Pharmazone Walk-In QA, QC, RA & Project Manager

Pharmazone Regulatory Affairs Jobs | Ahmedabad

Pharmazone hiring for QA, QC, RA & Project Manager roles in Ahmedabad. Apply for B.Pharm, M.Pharm, M.Sc pharma jobs.

Professionals looking for pharmaceutical quality assurance jobs, regulatory affairs careers, GMP consulting roles, pharma project management openings, and business development opportunities in the pharmaceutical sector now have a strong opportunity with Pharmazone. The company has announced a walk-in interview drive for multiple positions in Ahmedabad for experienced candidates from formulation, regulatory affairs, quality systems, and pharma services backgrounds.

Pharmazone is hiring for several strategic positions including Quality Assurance, Quality Control, Regulatory Affairs, Project Management, and Business Development. Candidates with experience in USFDA, MHRA, EU-GMP regulatory environments and formulation manufacturing operations are strongly preferred.

This recruitment drive is particularly beneficial for pharma professionals seeking regulatory compliance jobs, formulation quality assurance roles, EU market regulatory affairs careers, and pharmaceutical consulting opportunities in India.

Company Overview

Pharmazone is a pharmaceutical consulting and regulatory support organization engaged in GMP compliance, regulatory affairs services, pharmaceutical project management, and formulation-related consulting operations. The company supports pharmaceutical businesses in achieving international regulatory standards and compliance requirements.

The organization works with pharmaceutical manufacturing companies across:

• GMP compliance systems
• Regulatory Affairs support
• Pharmaceutical documentation
• Quality Assurance systems
• USFDA and EU-GMP compliance
• Project management services
• Pharmaceutical business consulting
• Formulation regulatory support

Professionals joining Pharmazone gain valuable exposure to highly regulated pharmaceutical operations and international compliance environments.

The current hiring drive focuses on candidates experienced in:

• OSD manufacturing compliance
• USFDA-approved pharmaceutical plants
• MHRA-regulated environments
• EU-GMP documentation systems
• Small molecule generic products
• Pharma regulatory submissions
• Formulation quality systems

Job Role & Responsibilities

Primary Keyword

Regulatory Affairs Jobs

Pharmazone is recruiting experienced candidates across multiple departments.

GMP – Quality Assurance (Formulation)

Number of Vacancies

• 2 Positions

Qualification

• B.Pharm
• M.Pharm

Experience

• 8 to 10 Years

Key Responsibilities

Selected candidates will be responsible for:

• Managing pharmaceutical Quality Assurance activities
• Ensuring GMP compliance in formulation manufacturing
• Handling documentation review systems
• Monitoring production quality standards
• Supporting audit preparedness
• Managing quality systems in OSD facilities
• Coordinating with manufacturing and regulatory teams
• Maintaining pharmaceutical compliance procedures

Candidates must have prior experience in Oral Solid Dosage (OSD) manufacturing. Experience in OSD plus parenteral manufacturing environments will be an added advantage.

GMP – Quality Control (Formulation)

Number of Vacancies

• 2 Positions

Qualification

• B.Pharm
• M.Pharm
• M.Sc

Experience

• 8 to 10 Years

Key Responsibilities

Quality Control professionals may handle:

• Analytical laboratory operations
• Instrument handling and calibration
• Regulatory laboratory documentation
• Method validation activities
• Stability analysis support
• Pharmaceutical testing procedures
• GMP laboratory compliance
• Regulatory audit preparation

Candidates must have experience working in USFDA, MHRA, and EU-GMP-approved pharmaceutical plants.

GMP – Project Manager

Number of Vacancies

• 2 Positions

Qualification

• B.Pharm
• M.Pharm
• M.Sc

Experience

• 6 to 10 Years

Key Responsibilities

Project Managers will support:

• Pharmaceutical project execution
• Client coordination
• Regulatory project planning
• Cross-functional communication
• Timeline management
• Compliance-based project implementation
• Technical documentation management
• Risk assessment and regulatory planning

Candidates with a strong pharmaceutical project management background are preferred.

Business Development – Pharma Services

Number of Vacancies

• 1 Position

Qualification

• B.Sc
• M.Sc

Experience

• 2 Years

Key Responsibilities

The Business Development role includes:

• Selling pharmaceutical services
• Client relationship management
• Business expansion activities
• Pharma consulting coordination
• Lead generation and client acquisition
• Market research and analysis
• Pharma industry communication

Candidates with prior pharmaceutical services sales experience will be preferred.

Regulatory Affairs – US & EU Market

Number of Vacancies

• 2 Positions

Qualification

• B.Pharm
• M.Pharm

Experience

• 2 to 5 Years

Key Responsibilities

Regulatory Affairs professionals may handle:

• Regulatory dossier preparation
• US market submissions
• EU market documentation
• Small molecule generic filing support
• Compliance documentation review
• Regulatory lifecycle management
• Variation filing support
• Coordination with technical departments

Candidates must have experience in US or EU regulatory markets with exposure to small molecule generics.

