Anthea Pharma Private Limited, a USFDA-approved sterile injectable manufacturing facility located in Hyderabad, Telangana, has announced a Walk-In Interview Drive for the Microbiology Department. The company is looking for talented and motivated microbiology professionals for Officer and Trainee positions. Candidates with experience in sterile injectable manufacturing and microbiological testing are encouraged to attend this recruitment drive.

This is an excellent opportunity for candidates seeking a career in one of India’s rapidly growing pharmaceutical organizations specializing in sterile injectable products.

Company Overview

Company Name: Anthea Pharma Private Limited

Facility: USFDA Approved Sterile Injectable Manufacturing Facility

Location: Hyderabad, Telangana

Anthea Pharma is known for its advanced sterile injectable manufacturing capabilities and commitment to global quality standards. The company focuses on maintaining stringent microbiological control and regulatory compliance.

Walk-In Interview Details

Department: Microbiology

Interview Date: 19th June 2026

Time: 09:00 AM to 12:00 PM

Job Location: Hyderabad, Telangana

Available Positions

1. Officer – Microbiology

Qualification

M.Sc. Microbiology

M.Sc. Biochemistry

M.Sc. Biotechnology

Experience

02 to 03 Years

Required Skills

Water sample analysis

In-process Bioburden testing

BET (Bacterial Endotoxin Test) analysis

MLT analysis of raw materials and packing materials

Antibiotic assay using microbial methods

Sterility testing

Environmental monitoring in sterile injectable facilities

Preparation and trending of Environmental Monitoring (EM) data

Method validation for Bioburden, BET, and MLT

Preparation of microbiology reports and trend analysis

2. Trainee – Microbiology

Qualification

B.Sc. Microbiology

M.Sc. Microbiology

Biochemistry

Biotechnology

Experience

01 to 02 Years

Required Skills

Environmental monitoring in sterile injectable facilities

Water sample analysis

In-process Bioburden analysis

BET analysis

MLT analysis of raw materials

Packing material microbiological testing

Preparation of microbiological trends and reports

Employee Benefits

Anthea Pharma offers several benefits to selected candidates:

Subsidized canteen facility

Transportation facility

Immediate joining preference

Opportunity to work in a USFDA-approved sterile injectable facility

Exposure to advanced microbiological testing and compliance systems

Note: Male candidates are preferred as per the recruitment notification.

Interview Venue

Anthea Pharma Private Limited

Plot No. 290, Sy. No. 219 & 183,

Pashamylaram, Patancheru Mandal,

Sangareddy District, Telangana – 502307

Contact Details

Website: www.antheapharma.com

Telephone: 08455 696000

Email: recruitment@antheapharma.com

Why Join Anthea Pharma?

Working at Anthea Pharma provides professionals with an opportunity to gain hands-on experience in a globally regulated sterile injectable manufacturing environment. Employees get exposure to microbiological quality systems, regulatory compliance, environmental monitoring programs, sterility assurance practices, and advanced laboratory techniques essential for career growth in the pharmaceutical industry.

Technical FAQs

1. What is Bioburden testing in pharmaceutical manufacturing?

Bioburden testing determines the number of viable microorganisms present in a sample before sterilization. It is a critical quality control parameter used to evaluate contamination levels in raw materials, water systems, and manufacturing processes.

2. What is BET (Bacterial Endotoxin Test)?

BET is a microbiological test used to detect endotoxins produced by Gram-negative bacteria. It ensures injectable products are safe and free from pyrogenic contamination before release.

3. Why is Environmental Monitoring important in sterile facilities?

Environmental Monitoring (EM) helps assess the microbiological quality of cleanrooms by monitoring air, surfaces, personnel, and equipment. It ensures compliance with GMP requirements and maintains sterile manufacturing conditions.

4. What is MLT (Microbial Limit Test)?

MLT is performed to determine whether non-sterile pharmaceutical products meet predefined microbial specifications. It evaluates total microbial counts and checks for specified objectionable organisms.

5. What is Sterility Testing and why is it required?

Sterility testing verifies that sterile pharmaceutical products are free from viable microorganisms. It is a mandatory quality control test for injectable products and is performed according to pharmacopeial requirements such as USP, EP, and IP.