Mepro Hiring QA, QC, Regulatory Affairs & Production

Mepro Pharma Hiring | QA QC Production Jobs

Mepro Pharmaceuticals hiring for QA, QC, Regulatory Affairs & Production roles. B.Pharm, M.Pharm, B.Sc, M.Sc candidates eligible.

Mepro Pharmaceuticals Pvt. Ltd. has announced multiple pharmaceutical job openings for Quality Control, Quality Assurance, Regulatory Affairs, Microbiology, and Production departments at its Unit-III facility in Vadodara, Gujarat. Candidates searching for pharma manufacturing jobs, QA officer vacancies, QC analyst jobs, microbiology openings, regulatory affairs careers, and OSD production opportunities can apply for these latest pharmaceutical industry openings.

The company is hiring candidates across Junior Officer to Assistant Manager and Deputy Manager positions for multiple regulated pharmaceutical departments. Candidates with B.Pharm, M.Pharm, B.Sc, and M.Sc qualifications who are interested in pharmaceutical quality systems, manufacturing operations, microbiology testing, dossier preparation, GMP compliance, and pharmaceutical production are encouraged to apply.

These openings are ideal for professionals seeking long-term careers in pharmaceutical manufacturing, quality assurance, analytical quality control, microbiology laboratories, regulatory affairs, and OSD production operations.

Company Overview

Mepro Pharmaceuticals Pvt. Ltd. is a growing pharmaceutical manufacturing company committed to delivering quality healthcare products while maintaining strong compliance with pharmaceutical manufacturing standards. The organization focuses on regulated manufacturing systems, quality-driven operations, and continuous improvement across pharmaceutical production and quality functions.

The company operates advanced manufacturing facilities with strong emphasis on GMP compliance, quality management systems, regulatory documentation, pharmaceutical production excellence, and employee growth.

Mepro Pharmaceuticals continues to strengthen its workforce by hiring experienced pharmaceutical professionals for Quality Control, Quality Assurance, Production, Microbiology, and Regulatory Affairs departments.

The company offers a professional work environment, career development opportunities, employee-focused policies, and exposure to pharmaceutical manufacturing operations aligned with regulatory standards.

Job Role & Responsibilities

Quality Control Department

Available Position

• Junior Officer to Assistant Manager

Experience Required

• 1 to 10 Years

Qualification Required

• B.Sc
• M.Sc

Key Responsibilities

• Perform sampling and analysis of raw materials, packing materials, in-process samples, finished products, and stability samples
• Handle QC instruments including HPLC, GC, UV, IR, and Dissolution systems
• Support analytical documentation and data review activities
• Conduct OOS and OOT investigations
• Participate in calibration and regulatory compliance activities
• Support audit preparation and quality documentation systems
• Manage analytical sections and laboratory operations effectively

Candidates with strong analytical chemistry exposure and pharmaceutical QC experience may receive preference.

Quality Assurance Department

Available Position

• Junior Officer to Assistant Manager

Experience Required

• 1 to 10 Years

Qualification Required

• B.Pharm
• M.Pharm

Key Responsibilities

• Handle IPQA, QMS, Validation, Documentation, and Compliance activities
• Review BMR, BPR, SOPs, protocols, deviations, CAPA, and change control documents
• Support qualification and validation activities
• Ensure compliance with GMP and pharmaceutical quality standards
• Participate in internal and external audit activities
• Maintain regulatory documentation and compliance systems
• Coordinate with manufacturing and quality teams

Candidates with expertise in pharmaceutical quality systems and documentation management may receive preference.

QC Microbiology Department

Available Position

• Junior Officer to Senior Executive

Experience Required

• 2 to 5 Years

Qualification Required

• B.Sc
• M.Sc

Key Responsibilities

• Perform environmental monitoring and water testing activities
• Conduct microbial analysis and sterility testing
• Handle microbial culture preparation and media preparation activities
• Maintain microbiology documentation and investigation records
• Ensure compliance with regulatory microbiology standards
• Support audit preparation and microbiological compliance systems

Candidates with microbiology laboratory exposure and pharmaceutical sterile testing knowledge may receive preference.

Regulatory Affairs Department

Available Position

• Junior Officer to Deputy Manager

Experience Required

• 2 to 15 Years

Qualification Required

• B.Pharm
• M.Pharm

Key Responsibilities

• Prepare and review pharmaceutical dossiers and registration documents
• Handle variation filings, renewals, and regulatory submissions
• Coordinate with regulatory authorities and compliance teams
• Support query responses and product registration activities
• Ensure compliance with market-specific regulatory guidelines
• Maintain documentation related to pharmaceutical licensing and approvals

Candidates with regulatory submission experience and dossier preparation expertise may receive preference.

