Manager - Regulatory Affairs

4 weeks ago


Delhi India Tata Play Ltd Full time

Job Description

ROLE SUMMARY

Ensure Regulatory compliances and handle Government Affairs

KEY DUTIES AND RESPONSIBILITIES

1. Legal expertise in Media & Entertainment industry. We prefer a person with experience in Broadcasting sector or who has worked with a Law firm handling Broadcasting issues.
2. Interact and be a bridge between Tata Play and TRAI, MIB, DoT, Industry bodies
3. Conversant with issues to meet and explain company's position to various Regulatory Authorities- MIB, TRAI, DoT, WPC, NOCC and others
4. Responding to correspondences and queries from and to Regulatory Authorities MIB, TRAI, WPC, NOCC and others
5. Ensuring timely and regulatory consistent response to MIB/TRAI Customer complaints and monitoring and managing the quality levels of the LPO handling these complaints
6. Researching and providing inputs on the various sectoral consultation papers issued by TRAI.
7. Interacting with relevant cross-function teams to obtain inputs for the response.
8. Manage workflow for consumer related grievances
9. Collaborate with several internal /external stakeholders and rapidly respond to all consumer grievances received
10. Analysis of regulatory data submitted to statutory authorities
11. Pro-active management of various statutory timelines and corresponding actions
12. Keen interest in identifying systemic/ procedural inefficiencies and working with cross-function teams for the process change.
13. Identify process out-sourcing opportunities and thereafter interact with relevant internal teams for operationalizing the same

TECHNICAL COMPETENCIES

- Good understanding of Media & Entertainment laws, Information Technology laws
- Government & External Liaising
- Ability to meet strict time-sensitive deadlines
- Proficient with Microsoft words and excel
- Excellent written and verbal communications and interpersonal skills
- Managing heavy workflow independently
- Good law firm experience

EDUCATION

B.A. LLB. with 6 yrs plus experience



  • Delhi, India Wembrace Biopharma Private Limited Full time

    Job Description Job Profile The Regulatory Affairs Manager (RAM) for Africa, MENA, and LATAM will lead regulatory strategy, submissions, approvals, and life-cycle management of pharmaceutical, biotech, and nutraceutical products across these diverse regions. The role requires a strong understanding of local health authority requirements, WHO guidance, and...


  • New Delhi, India Self-employed Full time

    Company DescriptionFounded in the commercial operations year of , NextGen Pharma, a majority-owned subsidiary of Ormendes SA, Switzerland, has emerged as a leading provider of specialized botanical and nutraceutical solutions. With a focus on proprietary Targeted Bacterio-Therapy (TBT), our offerings cater to diverse therapeutic segments ranging from...


  • New Delhi, India Self-employed Full time

    Company Description Founded in the commercial operations year of , NextGen Pharma, a majority-owned subsidiary of Ormendes SA, Switzerland, has emerged as a leading provider of specialized botanical and nutraceutical solutions. With a focus on proprietary Targeted Bacterio-Therapy (TBT), our offerings cater to diverse therapeutic segments ranging from...


  • New Delhi, India Self-employed Full time

    Company Description Founded in the commercial operations year of , NextGen Pharma, a majority-owned subsidiary of Ormendes SA, Switzerland, has emerged as a leading provider of specialized botanical and nutraceutical solutions. With a focus on proprietary Targeted Bacterio-Therapy (TBT), our offerings cater to diverse therapeutic segments ranging from...


  • Delhi, Delhi, India Ace Cathtech Pvt. Ltd. Full time ₹ 6,00,000 - ₹ 9,00,000 per year

    Company DescriptionAce Cathtech Pvt Ltd, established in April 2024, is a cutting-edge manufacturer of premium medical devices, specializing in Nephrology Products, Cardiac Surgery Equipment, Critical Care, and Anesthesia Products. Located in Faridabad, Haryana, our state-of-the-art facility adheres to the highest manufacturing standards, including a Class 7...


  • New Delhi, Delhi, India, Delhi Panacea Biotec Full time

    Position: Sr. Manager / AGM – Regulatory AffairsQualification: M.Sc. / Ph.D. (Life Sciences, Biotechnology, or related discipline) Experience: 13–16 years in Regulatory Affairs (vaccines/biologicals)Role:The role is responsible for global product registrations (LatAm, Africa, GCC etc.), WHO Prequalification, Product lifecycle management, and regulatory...


  • New Delhi, India Panacea Biotec Full time

    Position: Sr. Manager / AGM – Regulatory Affairs Qualification: M.Sc. / Ph.D. (Life Sciences, Biotechnology, or related discipline)Experience: 13–16 years in Regulatory Affairs (vaccines/biologicals)Role:The role is responsible for global product registrations (LatAm, Africa, GCC etc.), WHO Prequalification, Product lifecycle management, and...


  • New Delhi, India Panacea Biotec Full time

    Position: Sr. Manager / AGM – Regulatory Affairs Qualification: M. Sc. / Ph. D. (Life Sciences, Biotechnology, or related discipline) Experience: 13–16 years in Regulatory Affairs (vaccines/biologicals) Role: The role is responsible for global product registrations (Lat Am, Africa, GCC etc.), WHO Prequalification, Product lifecycle...


  • New Delhi, India Panacea Biotec Full time

    Position: Sr. Manager / AGM – Regulatory Affairs Qualification: M.Sc. / Ph.D. (Life Sciences, Biotechnology, or related discipline) Experience: 13–16 years in Regulatory Affairs (vaccines/biologicals) Role: The role is responsible for global product registrations (LatAm, Africa, GCC etc.), WHO Prequalification, Product lifecycle management, and...


  • Delhi, Delhi, India Panacea Biotec Full time ₹ 12,00,000 - ₹ 36,00,000 per year

    Position:Sr. Manager / AGM – Regulatory AffairsQualification:M.Sc. / Ph.D. (Life Sciences, Biotechnology, or related discipline)Experience:13–16 years in Regulatory Affairs (vaccines/biologicals)Role:The role is responsible for global product registrations (LatAm, Africa, GCC etc.), WHO Prequalification, Product lifecycle management, and regulatory...