Unison Pharmaceuticals Hiring PMT & Regulatory Affairs Professionals

Unison Pharmaceuticals Hiring PMT & Regulatory Affairs Professionals in Ahmedabad

Are you looking for an exciting career opportunity in the pharmaceutical industry? Unison Pharmaceuticals Pvt. Ltd. is expanding its team and is on the lookout for talented professionals in Product Management (PMT) and Regulatory Affairs. Based in Ahmedabad

Vacancies Available at Unison Pharmaceuticals

1. Group Product Manager – PMT (Cardio-Diabetic Division)

Location: Vastrapur, Ahmedabad
Experience Required: Minimum 8+ years in Pharma Product Management/Marketing (PMT)
Division: Cardio-Diabetic

Key Responsibilities:

• Developing and executing product marketing strategies.
• Managing the entire product lifecycle, from concept to launch.
• Coordinating with sales and regulatory teams to ensure product compliance.
• Driving brand awareness and market penetration.

Qualifications:

• B. Pharm/M. Pharm/MBA with at least 8+ years of experience in Pharma PMT.
• Strong knowledge of the cardio-diabetic market.
• Proven track record in product management and marketing strategies.

2. Regulatory Affairs Professional (EU Market – Post-Approval)

Location: Vastrapur, Ahmedabad
Experience Required: 4-6 years in post-approval regulatory affairs, focusing on the EU market

If you have a background in Regulatory Affairs and are experienced in handling post-approval processes for EU-regulated markets, this position is ideal for you. Unison Pharmaceuticals is seeking professionals with a minimum of 4 years of experience in post-approval variation filing and regulatory compliance for pharmaceutical products in Europe.

Key Responsibilities:

• Managing post-approval regulatory submissions, including variation filings for the EU market.
• Ensuring compliance with EU regulatory requirements for pharmaceutical products.
• Coordinating with cross-functional teams to maintain product compliance.
• Preparing and submitting documents to regulatory agencies.

Qualifications:

• B. Pharm/M. Pharm/M.Sc. in life sciences with 4-6 years of experience in regulatory affairs, specifically for the EU market.
• Expertise in post-approval processes, including variation filings.
• In-depth knowledge of EU regulations and guidelines.

How to Apply

If you meet the qualifications, Interested candidates can send their updated CVs to maitrivakil@unisonpharmaceuticals.com. Make sure to mention the position you are applying for in the subject line.