Production – OSD Department

Available Position

• Junior Officer to Executive

Experience Required

• 2 to 5 Years

Qualification Required

• B.Pharm
• M.Pharm

Key Responsibilities

• Handle granulation, compression, coating, capsule filling, and packing activities
• Operate pharmaceutical manufacturing equipment and machines
• Perform line clearance and documentation activities
• Manage manpower allocation and production schedules
• Ensure compliance with GMP and manufacturing SOPs
• Coordinate production activities with QA and Warehouse teams
• Support smooth pharmaceutical manufacturing operations

Candidates with OSD production exposure and regulated manufacturing experience may receive preference.

Eligibility / Qualifications

Candidates interested in these pharmaceutical vacancies should possess relevant educational qualifications and pharmaceutical industry experience.

Required Educational Qualification

Eligible candidates should possess:

• B.Pharm
• M.Pharm
• B.Sc
• M.Sc

Relevant Courses

B.Pharm, M.Pharm, B.Sc Chemistry, M.Sc Chemistry, Microbiology, Pharmaceutical Analysis, Industrial Pharmacy, Pharmaceutical Quality Assurance, Pharmaceutical Manufacturing, Regulatory Affairs, Pharmaceutical Technology, Analytical Chemistry, Clinical Research, GMP Compliance, Validation, Quality Management Systems, Pharmaceutical Documentation

Experience Requirement

• Experience ranges from 1 to 15 years depending on department and designation
• Pharmaceutical manufacturing experience is preferred
• Candidates with regulated pharma industry exposure may receive preference

Preferred Skills

• HPLC, GC, UV, IR, and Dissolution handling
• IPQA and QMS activities
• Validation and qualification exposure
• Regulatory dossier preparation
• OSD manufacturing operations
• Environmental monitoring and microbiology testing
• Documentation and audit support
• GMP and regulatory compliance understanding

Candidates searching for pharma jobs in Vadodara, QA officer jobs, QC analyst careers, regulatory affairs openings, microbiology vacancies, and OSD production jobs can apply for these pharmaceutical industry positions.

Location & Salary

Job Location

Vadodara

Salary

Salary will be offered according to candidate experience, qualification, technical expertise, and pharmaceutical industry standards.

Application Process

Interested and eligible candidates can apply through the company recruitment process.

Company Address

Mepro Pharmaceuticals Pvt. Ltd. (Unit-III) 141/2 & 227, Haripura, Jarod, Samlaya Road, Ta-Savli, Dist-Vadodara-391520, Gujarat

Application Process

Candidates can apply through the company recruitment portal or official application process mentioned by the organization.

Documents Required

Candidates should keep the following documents ready:

• Updated Resume/CV
• Educational Certificates
• Experience Certificates
• Government ID Proof
• Passport Size Photographs
• Latest Salary Details

Applicants with pharmaceutical manufacturing and regulatory compliance experience may receive preference during the selection process.

Why Join Mepro Pharmaceuticals?

• Strong career growth opportunities
• Professional pharmaceutical manufacturing environment
• Exposure to regulated quality systems
• Employee-focused work culture
• Opportunities in QA, QC, Production, and Regulatory Affairs
• Long-term career stability in pharmaceutical manufacturing

FAQs

1. Which departments are hiring at Mepro Pharmaceuticals?

The company is hiring for Quality Control, Quality Assurance, QC Microbiology, Regulatory Affairs, and Production OSD departments.

2. What qualifications are required for these pharma jobs?

Candidates with B.Pharm, M.Pharm, B.Sc, and M.Sc qualifications are eligible depending on the department.

3. What experience is required for these openings?

Experience requirements range from 1 to 15 years depending on the department and designation.

4. What analytical instruments experience is preferred for QC roles?

Candidates with HPLC, GC, UV, IR, and Dissolution instrument handling experience may receive preference.

5. What skills are preferred for QA and Regulatory Affairs roles?

Candidates with expertise in QMS, CAPA, validation, documentation, and dossier preparation are preferred.

6. Where is the job location?

The job location is Vadodara, Gujarat.

Summary Table

Company	Mepro Pharmaceuticals Pvt. Ltd.
Department Vacancies	QC, QA, QC-Microbiology, Regulatory Affairs, Production-OSD
Qualification	B.Pharm, M.Pharm, B.Sc, M.Sc
Experience	1 to 15 Years
Location	Vadodara