Senior QA Expert ESO

Reposted 5 Hours Ago
Be an Early Applicant
2 Locations
In-Office
Senior level
Biotech • Pharmaceutical
The Role
The Senior QA Expert ESO ensures compliance with GMP standards, manages quality issues with suppliers, and drives continuous improvement initiatives in pharmaceutical manufacturing.
Summary Generated by Built In

Job Description Summary

#LI-Hybrid
Primary Location: Warsaw, Poland
Other Locations: Mumbai, India; Hyderabad, India
Relocation Support: This role is based in Warsaw, Poland. Novartis is unable to offer relocation support: please only apply if accessible.
Join Novartis in shaping the future of quality excellence!
As a Senior QA Expert ESO, you’ll ensure that all Novartis products manufactured by external suppliers meet international GMP standards and regulatory requirements. Acting as the Single Point of Contact, you’ll drive compliance, foster strong partnerships, and lead continuous improvement initiatives that make a real impact on patient safety and global quality standards.


 

Job Description

Key Responsibilities

  • Act as Single Point of Contact for all quality-related activities at assigned external suppliers.
  • Provide quality input and presence in technical meetings with external suppliers.
  • Ensure supplier qualification and maintain valid Quality Agreements aligned with business needs.
  • Monitor quality trends and drive continuous improvement through KPIs and performance assessments.
  • Ensure site readiness for regulatory inspections and support during audits.
  • Manage quality issues, including complaints, deviations, and out-of-specification results, ensuring timely resolution.
  • Oversee change controls from initiation through implementation and closure.
  • Support manufacturing process and analytical method transfers with robust QA oversight.

Essential Requirements

  • Bachelor’s degree or higher in Pharmacy, Biochemistry/Biotechnology, Chemistry, Microbiology, or a related science.
  • Fluent in English, both spoken and written (minimum C1 level or equivalent certification).
  • Minimum 8 years of experience in the pharmaceutical industry, including 5 years in sterile manufacturing.
  • Expert knowledge of aseptic processes and biologics manufacturing; strong understanding of cGMP for EU and US markets.
  • Advanced experience with FDA, EMA, and other Health Authorities; skilled in risk management and project management.
  • Strong communication and negotiation skills; advanced decision-making abilities and basic leadership experience.

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Benefits and rewards:

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:

https://www.novartis.com/careers/benefits-rewards


 

Skills Desired

Top Skills

Aseptic Processes
Gmp Standards
Qa Oversight
Quality Agreements
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The Company
HQ: Basel
110,000 Employees
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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