Mankind Pharma, one of India’s leading pharmaceutical companies, has announced a Walk-In Recruitment Drive for its biotechnology operations in Vadodara, Gujarat. The company is inviting experienced professionals and fresh talent for multiple openings in Production (Upstream & Downstream), Quality Assurance (QMS), Validation, and Engineering Maintenance departments.

This hiring drive offers an excellent opportunity for candidates looking to build a career in the rapidly growing biotechnology and biopharmaceutical manufacturing sector.

Walk-In Interview Details

Company: Mankind Pharma

Interview Type: Walk-In Drive

Walk-In Dates: 13th & 14th June 2026

Time: 10:00 AM to 5:00 PM

Job Location: Vadodara, Gujarat, India

Interview Venue

The Fern Residency Vadodara, Series by Marriott

Station Road, Near Central Bus Depot, Near S.T. Depot,

Sayajiganj, Vadodara, Gujarat – 390002

Open Positions

Production Department

Executive – Upstream

Experience: 4–5 Years

Qualification: M.Sc Biotechnology / M.Sc Microbiology

Key Responsibilities:

Media preparation

Bioreactor preparation

Cell culture operations

Sample processing

Documentation and compliance activities

Executive – Downstream

Experience: 4–5 Years

Qualification: M.Sc Biotechnology / M.Sc Microbiology

Key Responsibilities:

Chromatography operations

TFF (Tangential Flow Filtration)

Buffer preparation

Bioreactor and culture monitoring

Documentation and QMS activities

Assistant Manager – Downstream

Experience: 4–5 Years

Qualification: M.Sc Biotechnology / M.Sc Microbiology

Key Responsibilities:

Purification and filtration processes

SOP implementation

Daily activity management

Team supervision and documentation

Technician – Downstream

Experience: 0–2 Years

Qualification: B.Sc Chemistry

Responsibilities:

Technical support for downstream production operations

Quality Assurance Department

Sr. Officer – QMS

Experience: 1–3 Years

Qualification: B.Pharm / M.Pharm

Key Responsibilities:

Master document management

Change control

CAPA handling

Deviation management

Training coordination

APQR and QRM activities

Validation Department

Executive – Validation

Experience: 1–3 Years

Qualification: B.Pharm / M.Pharm

Key Responsibilities:

Equipment qualification

Process validation

Cleaning validation

Hold time studies

Computer System Validation (CSV)

Engineering Department

Fitter / Operator (Maintenance)

Qualification: ITI Fitter

Experience: 2–4 Years

Responsibilities:

Maintenance support for biotech and injectable facilities

Boiler Operator (Maintenance)

Qualification: ITI Fitter

Experience: 2–4 Years

Responsibilities:

Boiler operations and utility maintenance in biotech/injectable manufacturing facilities

Why Join Mankind Pharma?

Work with one of India’s most trusted pharmaceutical companies.

Exposure to advanced biotechnology and biopharmaceutical manufacturing.

Career growth opportunities across production, QA, validation, and engineering functions.

Strong focus on quality systems and regulatory compliance.

Professional work environment with continuous learning opportunities.

Documents to Carry

Candidates attending the walk-in drive should carry:

Updated Resume/CV

Recent Passport Size Photographs

Educational Certificates

Experience Certificates

Latest Salary Documents

Government Photo ID Proof

Technical FAQs

1. What is the role of an Upstream Production Executive in a biotech facility?

An Upstream Executive manages media preparation, cell culture development, bioreactor setup, fermentation processes, and monitoring of biological production systems before product harvesting.

2. What is Tangential Flow Filtration (TFF) used for in downstream processing?

TFF is a membrane filtration technique used for concentration, purification, and buffer exchange of proteins, antibodies, and biological products while minimizing membrane fouling.

3. Why is Process Validation important in pharmaceutical manufacturing?

Process Validation ensures that a manufacturing process consistently produces products meeting predetermined quality specifications, regulatory requirements, and patient safety standards.

4. What is CAPA in Quality Management Systems?

CAPA (Corrective and Preventive Action) is a systematic approach used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence of quality issues.

5. What is the purpose of Computer System Validation (CSV)?

CSV verifies and documents that computerized systems used in pharmaceutical manufacturing perform accurately, reliably, and consistently while meeting regulatory compliance requirements such as GMP and data integrity standards.