Mehta walk‑in R&D, QA, Production

BSc MSc API Jobs Walk‑In | Mehta API Boisar

BSc, MSc API pharma vacancies at Mehta API Pvt Ltd Boisar walk‑in for R&D, QA, Production roles. Freshers to 7 yrs.

Mehta API Pvt. Ltd. is conducting a walk‑in interview for multiple positions across R&D, Production, Quality Assurance, EHS, Microbiology, and Engineering functions at its API pharmaceutical manufacturing facility located in Boisar, Maharashtra. The company is inviting qualified professionals from life sciences, chemistry, and engineering backgrounds to participate in this recruitment drive.

Active Pharmaceutical Ingredient (API) manufacturing plays a critical role in the global pharmaceutical supply chain. APIs are the core chemical compounds used in the formulation of finished medicines. Companies involved in API production must maintain strict Good Manufacturing Practices (GMP), regulatory compliance, and process optimization to ensure product safety and quality.

This hiring drive presents an excellent opportunity for candidates ranging from fresh graduates to professionals with up to 7 years of pharmaceutical industry experience to build careers in regulated pharmaceutical manufacturing environments. Selected candidates will work in key technical areas including chemical research, manufacturing operations, environmental safety, microbiological quality monitoring, and plant maintenance.

Professionals joining Mehta API will gain exposure to API process development, chemical manufacturing systems, quality compliance frameworks, and pharmaceutical production technologies used in global pharmaceutical industries.

Company Overview

Mehta API Pvt. Ltd. is a pharmaceutical manufacturing company specializing in the production of Active Pharmaceutical Ingredients (APIs) for domestic and international pharmaceutical markets. API manufacturing companies supply the essential raw pharmaceutical compounds that are later formulated into finished dosage forms such as tablets, capsules, injections, and syrups.

The pharmaceutical industry relies heavily on high‑quality API manufacturers to ensure medicines meet strict regulatory requirements set by global authorities such as the USFDA, WHO, EMA, and other international regulatory agencies. To meet these expectations, companies invest heavily in research laboratories, modern manufacturing equipment, environmental safety systems, and robust quality assurance frameworks.

Mehta API operates its manufacturing facility in Boisar, Maharashtra, one of India’s rapidly growing pharmaceutical manufacturing clusters. The facility supports research, chemical synthesis, manufacturing operations, microbiology monitoring, engineering maintenance, and regulatory quality systems that ensure pharmaceutical products are manufactured safely and efficiently.

Working with Mehta API provides professionals with exposure to chemical process development, pharmaceutical manufacturing operations, regulatory compliance systems, and industrial pharmaceutical production environments.

Job Role & Responsibilities

Mehta API Pvt. Ltd. is recruiting professionals across several technical and operational departments within its pharmaceutical manufacturing facility.

Research & Development (R&D)

R&D professionals play an important role in developing and optimizing chemical synthesis processes used in API manufacturing.

Key responsibilities include:

• Conducting laboratory research for API process development
• Supporting chemical synthesis and reaction optimization
• Recording experimental observations and maintaining laboratory documentation
• Supporting scale‑up activities for manufacturing processes
• Ensuring laboratory activities comply with regulatory and safety guidelines

R&D teams help pharmaceutical companies improve manufacturing efficiency and develop new pharmaceutical products.

Analytical Research & Documentation (ARD)

Analytical documentation teams ensure accurate record keeping and regulatory documentation management.

Key responsibilities include:

• Maintaining documentation related to analytical and research processes
• Managing data entry and documentation systems
• Supporting regulatory documentation preparation
• Ensuring accurate documentation for laboratory and production activities

Proper documentation ensures compliance with pharmaceutical regulatory guidelines and data integrity standards.

Production – API Manufacturing

Production professionals oversee the manufacturing processes used to produce active pharmaceutical ingredients.

Key responsibilities include:

• Supervising chemical manufacturing processes
• Monitoring plant operations and production parameters
• Maintaining batch manufacturing records
• Ensuring compliance with GMP manufacturing standards
• Supporting process optimization and production efficiency

Production supervisors and executives play a key role in ensuring pharmaceutical compounds are manufactured consistently and safely.

Quality Assurance (QA)

Quality assurance professionals ensure that manufacturing processes comply with pharmaceutical regulatory guidelines and internal quality standards.

Key responsibilities include:

• Reviewing batch manufacturing documentation
• Monitoring GMP compliance across manufacturing operations
• Supporting internal audits and regulatory inspections
• Reviewing quality documentation and reports
• Maintaining pharmaceutical quality management systems

QA professionals ensure that pharmaceutical products meet required quality standards before they move to the next stage of production or distribution.

Microbiology

Microbiology professionals monitor microbial contamination and environmental conditions within pharmaceutical manufacturing facilities.

Key responsibilities include:

• Performing microbiological testing of environmental samples
• Monitoring microbial contamination within production areas
• Supporting environmental monitoring programs
• Maintaining microbiology laboratory documentation

Microbiological monitoring is critical to maintaining sterile and contamination‑free pharmaceutical manufacturing environments.

Environmental Health & Safety (EHS)

EHS professionals ensure that pharmaceutical manufacturing plants operate safely and comply with environmental regulations.

