Regulatory Affairs Associate I

3 days ago


Bengaluru Karnataka, India AstraZeneca Full time

**Job Title: Regulatory Affairs Associate I**

**Career Level - C**

**Introduction to Role**:
**Accountabilities**:
As a Regulatory Affairs Associate, you will be responsible for document management, including uploading and tracking regulatory files and systems according to established AZ procedures and regulatory requirements. You will maintain documentation & records management in Veeva RIM system in accordance with defined standards & process. You will also be responsible for planning, preparing and executing simple submissions, and assisting with the preparation and planning of regulatory dispatches. Additionally, you will be the interface with Health Authority (HA) and its systems for designated regulatory tasks.

**Essential Skills/Experience**:

- Relevant qualification and/or experience in science
- Regulatory experience from biopharmaceutical industry, or other relevant experience
- Some regulatory/medical/technical experience
- Knowledge of AZ business and processes
- Knowledge of AZ submissions, compilation, publishing and approval processes, standards, systems and tools
- Good written and verbal communication skills
- Experience of working with people from locations outside of India, especially from International Regions
- Good commercial and product awareness
- Good Communication and influencing skills
- Good IT/IS skills
- Project planning and organisational skills - Focus on delivery and results
- Flexibility and adaptability
- Interpersonal and networking skills
- Independent and Team working
- Proactivity
- Problem solving

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, we are committed to turning our drug development strategies into reality. We work at all stages of development to translate our life-changing science into medicines to get the best results for AstraZeneca, patients in need and healthcare professionals. We are a diverse and open-minded team harnessing our different skills and experiences. Our differences enable us to explore new ideas and ways of doing things. It keeps us on our toes and excited for what's next. We are striving for technology adoption and automation to drive efficiencies and new innovations.



  • Bangalore, Karnataka, India Anrgi Tech Full time

    Job Title Regulatory Affairs Associate - Authoring Role detailed classification Regulatory Affairs Authoring Job Summary We are seeking highly skilled and experienced Life Sciences LS Regulatory Affairs RA Associate - Authoring to join our LS Practice team The successful candidate will be responsible for LS Regulatory Authoring and or other assigned RA...


  • Bengaluru, Karnataka, India Planet Science Full time

    **About Us**: An established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform **- CLYZO** **Position - Regulatory Affairs Associate.** An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having...


  • Bengaluru, India ANRGI TECH Pvt. Ltd. Full time

    Job Description Job Title: Regulatory Affairs Associate – Authoring.  Role detailed classification Regulatory Affairs Authoring Job Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring...


  • Bengaluru, India ANRGI TECH Pvt. Ltd. Full time

    Job Title: Regulatory Affairs Associate – Authoring.  Role detailed classification Regulatory Affairs Authoring Job Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring and/or other...


  • Bengaluru, India Parexel Full time

    **_Regulatory Affairs Associate _**: **Experience: RIM**: **Relevant experience in Regulatory and should be willing to work in EU Shifts (12:00 - 9.00 PM)**: - **Experience of handling RIM tools - Veeva Vault specifically.**: - **Basic Regulatory knowledge on regulations and Health Authorities.**: - **Excellent communication skills.** **Knowledge and...

  • Regulatory Affairs

    2 days ago


    Bengaluru, Karnataka, India UST Full time

    Role DescriptionJob Title: Regulatory Affairs Associate – Authoring.Role detailed classificationRegulatory Affairs AuthoringJob Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring...

  • Senior Associate

    6 days ago


    Bengaluru, India ClinChoice Full time

    Job Description Job Title: Senior Associate Regulatory Affairs Employment Type: Full time Location: Bengaluru/Hyderabad, India About ClinChoice ClinChoice partners with many of the world's leading pharmaceutical, medical device, and consumer care innovators. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs,...


  • Hyderabad, Telangana Bangalore, Karnataka, India UST Full time

    Job Title Regulatory Affairs Associate - Regulatory Information Management RIM - UST Band B1 Role detailed classification RIM Regulatory Information Management Job Summary We are seeking highly skilled and experienced Life Sciences LS Regulatory Affairs RA Associate - RIM to join our LS Practice team The successful candidate will be responsible for LS...


  • Bengaluru, Karnataka, India Novo Nordisk Full time

    Regulatory Professional I **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN- .- **Department**:RA CMC Diabetes & Obesity**About the department** - RA CMC & Device Bangalore is an integral part of RA CMC & Device and comprised of +60 experienced professionals associated with key regulatory processes covering Chemistry...


  • Bengaluru, India Teva Pharmaceuticals Full time

    Work location: Bangalore & MumbaiRole summary:The Associate II, Complex Gx, Regulatory Affairs is responsible for the preparation and submission of high-quality regulatory filings—both pre- and post-approval—for U.S. FDA-regulated inhalation, implant, ophthalmic, and drug-device combination complex generic products. With moderate to minimal guidance, the...