Saga Hiring Executive RA, BD & PV

BPharm MPharm Executive Vacancies Ahmedabad

BPharm/MPharm Executive RA, BD & PV vacancies (2–5 yrs) at Saga Lifesciences, Ahmedabad, Gujarat. Apply via email.

Saga Lifesciences Ltd. is expanding its professional team and inviting applications from qualified pharmacy graduates for Regulatory Affairs, Business Development, and Pharmacovigilance roles at its Ahmedabad, Gujarat location. With operations across more than 40 countries, the company is strengthening its regulatory and commercial functions to support growing global pharmaceutical markets.

If you are a B.Pharm or M.Pharm graduate with 2 to 5 years of experience and seeking growth in regulatory affairs, international pharmaceutical business development, or drug safety and pharmacovigilance, this opportunity offers direct exposure to EU and semi-regulated markets.

Company Overview

Saga Lifesciences Ltd. is a fast-growing pharmaceutical manufacturer with a strong international footprint spanning over 40 countries. The company operates in regulated, semi-regulated, and ROW (Rest of World) markets, focusing on compliance-driven manufacturing, product registration, and global distribution.

Operating in multiple international territories requires strict adherence to global regulatory guidelines, pharmacovigilance systems, and product lifecycle management practices. Organizations serving EU and international markets must maintain structured documentation, risk management systems, and regulatory submission frameworks.

Professionals joining Saga Lifesciences gain exposure to:

• EU regulatory submission processes
• International product registration strategies
• Pharmacovigilance and drug safety monitoring
• Global pharmaceutical business expansion models
• Dossier preparation and lifecycle management

Global regulatory and safety compliance is a high-value segment within the pharmaceutical industry. Roles in Regulatory Affairs and Pharmacovigilance are considered among the most stable and high-demand pharmaceutical careers due to increasing international oversight.

Job Role & Responsibilities

Saga Lifesciences is hiring for the following positions:

1. Executive – Regulatory Affairs (RA)

Market Focus: EU, Semi-Regulated & ROW Markets
Qualification: B.Pharm, M.Pharm
Experience: 2–5 Years

Key Responsibilities:

• Preparing and reviewing regulatory dossiers for EU and semi-regulated markets
• Coordinating with international regulatory authorities for product approvals
• Handling variations, renewals, and post-approval submissions
• Maintaining regulatory documentation in CTD/eCTD format
• Supporting product registration and lifecycle management
• Monitoring changes in international regulatory guidelines

Candidates must demonstrate understanding of regulatory submission processes, documentation compliance, and pharmaceutical registration systems. Experience with EU regulatory frameworks is highly valuable.

Regulatory Affairs executives directly influence product approval timelines and market access strategies.

2. Executive – Business Development

Qualification: B.Pharm, M.Pharm
Experience: 2–5 Years

Key Responsibilities:

• Identifying new pharmaceutical business opportunities in EU and ROW markets
• Coordinating with international distributors and marketing partners
• Preparing product portfolios and commercial proposals
• Supporting contract negotiations and pricing discussions
• Conducting market research for product expansion strategies

Business Development professionals play a strategic role in expanding pharmaceutical market reach and increasing global revenue streams.

Candidates should have strong communication skills and understanding of pharmaceutical product portfolios and regulatory pathways.

3. Pharmacovigilance Officer

Qualification: B.Pharm, M.Pharm
Experience: 2–5 Years

Key Responsibilities:

• Monitoring adverse drug reactions (ADR) and safety reports
• Preparing Periodic Safety Update Reports (PSUR)
• Maintaining pharmacovigilance databases
• Ensuring compliance with global drug safety regulations
• Supporting signal detection and risk assessment activities
• Coordinating with regulatory bodies for safety reporting

Pharmacovigilance professionals are responsible for drug safety monitoring and regulatory compliance post-marketing. This is a highly specialized field aligned with global regulatory requirements.

Eligibility / Qualifications

Educational Qualifications (comma-separated):

B.Pharm, M.Pharm (Pharmaceutics, Regulatory Affairs, Pharmacology, Pharmaceutical Analysis)

Experience Requirements:

• 2 to 5 years of relevant pharmaceutical industry experience
• Exposure to EU or international markets preferred (for RA & BD roles)
• Pharmacovigilance database handling experience preferred (for PV role)

Required Skills:

• Knowledge of global regulatory guidelines (EU, ROW)
• Strong documentation and compliance discipline
• Communication and coordination abilities
• Understanding of pharmaceutical lifecycle management

Candidates without relevant pharmaceutical exposure may not meet eligibility criteria.

Location & Salary Insights

Location: Ahmedabad, Gujarat

Ahmedabad is a major pharmaceutical manufacturing and export hub in India. The region houses multiple regulatory-compliant facilities and international pharmaceutical operations.

Compensation will depend on:

• Market exposure (EU, semi-regulated markets)
• Technical expertise in RA, PV, or BD functions
• Years of pharmaceutical experience
• Compliance and documentation capability

Regulatory Affairs and Pharmacovigilance roles typically offer strong salary growth due to regulatory complexity and global compliance responsibilities.

Application Process

Interested candidates should send their updated resumes to:

Email: ho.hr@sagalifesciences.com
Contact Number: 8347011179

Application Steps:

1. Update your CV highlighting relevant regulatory, pharmacovigilance, or business development experience.
2. Mention exposure to EU or international markets clearly.
3. Include details of pharmacovigilance database handling (if applicable).
4. Email your application to the HR contact provided.

Shortlisted candidates will be contacted for further interview rounds.

Why These Roles Offer Strong Career Growth

Global pharmaceutical operations require strict regulatory compliance, safety monitoring, and commercial expansion strategies. Professionals working in Regulatory Affairs, Pharmacovigilance, and Business Development gain strategic visibility across product development and international markets.

Key growth advantages include:

• Exposure to EU regulatory frameworks
• Drug safety and pharmacovigilance system training
• International market registration experience
• Cross-functional collaboration with global partners

These roles build long-term career stability and leadership potential in pharmaceutical regulatory management.

Career Progression Opportunities

Candidates selected for these roles may progress toward:

• Regulatory Affairs Manager
• International Business Development Manager
• Pharmacovigilance Manager
• Global Regulatory Strategy Lead
• Drug Safety Compliance Head

Strong international regulatory exposure significantly increases long-term earning potential.

Frequently Asked Questions (FAQs)

1. What qualifications are required?

B.Pharm or M.Pharm is mandatory.

2. Is EU regulatory exposure necessary?

It is preferred for Regulatory Affairs and Business Development roles.

3. Are freshers eligible?

No. Minimum 2 years of experience is required.

4. Which markets does the company serve?

EU, semi-regulated markets, and ROW (Rest of World).

5. How do I apply?

Send your resume to ho.hr@sagalifesciences.com.

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Job Summary

Company	Saga Lifesciences Ltd.
Vacancies	Executive – Regulatory Affairs; Executive – Business Development; Pharmacovigilance Officer
Required Education	B.Pharm, M.Pharm
Experience	2–5 Years