Vasudha Pharma Chem Ltd has announced new job openings in its Production Department for eligible male candidates. The company is inviting applications from freshers and experienced professionals with a background in Chemistry. This recruitment drive offers opportunities in Production Operations and Production Documentation at its manufacturing facility in Paravada, Anakapalli, Andhra Pradesh.

Candidates possessing a B.Sc. in Chemistry and relevant technical knowledge are encouraged to apply.

Company Overview

Vasudha Pharma Chem Ltd is a leading pharmaceutical and chemical manufacturing organization engaged in producing high-quality Active Pharmaceutical Ingredients (APIs), intermediates, and specialty chemicals. The company operates advanced manufacturing facilities and follows strict quality, safety, and regulatory standards.

Job Details

1. Production Chemist

Department: Production

Experience: 0–3 Years

Qualification: B.Sc. Chemistry

Key Responsibilities

Operate and monitor chemical reactors and production equipment.

Handle SSR (Stainless Steel Reactors) and GLR (Glass Lined Reactors).

Perform ANFD (Agitated Nutsche Filter Dryer) operations.

Carry out centrifuge operations and process monitoring.

Maintain batch manufacturing records and production documents.

Follow GMP, SOPs, and safety procedures.

Coordinate with QA, QC, and Engineering departments.

Required Skills

Knowledge of reactor handling (SSR & GLR).

Experience with ANFD and centrifuge operations.

Understanding of chemical process manufacturing.

Good documentation practices.

Knowledge of GMP and safety regulations.

Teamwork and communication skills.

2. Production Documentation

Department: Production Documentation

Experience: 0–3 Years

Qualification: B.Sc. Chemistry

Key Responsibilities

Prepare and maintain production records.

Review batch manufacturing documents.

Ensure compliance with SOPs and GMP guidelines.

Coordinate with production and quality teams.

Maintain documentation accuracy and traceability.

Support audit and regulatory requirements.

Required Skills

Strong documentation and record management skills.

Knowledge of pharmaceutical GMP requirements.

Good computer proficiency.

Attention to detail and accuracy.

Ability to work with production teams.

Eligibility Criteria

Qualification

B.Sc. Chemistry

Experience

0–3 Years

Gender

Male Candidates

Department

Production

Location

Paravada, Anakapalli

Industry

Pharmaceutical Manufacturing

Job Location

Paravada, Anakapalli, Andhra Pradesh

How to Apply

Interested candidates can share their updated resume through the following contact details:

Email: hrdu3@vasudhapharma.com

Contact Number: 9966953111

Only shortlisted candidates will be contacted for the interview process.

Why Join Vasudha Pharma Chem Ltd?

Opportunity to work in a reputed pharmaceutical manufacturing company.

Exposure to API and chemical production processes.

Learning opportunities for freshers and young professionals.

Career growth in production and manufacturing operations.

Industry-standard training and development.

Technical FAQs

1. What is a Glass Lined Reactor (GLR) and why is it used?

A Glass Lined Reactor is a chemical processing vessel coated with glass to prevent corrosion and contamination. It is widely used in pharmaceutical and chemical manufacturing for handling corrosive chemicals.

2. What is an ANFD in pharmaceutical production?

ANFD (Agitated Nutsche Filter Dryer) is equipment used for filtration, washing, and drying of chemical products within a closed system, ensuring product quality and safety.

3. What are SSR and GLR reactors?

SSR stands for Stainless Steel Reactor, while GLR stands for Glass Lined Reactor. Both are used for chemical reactions, with GLRs preferred for corrosive processes.

4. Why is production documentation important in pharma manufacturing?

Production documentation ensures product traceability, regulatory compliance, batch consistency, and adherence to GMP standards during manufacturing.

5. What GMP knowledge is required for these positions?

Candidates should understand Good Manufacturing Practices (GMP), SOP compliance, batch documentation, cleanliness standards, safety procedures, and regulatory requirements applicable to pharmaceutical manufacturing.