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Executive - Analytical

Orion Pharma
orion pharma
3-6 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 – Analytical Affairs

Job ID: 1104

Location: Mumbai, Maharashtra, India / Hyderabad, Telangana, India (Hybrid)

Company: Orion Pharma

Employment Type: Full-Time

Job Category: Analytical Affairs | Regulatory Affairs | Stability Studies | Quality Documentation

Experience Required: 3–6 years of experience in analytical development, stability studies, and regulatory documentation within pharmaceutical industry


About the Company

Orion Pharma is a globally operating Nordic pharmaceutical company with over a century of experience in building well-being. With more than 4,000 employees worldwide, Orion develops, manufactures, and markets human and veterinary pharmaceuticals as well as active pharmaceutical ingredients (APIs).

The company’s portfolio includes proprietary and generic medicines and consumer health products. Core R&D therapy areas include oncology, pain management, respiratory disorders, and neurological diseases. Orion operates as a responsible employer with a strong focus on innovation, regulatory excellence, and global quality standards.


Role Overview

The Executive – Analytical Affairs will be responsible for planning and coordinating stability studies, reviewing analytical documentation, supporting regulatory submissions in CTD format, and managing quality documentation for externally manufactured products.

This hybrid role requires strong expertise in analytical method validation, method transfer, stability data evaluation, Product Quality Review (PQR) preparation, and coordination with Contract Research Organizations (CROs). As there are no in-house laboratories in India, the role involves extensive collaboration with external partners and global stakeholders.


Key Responsibilities

  • Plan stability studies and prepare or review stability protocols and reports

  • Prepare technical documentation in CTD format for regulatory submissions

  • Coordinate and follow up stability studies with Contract Research Organizations (CROs) and Chemical Quality Control (CQC) laboratories

  • Manage and track analytical method validation and method transfer activities at CROs

  • Write, review, and approve analytical and pharmaceutical documents including validation reports, variation documents, and regulatory query responses

  • Evaluate and review analytical methods and validation documentation prepared by CROs

  • Review and comment on change controls, deviations, temperature excursions, stability data, and process validation documents for externally supplied products

  • Author and manage analytical methods and documentation within internal IT systems

  • Prepare Product Quality Reviews (PQRs) for in-house production products and ensure timely approval

  • Review externally supplied PQRs and coordinate with vendors and stakeholders for clarifications

  • Request, track, and follow up PQR-related data

  • Perform theoretical evaluation of physico-chemical properties of drug products and raw materials

  • Provide analytical and regulatory support for local in-licensing activities

  • Collaborate with cross-functional teams and support the broader Indian Pharmaceutical team

  • Undertake additional responsibilities as assigned by supervisors


Required Experience

  • 3–6 years of relevant experience in analytical affairs, quality control, regulatory documentation, or stability management

  • Strong understanding of ICH guidelines, CTD documentation, and global regulatory requirements

  • Experience working with CROs and external laboratories

  • Hands-on exposure to method validation, method transfer, stability data evaluation, and PQR preparation

  • Familiarity with change control, deviation management, and pharmaceutical quality systems

  • Experience handling externally manufactured products preferred


Educational Qualifications

  • Master’s or Bachelor’s degree in Pharmacy, Analytical Chemistry, Pharmaceutical Sciences, or related Life Sciences discipline


Work Model

  • Hybrid working model

  • Locations: Mumbai (Andheri East) and Hyderabad