Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Executive / Sr. Executive Regulatory Affairs

Orion Pharma
orion pharma
5-8 years
Not Disclosed
Hyderabad, Mumbai, India
10 Feb. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Executive / Senior Executive – Regulatory Affairs

Job ID: 1194

Location: Mumbai, Maharashtra, India and Hyderabad, India (Hybrid)

Employment Type: Full-Time

Job Category: Regulatory Affairs | Pharmaceutical Compliance | eCTD Submissions | EU Regulatory Affairs

Experience Required: 5–8 years in international regulatory affairs with confirmed knowledge of EU requirements and ICH guidelines


About the Company

Orion Pharma is a globally operating pharmaceutical company with over a century of expertise in developing, manufacturing, and marketing human and veterinary medicines, active pharmaceutical ingredients, and consumer health products. Orion Pharma fosters a culture of respect, diversity, and innovation, empowering employees to create meaningful impact for patients and society.


Role Overview

The Executive / Senior Executive – Regulatory Affairs will contribute to global regulatory compliance by preparing, reviewing, and managing pharmaceutical registration dossiers, variations, amendments, renewals, and eCTD submissions according to EU regulatory requirements. This role requires collaboration across multiple departments and close monitoring of regulatory updates to ensure timely and accurate filings.

The position offers a hybrid work environment with opportunities to work from office three days a week and remotely for two days, promoting work-life balance while supporting global regulatory operations.


Key Responsibilities

  • Prepare, check, and review pharmaceutical and quality sections of registration dossiers, variations, amendments, annual reports, and renewals as per EU regulations

  • Identify and classify changes according to EU regulatory variation guidance

  • Prepare responses to regulatory deficiency letters following EU requirements

  • Collaborate with cross-functional teams and external partners to ensure regulatory compliance

  • Maintain and update internal regulatory systems and documentation

  • Participate in the continuous development of regulatory skills within the team

  • Perform other duties assigned by supervisors to support regulatory operations

  • Achieve deliverables within agreed timelines while ensuring compliance with global regulatory standards


Required Experience & Skills

  • 5–8 years of experience in international regulatory affairs within the pharmaceutical industry

  • Strong knowledge of EU regulatory requirements and ICH guidelines

  • Experience in formulation analytical development, formulation development, pharmaceutical product development, and eCTD submissions is advantageous

  • Fluent in written and spoken English

  • Ability to work independently and collaboratively within a team

  • Task-oriented, with strong learning agility and teamwork skills

  • Proficiency in Microsoft Office and regulatory documentation tools


Educational Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related discipline from a recognized university


Work Environment & Benefits

  • Hybrid work model (3 days office, 2 days remote)

  • Flexible, supportive, and high-spirited workplace culture

  • Opportunities for professional development and regulatory expertise growth

  • Contributing to impactful pharmaceutical projects across oncology, pain, neurological, and respiratory therapies