Aneta Pharma Walk In for Regulatory Affairs – Executive, AM Positions

Aneta Pharmaceuticals, a WHO-GMP certified pharmaceutical manufacturing company, is conducting a walk-in interview in Ahmedabad for experienced professionals in Regulatory Affairs. This is a fantastic opportunity for qualified candidates with a B.Pharm or M.Pharm degree and 6 to 12 years of hands-on experience in regulatory submissions across ROW, EU, and CIS markets. If you are looking to advance your career in a dynamic, quality-driven organization, Aneta Pharma welcomes your application.

About Aneta Pharmaceuticals

Incorporated in 2023, Aneta Pharmaceuticals is a growing force in the pharmaceutical manufacturing industry. With a WHO-GMP certified plant, a GLP-compliant Quality Control facility, and a commitment to innovation and integrity, Aneta delivers high-quality healthcare solutions that meet global standards. The company believes in fostering creativity, maintaining unwavering quality, and offering employees a platform to grow professionally.

Job Details: Regulatory Affairs – Executive / Assistant Manager

Job Role: Executive / Assistant Manager – Regulatory Affairs

Experience Required: 6–12 years

Qualification: B.Pharm / M.Pharm

Industry: Pharmaceuticals (Formulations & APIs)

Location: Ahmedabad, Gujarat

Department: Regulatory Affairs

Walk-In Mode: Direct application or contact via email/WhatsApp

Key Responsibilities

As part of Aneta Pharma’s Regulatory Affairs team, your responsibilities will include:

• Preparing, compiling, and reviewing regulatory dossiers for submission in ROW, EU, and CIS markets.
• Ensuring timely product registration submissions in accordance with regional regulatory standards.
• Coordinating with cross-functional teams (QA, QC, R&D, Production) for documentation and technical support.
• Managing communications with regulatory bodies, partners, and internal stakeholders for query resolutions and compliance updates.
• Supporting lifecycle management activities including renewals and variations.
• Maintaining accurate and audit-ready regulatory documentation and databases.
• Monitoring changes in international regulatory guidelines and advising management on compliance strategies.

Candidate Profile & Key Skills

Ideal candidates should demonstrate:

• A strong command of regulatory submission requirements for global markets.
• Proven experience working with dossiers for both formulated pharmaceutical products and APIs.
• Strong problem-solving, communication, and coordination skills.
• Ability to work proactively in cross-functional settings and with regulatory bodies.
• Leadership qualities with experience in mentoring or managing junior regulatory team members.

Walk-In Interview Details & Application Process

Interested and eligible candidates can attend the walk-in or share their updated resume via email or WhatsApp.

Email: hr@anetapharma.com

Mobile/WhatsApp: +91 75758 09274