Instagram
youtube
Facebook

Senior Associate (Sterile Exp-Eu Market)

4+ years
Not Disclosed
10 July 24, 2025
Job Description
Job Type: Remote Education: Master’s degree in Pharmacy 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

 

Senior Associate (Sterile Exp – EU Market) – Syneos Health | Gurgaon (Homebased)

Job Summary

Syneos Health is seeking an experienced Senior Associate – Sterile Regulatory Affairs (EU Market) with expertise in post-approval variations, CMC dossiers, and regulatory submissions for sterile drug products. This homebased role is ideal for candidates with 4+ years of experience in EU pharmaceutical regulatory processes, sterile manufacturing, and compliance with global regulatory standards.

Compensation: Not specified (competitive package offered).


Responsibilities

  • Manage regulatory submissions for sterile drug products, including aseptic and terminal sterilization.

  • Review Module 2 and 3 documentation on sterile manufacturing, microbial control, and container closure systems.

  • Handle post-approval changes related to sterile facilities, cleanroom classification, sterilization methods, and equipment upgrades.

  • Prepare and submit components of IND, NDA, and lifecycle maintenance applications.

  • Conduct quality control reviews, ensure high-quality documentation, and maintain regulatory databases.

  • Attend client meetings, build relationships, and support project deliverables.

  • Mentor and review the work of Regulatory Associates or junior team members.

  • Identify risks to project delivery and provide effective issue resolution proposals.

  • Maintain individual training records and ensure compliance with SOPs and global regulatory standards.


Required Skills & Qualifications

  • Master’s degree in Pharmacy (preferred) or Science/Healthcare field.

  • 4+ years of experience in post-approval variations for sterile products (EU market experience is mandatory).

  • Strong knowledge of sterile manufacturing, microbial controls, and CMC documentation.

  • Proficiency in Microsoft Office tools and regulatory databases.

  • Excellent interpersonal, communication, and analytical skills.

  • Ability to work independently and manage multiple projects with tight timelines.

  • Fluent in spoken and written English.


Perks & Benefits

  • Homebased work flexibility with global project exposure.

  • Opportunity to work with leading EU and global regulatory authorities.

  • Career growth through technical training and mentoring.

  • Inclusive Total Self culture supporting diversity and work-life balance.

  • Competitive performance-based rewards.


Company Description

Syneos Health® is a leading biopharmaceutical solutions organization with 29,000 employees across 110 countries. The company partners with global pharma and biotech organizations to provide regulatory, clinical, and commercial solutions, accelerating the delivery of life-saving therapies.


Work Mode: Homebased (Remote) | Location: Gurgaon, Haryana, India
Compensation Range: Not specified


Call-to-Action

Looking to advance your regulatory career in the sterile and EU pharmaceutical domain? Apply now to join Syneos Health and make an impact in global healthcare.