Key responsibilities include:

• Monitoring workplace safety conditions
• Implementing environmental safety policies
• Conducting safety training programs
• Maintaining compliance with industrial safety regulations
• Supporting risk assessment and safety audits

These responsibilities ensure safe operations within chemical and pharmaceutical manufacturing plants.

Engineering & Technical Maintenance

Engineering professionals maintain plant infrastructure and ensure continuous operations of manufacturing equipment.

Key responsibilities include:

• Maintaining HVAC systems and plant electrical systems
• Troubleshooting equipment failures
• Performing preventive maintenance
• Ensuring reliable plant utility operations

Technical maintenance teams play a vital role in maintaining efficient pharmaceutical manufacturing operations.

Eligibility / Qualifications

Mehta API Pvt. Ltd. is seeking candidates with relevant academic backgrounds and pharmaceutical or industrial experience.

Required Educational Background

MSc Chemistry, BSc Chemistry, BSc Life Sciences, MSc Microbiology, BCom, BA, ITI Electrical, ITI Mechanical, Diploma Engineering, ADIS Industrial Safety

Candidates with pharmaceutical API manufacturing exposure will be preferred.

Experience Requirements

R&D Officer

Freshers to 3 Years

R&D Executive

5 to 7 Years

Production Supervisor

3 to 4 Years

Production Executive

6 to 7 Years

QA Senior Officer

4 to 5 Years

EHS Officer

2 to 3 Years

HVAC Technician

2 to 3 Years

Electrician

3 to 4 Years

Microbiology Officer

Freshers

Production Operator

4 to 5 Years

Required Skills

Ideal candidates should demonstrate:

• Knowledge of API manufacturing processes
• Understanding of GMP pharmaceutical standards
• Experience in chemical production operations
• Familiarity with pharmaceutical documentation systems
• Ability to work within regulated manufacturing environments

Candidates from pharmaceutical API industry backgrounds are strongly preferred.

Location & Salary

Job Location

Mehta API Pvt. Ltd.

Gut No. 571, 546, 519 & 520
Village Kumbhavali
MIDC Boisar
Dist. Palghar
Maharashtra – 401506

Boisar is an important pharmaceutical and chemical manufacturing hub that hosts multiple API and formulation manufacturing companies.

Salary

Compensation packages depend on candidate experience, technical expertise, and role responsibilities. Professionals with pharmaceutical API manufacturing experience often receive competitive industry salary packages.

Walk‑In Interview Details

Interview Date

13 March 2026 (Friday)

Interview Timing

11:00 AM to 4:00 PM

Interview Venue

Mehta API Pvt. Ltd.
Gut No. 571, 546, 519 & 520
Village Kumbhavali
MIDC Boisar
Palghar District
Maharashtra – 401506

Documents to Carry

Candidates attending the interview should bring:

• Updated resume or CV
• Educational qualification certificates
• Experience certificates (if applicable)
• Identity proof

Only male candidates are required for the current hiring drive according to company hiring requirements.

Application Process

Interested candidates can attend the walk‑in interview directly at the specified venue. Applicants who want to inquire about the recruitment process may contact the HR team.

Contact Number:

8956468343

Candidates should ensure their resume clearly highlights experience in API manufacturing, pharmaceutical research, production supervision, quality assurance, or microbiology testing.

Why Build a Career in API Manufacturing

Active Pharmaceutical Ingredient manufacturing is one of the most critical sectors of the pharmaceutical industry. API manufacturers supply the essential chemical components used to produce medicines across global healthcare systems.

Professionals working in API manufacturing gain valuable experience in chemical synthesis, process optimization, pharmaceutical quality compliance, industrial safety systems, and regulatory documentation.

Typical career progression may include:

• API Production Executive
• Pharmaceutical Process Development Scientist
• Quality Assurance Compliance Manager
• Chemical Manufacturing Specialist
• Pharmaceutical Plant Operations Manager

With growing global demand for medicines, professionals trained in API manufacturing remain highly valuable across pharmaceutical companies and chemical manufacturing industries.

Frequently Asked Questions (FAQs)

Who can attend the Mehta API walk‑in interview?

Candidates with BSc, MSc, ITI, Diploma, or relevant technical qualifications and pharmaceutical manufacturing experience can attend.

Are freshers eligible for any roles?

Yes. Fresh graduates may apply for R&D Officer and Microbiology Officer roles.

What departments are hiring in this recruitment drive?

The company is hiring for R&D, Production, Quality Assurance, Microbiology, EHS, Engineering, and Documentation roles.

Where is the interview location?

The walk‑in interview will be conducted at the Mehta API manufacturing facility located in Boisar, Maharashtra.

What industry experience is preferred?

Candidates with pharmaceutical API manufacturing experience are preferred.

Job Summary

Company	Mehta API Pvt. Ltd.
Vacancies	R&D Officer, R&D Executive, EHS Officer, ARD Officer, Production Supervisor, Production Executive, QA Sr Officer, Micro Officer, HVAC Technician, Electrician, Production Operator
Required Education	MSc Chemistry, BSc Chemistry, MSc Microbiology, BCom, BA, ITI, Diploma, ADIS
Experience	Freshers to 7 Years