Regulatory Affairs – Project Manager (F&D/Micro)

Number of Vacancies

• 1 Position

Qualification

• B.Pharm
• M.Pharm

Experience

• 2 to 5 Years

Key Responsibilities

Selected professionals may support:

• F&D project coordination
• Microbiology-related project support
• Regulatory planning
• Product development coordination
• Documentation tracking
• Compliance review systems

Regulatory Affairs – Project Manager (Biotech APAC/EU)

Number of Vacancies

• 1 Position

Qualification

• B.Pharm
• M.Pharm

Experience

• 2 to 5 Years

Key Responsibilities

Candidates may work on:

• Biotech regulatory projects
• APAC market coordination
• EU compliance systems
• Product registration support
• International regulatory submissions
• Cross-functional project execution

Professionals with biotechnology regulatory exposure will have an advantage.

Eligibility / Qualifications

Pharmazone is inviting applications from experienced pharmaceutical professionals with regulatory, GMP, quality systems, and consulting backgrounds.

Required Educational Qualifications

• B.Pharm
• M.Pharm
• M.Sc
• B.Sc

Relevant Courses

Pharmaceutics, Pharmaceutical Regulatory Affairs, Pharmaceutical Analysis, Pharmaceutical Chemistry, Quality Assurance, Quality Control, Analytical Chemistry, Industrial Pharmacy, Regulatory Sciences, Microbiology, Biotechnology, Pharmaceutical Management, Formulation Development

Preferred Industry Experience

Candidates with the following experience will be preferred:

• USFDA-approved manufacturing plants
• MHRA-regulated pharmaceutical facilities
• EU-GMP environments
• OSD manufacturing units
• Regulatory Affairs operations
• Pharma consulting projects
• Small molecule generic submissions
• GMP documentation systems

Location & Salary

Job Location

Ahmedabad, Gujarat

The walk-in interviews will be conducted at the Pharmazone Ahmedabad office.

Estimated Salary Range

Based on current pharmaceutical industry compensation trends:

• QA Manager/Executive Roles: ₹8 LPA to ₹16 LPA
• QC Professionals: ₹7 LPA to ₹14 LPA
• Regulatory Affairs Professionals: ₹5 LPA to ₹12 LPA
• Project Managers: ₹8 LPA to ₹15 LPA
• Business Development Executive: ₹4 LPA to ₹7 LPA

Salary packages may vary depending on:

• Regulatory market exposure
• GMP compliance expertise
• International filing experience
• Team handling experience
• Technical documentation skills
• Project management expertise

Walk-In Interview Details

Interview Dates & Timings

• 21 May 2026: 06:00 PM to 10:00 PM
• 24 May 2026: 09:30 AM to 12:30 PM

Interview Venue

Pharmazone Ahmedabad Office

Candidates are advised to reach the venue on time with updated resumes and relevant documents.

Application Process

Interested candidates should register by sending their updated CV to:

hr@pharmazones.com

Application Instructions

Candidates should mention:

• Department applied for
• Current designation
• Regulatory market exposure
• Notice period
• Current CTC
• Experience in USFDA/MHRA/EU-GMP environments

Candidates attending the walk-in should carry:

• Updated resume
• Educational certificates
• Experience letters
• Salary documents
• Government ID proof

Why Professionals Prefer Regulatory Affairs Careers?

Regulatory Affairs and GMP consulting are among the fastest-growing career segments in the pharmaceutical industry. Professionals with expertise in regulatory submissions, quality systems, compliance audits, and pharmaceutical documentation are increasingly in demand across global pharmaceutical markets.

Key advantages of these careers include:

• International regulatory exposure
• High-growth pharmaceutical sector opportunities
• Strong long-term career stability
• Better compensation growth
• Opportunities in global compliance operations
• Exposure to USFDA and EU pharmaceutical systems

Pharmazone’s hiring drive offers strong opportunities for professionals planning long-term careers in pharmaceutical compliance and global regulatory operations.

FAQs

1. Which company is conducting the pharma walk-in drive?

Pharmazone is conducting the recruitment drive in Ahmedabad.

2. Which departments have openings?

Openings are available in GMP, Quality Assurance, Quality Control, Regulatory Affairs, Project Management, and Business Development.

3. What experience is required for Regulatory Affairs roles?

Candidates with 2 to 5 years of experience in US or EU regulatory markets can apply.

4. Is USFDA plant experience mandatory?

Yes. Several roles specifically require exposure to USFDA, MHRA, and EU-GMP-approved pharmaceutical plants.

5. What educational qualifications are accepted?

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

6. How can candidates register for the interview?

Candidates can send their updated resumes to hr@pharmazones.com.

Summary Table

Company	Pharmazone
Department Vacancies	QA, QC, Regulatory Affairs, Project Management, Business Development
Qualification	B.Pharm, M.Pharm, B.Sc, M.Sc
Experience	2 to 10 Years
Location	Ahmedabad, Gujarat