Analytical QA Jobs – Ferring Pharmaceuticals, a global leader in reproductive medicine, maternal health, gastroenterology, and urology therapeutics, is actively hiring an Executive / Sr. Executive – Analytical QA for its quality assurance function.
This senior role requires 7–9 years of hands-on experience in raw data review, chromatographic/spectroscopic data integrity, method validation, transfer protocols, instrument qualification, 21 CFR Part 11 compliance, stability program oversight, and CGLP laboratory compliance — ideal for immediate joiners with strong analytical QA expertise in regulated pharmaceutical environments.
Contents
About the Company
Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical company headquartered in Switzerland with a long-standing commitment to improving lives through innovative hormone and peptide-based therapies.
The company has a strong global presence and operates multiple manufacturing and R&D sites adhering to stringent international regulatory standards (including USFDA, EMA, and ICH guidelines).
Ferring is recognized for its focus on patient-centric innovation, scientific excellence, ethical practices, and a supportive work culture that values quality, integrity, and professional growth.
Job Details
- Company Name: Ferring Pharmaceuticals
- Position: Executive / Sr. Executive – Analytical QA
- Experience: Minimum 7–9 Years (immediate joiners preferred)
- Qualification: B.Pharm / M.Pharm / M.Sc
- Location: Not explicitly mentioned (likely Mumbai / Navi Mumbai or major Ferring site in India; confirm during application)
- Work Type: On-site (laboratory and quality oversight role)
Job Description
The Executive / Sr. Executive – Analytical QA will play a critical role in ensuring data integrity, analytical compliance, and regulatory readiness in the QC laboratory.
The position demands deep expertise in reviewing raw data, identifying hidden data integrity issues, ensuring proper integration practices, and maintaining full compliance with ICH, 21 CFR Part 11, and CGLP standards.
Executive / Sr. Executive – Analytical QA
- Department: Analytical Quality Assurance
- Market: Pharmaceuticals – Regulated Formulations
- Role: Executive / Sr. Executive – Analytical QA
- Experience: 7–9 Years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc
Skills/Qualifications
- Strong experience in raw data review (chromatograms, spectra, worksheets) and identification of hidden data integrity issues
- Expertise in reviewing analytical reports (assay, dissolution, impurities, stability)
- Proficiency in proper integration practices for HPLC, GC, and other chromatographic systems
- Hands-on knowledge of method validation protocols/reports and method transfer documentation
- Thorough understanding of IQ/OQ/PQ of instruments and 21 CFR Part 11 software qualification
- Experience in stability program QA, protocol adherence, and laboratory compliance oversight
- Familiarity with ICH Q2 (validation) and ICH Q14 (analytical procedure development)
- Strong documentation, audit readiness, and CGLP compliance skills
- Immediate joining ability preferred
Key Responsibilities
- Review raw data (chromatograms, spectra, worksheets) for accuracy and integrity
- Scrutinize analytical reports including assay, dissolution, impurities, and stability data
- Identify and flag hidden data integrity issues, outliers, atypical results, reprocessing/re-dilution concerns
- Ensure proper integration practices and audit trail compliance for HPLC/GC systems
- Review and approve method validation protocols/reports and method transfer documents
- Oversee IQ/OQ/PQ of analytical instruments and 21 CFR Part 11 software qualification
- Monitor stability program adherence, calibration/PM records, and logbook compliance
- Perform routine laboratory QA checks and ensure overall CGLP compliance
- Support audit preparation and respond to internal/external audit findings
Benefits/Perks
- Career growth in a global specialty biopharmaceutical leader
- Exposure to advanced analytical QA and data integrity practices
- Opportunities for skill enhancement in regulatory compliance and method lifecycle
- Competitive compensation and performance-based rewards
- Supportive, inclusive work culture focused on quality and patient impact
How to Apply
Send your updated resume highlighting 7–9 years of analytical QA experience (raw data review, method validation, 21 CFR Part 11, stability oversight, CGLP compliance) to: saiprasanna.kesari@ferring.com
Mandatory — Mention in subject line: Exe/Sr.Exe – AQA For more analytical QA jobs, regulatory compliance roles, pharma QA openings, and careers in India, visit Pharma Recruiter.
Apply immediately—Ferring prefers candidates ready to join quickly!
Why You Should Join
Ferring Pharmaceuticals offers a purpose-driven, high-compliance environment ideal for senior QA professionals passionate about data integrity, analytical excellence, and regulatory standards.
With a global focus on reproductive health, gastroenterology, and urology, the company provides meaningful work, exposure to advanced analytical systems, career advancement, and the opportunity to contribute to innovative therapies that improve patients’ lives.
Joining Ferring means working in a values-led organization that balances scientific rigor with empathy and long-term impact.
FAQs
What is the minimum experience required for the Analytical QA role at Ferring?
7–9 years of strong hands-on experience in raw data review, method validation, stability oversight, and 21 CFR Part 11/CGLP compliance.
Is immediate joining mandatory?
Preferred—candidates who can join quickly will be prioritized.
Where is the job located?
Likely Navi Mumbai / Mumbai area (Ferring’s major India site); exact location to be confirmed during application.
How do I apply and what should I include?
Email your CV to saiprasanna.kesari@ferring.com with subject line Exe/Sr.Exe – AQA; clearly highlight relevant experience in analytical QA and data integrity.
