake Palace, Vizianagaram, Andhra Pradesh.

Pfizer Walk-In Drive 2026 Overview

Particular Details

Company Name

Pfizer Healthcare India Private Limited

Job Type

Walk-In Interview

Industry

Pharmaceutical Manufacturing

Department

Manufacturing

Job Location

Visakhapatnam, Andhra Pradesh

Walk-In Date

Saturday, 25th July 2026

Reporting Time

8:30 AM

Interview Venue

Hotel SVN Lake Palace, Vizianagaram

Address

8-12-5, PVS Estates, Lower Tankbund Road, Vizianagaram, Andhra Pradesh – 535003

Available Positions

1. Junior Associate – Manufacturing (Freshers)

Qualification

Diploma in Pharmacy

Diploma in Chemical Engineering

Diploma in Mechanical Engineering

Eligibility

Pass Out Year: 2025 or 2026

Minimum 60% marks

No active backlogs

Job Responsibilities

Operate injectable manufacturing equipment.

Handle sterile production machines.

Perform vial and ampoule filling operations.

Washing, capping and sealing activities.

Compounding operations.

Terminal sterilization.

Visual inspection.

Packing of injectable products.

Follow Current Good Manufacturing Practices (cGMP).

Work with team members to improve production efficiency.

2. Manufacturing Supervisors

Qualification

M.Pharm

M.Sc (Full Time)

B.Pharm

Experience

M.Pharm/M.Sc: 6–10 Years

B.Pharm: 8–12 Years

Required Skills

Injectable Manufacturing (Upstream & Downstream)

USFDA regulated manufacturing experience

Team handling and leadership

cGMP knowledge

Communication skills

Decision-making capability

Manufacturing operations management

3. Manufacturing Experience Operators

Qualification

Diploma

B.Sc

Experience

2–8 Years

Required Experience

Injectable Manufacturing

Vial Filling

Washing

Capping

Sealing

Compounding

Terminal Sterilization

Visual Inspection

Packing Operations

Good Manufacturing Practices (GMP)

USFDA regulatory manufacturing environment

Documents Required

Candidates should carry:

Updated Resume

Government ID Proof

Educational Certificates

Experience Certificates (if applicable)

Last 3 Months Salary Slips

Latest Increment Letter

Why Join Pfizer?

Global pharmaceutical company

Exposure to USFDA-regulated manufacturing

Career growth opportunities

Modern sterile injectable manufacturing facility

Professional work environment

Learning and development programs

Important Instructions

Reach the venue before 8:30 AM.

Carry all original documents along with photocopies.

Freshers must satisfy the eligibility criteria.

Experienced candidates should have relevant injectable manufacturing experience.

Dress professionally for the interview.

5 Technical FAQs

1. What is cGMP and why is it important in pharmaceutical manufacturing?

Current Good Manufacturing Practices (cGMP) are quality standards that ensure pharmaceutical products are consistently produced and controlled according to regulatory requirements for safety, quality, and efficacy.

2. What is terminal sterilization?

Terminal sterilization is the process of sterilizing a pharmaceutical product in its final sealed container using validated methods such as steam sterilization to eliminate microorganisms.

3. What is visual inspection in injectable manufacturing?

Visual inspection involves checking injectable vials or ampoules for defects such as particles, cracks, discoloration, improper filling, or container damage before packaging.

4. What is the difference between upstream and downstream manufacturing?

Upstream manufacturing includes preparation of raw materials and formulation processes, while downstream manufacturing covers filling, sealing, sterilization, inspection, and packaging of finished injectable products.

5. Why is USFDA manufacturing experience valuable?

Experience in a USFDA-regulated facility demonstrates familiarity with strict quality systems, documentation practices, validation, data integrity, and compliance with international pharmaceutical standards.