Intas Pharmaceuticals Limited has announced a Walk-In Drive at Ankleshwar for experienced professionals seeking career opportunities in the pharmaceutical manufacturing industry. The recruitment drive is being conducted for Officer / Senior Officer positions in the Production – API Department.

Candidates with B.Sc, M.Sc, or BE qualifications and 3 to 8 years of relevant experience in the Production Department are eligible to attend the walk-in interview. Applicants should have sound knowledge of cGMP norms, laboratory safety, API manufacturing operations, and working practices in regulatory-approved pharmaceutical facilities.

The walk-in interview is scheduled for 12th July 2026 (Sunday) at VITS Shalimar Hotel, Ankleshwar. Interested and eligible candidates should attend the interview with an updated resume and all required educational, experience, and salary-related documents.

Intas Pharmaceuticals Recruitment  – Job Overview

Particulars Details

Company Name

Intas Pharmaceuticals Limited

Recruitment Type

Walk-In Drive

Position

Officer / Senior Officer

Department

Production – API

Qualification

B.Sc / M.Sc / BE

Experience Required

3 to 8 Years in Production Department

Job Location

Valia

Walk-In Date

12th July 2026 (Sunday)

Interview Time

09:00 AM to 05:00 PM

Interview Venue

VITS Shalimar Hotel, Ankleshwar

Official Website

www.intaspharma.com

About Intas Pharmaceuticals Limited

Intas Pharmaceuticals Limited is a leading multinational pharmaceutical formulation development, manufacturing, and marketing company with a presence in more than 85 countries worldwide.

According to the recruitment notification, the company is growing at approximately 20% CAGR, and around 70% of its revenue comes from international markets, particularly highly regulated markets such as the European Union and the United States.

Intas Pharmaceuticals offers career opportunities to professionals interested in working in a global pharmaceutical organization with exposure to regulated manufacturing environments, quality systems, and modern pharmaceutical production practices.

Position and Department Details

Position: Officer / Senior Officer

Department: Production – API

The selected candidates will work in the Active Pharmaceutical Ingredient (API) Production Department and may be responsible for pharmaceutical manufacturing operations, documentation, equipment handling, process monitoring, safety compliance, and adherence to regulatory requirements.

Educational Qualification

Candidates possessing any of the following qualifications can attend the walk-in drive:

B.Sc (Bachelor of Science), M.Sc (Master of Science), or BE (Bachelor of Engineering).

Candidates should ensure that their educational background and professional experience are relevant to pharmaceutical production and API manufacturing operations.

Experience Requirements

Applicants must have 3 to 8 years of experience in the Production Department.

Relevant experience in an API manufacturing facility or regulatory-approved pharmaceutical manufacturing organization may be particularly valuable for these positions.

Required Technical Knowledge and Skills

Candidates attending the interview should have good practical knowledge of pharmaceutical production operations.

Important skills and knowledge areas include cGMP compliance, laboratory and manufacturing safety, Standard Operating Procedures (SOPs), Good Documentation Practices (GDP), API production processes, batch manufacturing records, equipment operation, process monitoring, deviation reporting, and experience working in regulatory-approved manufacturing facilities.

Job Location

Valia

Candidates should carefully consider the job location before attending the recruitment drive.

Walk-In Interview Date and Time

Date: 12th July 2026 (Sunday)

Time: 09:00 AM to 05:00 PM

Candidates are advised to reach the interview venue early to complete registration and document verification procedures.

Walk-In Interview Venue

VITS Shalimar Hotel, Ankleshwar

Applicants should verify travel arrangements and plan to arrive at the venue on time.

Documents Required for the Interview

Candidates should carry an updated resume/CV, educational qualification documents, experience certificates, current employment documents, and salary-related documents.

Carrying original documents along with photocopies may be useful for verification purposes.

Important Instructions for Candidates

Candidates who have appeared for an interview at Intas Pharmaceuticals during the last six months are requested not to apply.

Applicants should have thorough knowledge of cGMP norms and laboratory safety.

Relevant functional experience in a regulatory-approved pharmaceutical facility is required.

Candidates should carry their updated resume along with all educational, experience, and salary documents.

Important Recruitment Disclaimer

Intas Pharmaceuticals Limited has clearly stated that the company does not directly or indirectly charge any fee for job applications, recruitment processing, training, or testing.

Candidates should avoid responding to fraudulent job offers or recruitment communications requesting money.

Why Consider a Career in API Production?

Working in an API Production Department can provide valuable professional experience in pharmaceutical manufacturing, process operations, regulatory compliance, production documentation, equipment handling, and industrial safety.

Professionals with strong experience in regulated API manufacturing facilities may develop career opportunities in production operations, technology transfer, manufacturing excellence, compliance, validation, and production management.

5 Technical FAQs for Intas Pharmaceuticals Production – API Interview

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

Answer: cGMP stands for Current Good Manufacturing Practices. It is a regulatory framework designed to ensure that pharmaceutical products are consistently manufactured and controlled according to established quality standards. In API manufacturing, cGMP requirements cover personnel training, equipment qualification, process control, documentation, cleaning procedures, material handling, deviation management, and prevention of contamination and cross-contamination.

2. What is the difference between a deviation, CAPA, and change control?

Answer: A deviation is an unexpected departure from an approved procedure, specification, or established manufacturing process. CAPA (Corrective and Preventive Action) involves identifying the root cause of a problem, correcting it, and implementing measures to prevent recurrence. Change control is a formal system used to evaluate, approve, implement, and document planned changes that may affect product quality, processes, equipment, facilities, or validated systems.

3. What is the purpose of a Batch Manufacturing Record in API production?

Answer: A Batch Manufacturing Record (BMR) provides complete documentation of the manufacturing history of a specific batch. It includes details about raw materials, equipment, processing steps, operating parameters, in-process checks, yields, deviations, and signatures of responsible personnel. Accurate BMR documentation ensures traceability, regulatory compliance, batch review, and data integrity.

4. How can cross-contamination be prevented in an API manufacturing facility?

Answer: Cross-contamination can be controlled through proper equipment cleaning, validated cleaning procedures, dedicated or appropriately segregated manufacturing areas, controlled material and personnel movement, closed processing systems where applicable, effective HVAC systems, appropriate personal protective equipment, line clearance, proper labeling, and strict adherence to SOPs.

5. What should an API Production Officer do when a critical process parameter goes outside the approved limit?

Answer: The Production Officer should take immediate action according to the approved SOP, place the process in a safe and controlled condition where required, inform the Production Supervisor and Quality Assurance team, document the event, and initiate a deviation investigation. The officer should not make unauthorized adjustments or manipulate records. The batch should be evaluated based on the investigation, impact assessment, established procedures, and Quality Unit decision.

Conclusion

The Intas Pharmaceuticals Walk-In Drive is an opportunity for experienced pharmaceutical professionals seeking Officer and Senior Officer positions in the Production – API Department. Candidates with B.Sc, M.Sc, or BE qualifications and 3 to 8 years of relevant production experience can attend the interview on 12th July 2026 at VITS Shalimar Hotel, Ankleshwar.

Eligible candidates should prepare their technical knowledge of API manufacturing, cGMP, safety, documentation, deviations, CAPA, and regulatory compliance and carry all required documents to the interview.