Alivus Life Sciences Limited (Formerly Glenmark Life Sciences) has announced a Walk-in Interview for multiple positions at its API Manufacturing Plant in Dahej, Gujarat. The company is looking for skilled professionals with experience in API manufacturing, Quality Control (QC), and Quality Assurance (QA).

This recruitment offers an excellent opportunity for Diploma, B.Sc., M.Sc., B.Pharm., and B.E. Chemical graduates who want to build their careers with one of India’s leading Active Pharmaceutical Ingredient (API) manufacturers.

Organization Details

Company: Alivus Life Sciences Limited (Formerly Glenmark Life Sciences)

Industry: Active Pharmaceutical Ingredients (API)

Job Type: Walk-in Interview

Plant Location: Dahej, Gujarat

Interview Venue: Alivus Life Sciences Ltd., Plot No. 3109, Ankleshwar GIDC, Ankleshwar, Gujarat – 393010

Interview Date: 03 July 2026 (Friday)

Interview Time: 10:00 AM to 03:00 PM

Available Departments

1. API Production

Qualification

Diploma in Chemical Engineering

B.Sc./M.Sc. Chemistry

Experience

2–6 Years

Required Skills

API Production operations

Reactor handling

Centrifuge operation

Cleanroom equipment handling

cGMP compliance

SOP implementation

2. Quality Control (QC)

Qualification

B.Sc./M.Sc. Chemistry

Experience

2–6 Years

Required Skills

HPLC

Wet Laboratory

Gas Chromatography (GC)

Laboratory Practices

Lab Software

SOP Documentation

Quality Control testing

3. Quality Assurance (QA)

Qualification

B.Sc./M.Sc. Chemistry

B.Pharm.

B.E. Chemical

Experience

1–6 Years

Required Skills

IPQA Activities

Online BMR Review

Cleaning Validation

Line Clearance

API Sampling

Analytical Data Review

Batch Release Support

APQR Preparation

GMP Compliance

Common Eligibility

All candidates should have exposure to:

Regulatory documentation

cGMP guidelines

Pharmaceutical SOPs

Documentation practices

Employee Benefits

Air-conditioned bus transport from Bharuch

One additional leave every month apart from weekly offs

Subsidized bachelor accommodation for employees working near the Dahej API Plant (as per company policy)

Unable to Attend the Walk-in?

Candidates who cannot attend the interview may send their updated resume mentioning:

Total Experience

Current CTC

Expected CTC

Notice Period

Email: Dahej.HR@glenmarklifesciences.com

Selection Process

Walk-in Registration

Document Verification

Technical Interview

HR Interview

Final Selection

Offer & Joining Formalities

Documents Required

Updated Resume

Recent Passport-size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slip

Aadhaar/PAN Card

Any Government Photo ID

About Alivus Life Sciences

Alivus Life Sciences (formerly Glenmark Life Sciences) is a leading manufacturer of Active Pharmaceutical Ingredients (APIs). The company specializes in developing high-value APIs for chronic therapeutic segments and supplies products to several leading global pharmaceutical companies.

Technical FAQs

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

Current Good Manufacturing Practices (cGMP) ensure pharmaceutical products are consistently manufactured and controlled according to quality standards, ensuring product safety, quality, and regulatory compliance.

2. What instruments are commonly used in the Quality Control department?

Quality Control professionals commonly use HPLC, Gas Chromatography (GC), UV-Visible Spectrophotometers, Dissolution Testers, pH Meters, and Wet Laboratory equipment for analysis and testing.

3. What is the role of IPQA in pharmaceutical manufacturing?

In-Process Quality Assurance (IPQA) monitors manufacturing activities in real time, performs line clearance, verifies documentation, checks process compliance, and ensures products meet GMP requirements throughout production.

4. What is APQR in Quality Assurance?

Annual Product Quality Review (APQR) is a comprehensive review of manufacturing, testing, deviations, complaints, stability data, and process performance to verify product consistency and identify improvement opportunities.

5. What is BMR and why is it reviewed?

A Batch Manufacturing Record (BMR) documents every manufacturing step of a batch. Reviewing the BMR ensures all operations, calculations, material usage, and quality checks were completed correctly before batch release.