WhatsApp Group Join Now
Telegram Group Join Now

Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026

Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026 in Navi Mumbai. Pharma professionals with regulatory, QA, or production experience

If you are looking to grow your career in regulatory affairs with a globally recognized pharmaceutical company, Teva Pharmaceuticals has opened an exciting opportunity in India. The company is currently hiring a Regulatory Affairs Associate I in Navi Mumbai. This role is ideal for professionals with experience in regulatory documentation, quality systems, or pharmaceutical manufacturing who want exposure to global submission processes.

Below is a detailed overview of the opportunity rewritten exclusively for IndiaPharmaJobs.in readers. Regulatory Affairs Associate I Job


Company Overview

Teva Pharmaceuticals is one of the world’s leading manufacturers of generic medicines and specialty pharmaceuticals. With a presence in multiple countries, the organization is known for delivering cost-effective healthcare solutions and expanding access to essential medicines globally. The company operates across diverse therapeutic areas and plays a significant role in supplying affordable medications worldwide.

Working at Teva offers professionals exposure to international regulatory environments, collaborative global teams, and opportunities for long-term career growth within the pharmaceutical industry. Regulatory Affairs Associate I Job


Job Location & Employment Type

  • Location: Navi Mumbai, Maharashtra, India
  • Job Role: Regulatory Affairs Associate I
  • Employment Type: Full-time
  • Industry: Pharmaceutical / Regulatory Affairs

This role is based at Teva’s Navi Mumbai operations and involves working with regulatory documentation related to global submissions.


Department Details

The opening is within the Regulatory Affairs Department, which supports submission management, compliance documentation, and lifecycle maintenance of regulatory filings. The position focuses on maintaining regulatory documentation, assisting with submission preparation, and supporting regulatory compliance activities aligned with international standards.

Related Jobs  Sun Pharma Hiring for Executive FRD Non Oral

Key Roles & Responsibilities

Selected candidates will be responsible for supporting regulatory submissions and documentation processes under guidance from senior team members. Major responsibilities include: Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026

  • Assisting in preparation of annual reports and regulatory supplements for submissions.
  • Supporting amendments and documentation updates aligned with regulatory requirements.
  • Reviewing technical documents linked to change controls, including batch records and specifications.
  • Ensuring regulatory data accuracy within internal databases and trackers.
  • Maintaining compliance of approved filings with relevant global regulations.
  • Learning regulatory filing classifications and submission requirements through practical exposure.
  • Coordinating with internal departments such as Quality, Production, and Documentation teams.
  • Supporting additional regulatory projects as assigned by management.

This role is suitable for candidates looking to build expertise in regulatory lifecycle management and global filing standards. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026


Eligibility Criteria

Education

  • M.Pharm in Regulatory Affairs or Quality Assurance preferred
  • Candidates with relevant pharma backgrounds may also be considered

Experience

  • Minimum 2 years of experience in:
    • Regulatory Affairs
    • Quality Control or Quality Assurance
    • Pharmaceutical R&D or analytical labs
    • Production environments within pharma/biotech industry

Experience in regulated markets or submission support will be an added advantage.


Skills Required

Candidates should possess a combination of technical and soft skills, including:

  • Basic understanding of regulatory documentation workflows
  • Familiarity with submission requirements and compliance systems
  • Proficiency in MS Word, Excel, and digital documentation tools
  • Strong attention to detail and documentation accuracy
  • Good written and verbal communication skills
  • Ability to multitask and manage shifting priorities
  • Team collaboration along with independent task handling
  • Organizational skills for managing regulatory trackers
Related Jobs  Freshers Jobs Business Executive Jobs in Bangalore at Merck

Candidates with exposure to USFDA-related processes will stand out during the selection process. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026


Salary & Benefits

  • Compensation will be as per company norms
  • Additional benefits may include:
    • Corporate work environment
    • Exposure to global regulatory practices
    • Career advancement opportunities
    • Learning and development support

Exact salary details are typically discussed during the recruitment process.


Selection Process

The recruitment process may include multiple evaluation stages such as:

  1. Online application screening
  2. HR shortlisting
  3. Technical or functional interview
  4. Final discussion and offer release

Candidates with relevant regulatory experience and strong documentation skills are more likely to progress.


How to Apply

  • Application Mode: Online application via the official Teva careers portal
  • Interested candidates should apply through the company’s official career page.

Applicants already employed at Teva are advised to use the internal career system for priority consideration. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026

Apply Here


Important Dates

  • Application closing dates are not specified, so early application is recommended.

Why Apply for This Pharma Job?

Here are some strong reasons to consider applying for this opportunity:

  • Work with a globally established pharmaceutical organization
  • Gain hands-on experience in international regulatory submissions
  • Build a strong foundation in regulatory lifecycle management
  • Opportunity to transition into senior regulatory roles in future
  • Exposure to regulated market documentation and compliance frameworks
  • Ideal stepping stone for professionals targeting global pharma careers

For regulatory professionals aiming to move beyond routine QA or production roles, this job offers valuable domain exposure. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026

Related Jobs  Internship Jobs in Baddi at Venus Remedies

Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform that shares verified pharmaceutical career opportunities. We are not affiliated with Teva Pharmaceuticals or any hiring organization. Candidates are advised to apply only through official company channels and verify all job details independently before applying. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026


Final Words

If you have experience in regulatory affairs, quality, or pharmaceutical documentation and want to work with a globally recognized pharma company, this opportunity at Teva is worth considering. With international exposure and long-term growth potential, this role can significantly strengthen your regulatory career profile. Apply early to maximize your chances of selection. Regulatory Affairs Associate I Job at Teva Pharma Apply Online Pharma Jobs 2026


WhatsApp Group Join Now
Telegram Group Join Now

Leave a Comment

Join WhatsApp
Join Telegram
Telegram
DMCA.com Protection Status
Submit Resume βœ•
Make Resume βœ•