Regulatory Affairs Associate I – Teva Pharma Hiring

Regulatory Affairs Associate I – Teva Pharma Hiring, Navi Mumbai

Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals, Navi Mumbai. B.Pharm/M.Pharm/Life Sciences graduates with 2–3 years experience preferred.

Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, is seeking a Regulatory Affairs Associate I for its Navi Mumbai facility. This full-time role offers an exciting opportunity to contribute to global regulatory publishing activities, ensuring timely, accurate, and compliant submissions for EU, US, and Canadian markets. If you are a pharmacy or life sciences graduate with regulatory publishing experience, this role could be your gateway to a rewarding career in regulatory affairs.

Company Overview

Teva Pharmaceuticals is on a mission to make good health more affordable and accessible. Operating in nearly 60 countries, Teva supplies medicines to 200 million people worldwide every day. The company is a proud producer of many products listed on the World Health Organization’s Essential Medicines List. With a rich heritage in generics, innovative specialty medicines, and biosimilars, Teva combines global expertise with local insights to improve healthcare worldwide.

Joining Teva means being part of a diverse team, committed to delivering excellence, innovation, and patient access to essential therapies.

Job Role & Responsibilities

As a Regulatory Affairs Associate I – RA, you will:

• Responsible for executing GRO Regulatory Data Analytics operations in line with Work Instructions and SOPs. Primarily will be Regulatory Data Analytics Service related to product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows).
• Operationally hands-on in terms of carrying out data management activities as an individual contributor. This will require a thorough understanding of the structure and contents of a regulatory dossier (i.e. will be fluent in navigating and understanding the contents of a dossier). Registration data management will require a thorough understanding of the registration data structures, workflows, and applicable work instructions etc.
• Perform Quality Control (QC) and data integrity checking, as part of the Regulatory Data Analytics operation, to confirm the accuracy and completeness of the Teva Global Registration database.
• Represent GRO Regulatory Data Analytics across the wider Global Regulatory Affairs community. Must be proficient at building effective working relationships with all stakeholder and customer groups.
• Responsible for providing effective business project contributions for projects focused on improving regulatory data quality, the provisioning of regulatory data for internal re-use via system integration, or the implementation of any business or technology change that impacts regulatory data or the regulatory technology landscape.

Eligibility / Qualifications

Education:

• Masters in Pharmacy or Masters in Science/Life Sciences
• College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts.

Experience:

• Required: Bachelor’s or Master’s degree in Life Sciences or Information Technology.
• Preferred: MS in a scientific or information technology discipline

Minimum Years of Work Experience:

• Required: 1–3 years (preferably with experience in regulatory operations/affairs).

Location & Salary

• Location: Navi Mumbai, Maharashtra, India – 400706
• Work Model: Full-time, onsite
• Compensation: Competitive salary based on experience, with industry-standard benefits
• Reporting To: Manager – Regulatory Submission Management

Application Process

Interested candidates can apply directly via Teva’s official career portal:
Apply Here

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