Looking to advance your pharmaceutical career in the UAE? Adcan Pharma, a leading pharmaceutical manufacturing company in Abu Dhabi, is hiring an ADL Officer with expertise in API analysis, raw material testing, and analytical method validation. Apply today and grow with an industry leader.
Contents
- 1 Join a Reputed Pharmaceutical Manufacturer in the UAE
- 2 Why Choose Adcan Pharma?
- 3 Position: Analytical Development Laboratory (ADL) Officer
- 4 Key Responsibilities
- 5 Educational and Professional Qualifications
- 6 Required Experience
- 7 Preferred Technical Skills
- 8 Career Benefits at Adcan Pharma
- 9 High-Income Career in Pharmaceutical Quality Control
- 10 How to Apply
- 11 Application Email
- 12 Useful Pharmaceutical Resources
- 13 Keywords to Boost Your Career & Visibility
- 14 Final Note
Join a Reputed Pharmaceutical Manufacturer in the UAE
Located in ICAD III, Abu Dhabi, Adcan Pharma is committed to delivering high-quality medicines that meet global regulatory standards. As part of our expanding team, you’ll play a key role in analytical testing and method validation within our state-of-the-art Analytical Development Laboratory.
Why Choose Adcan Pharma?
Adcan Pharma offers excellent opportunities for career advancement and professional growth. You’ll gain exposure to international regulatory frameworks, advanced pharmaceutical instrumentation, and modern quality control systems while working with a talented and passionate team in a high-tech environment.
Position: Analytical Development Laboratory (ADL) Officer
We are currently looking for a highly experienced ADL Officer who can independently perform analytical method development, method validation, and API testing. The ideal candidate should be detail-oriented, experienced in handling GMP documentation, and capable of working in a fast-paced regulated lab environment.
Key Responsibilities
- Conduct comprehensive analytical testing of APIs, excipients, and raw materials
- Perform method validation as per ICH guidelines and regulatory expectations
- Operate instruments such as HPLC, GC, FTIR, UV-Vis, and dissolution testers
- Review Drug Master Files (DMFs) and technical documents
- Interpret results based on pharmacopeial standards (USP, BP, EP)
- Document investigations for OOT, OOS, deviations, DCRs, and CCFs
- Support analytical method transfer and ensure lab compliance with GMP and GLP
Educational and Professional Qualifications
Candidates must hold a Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. A strong understanding of analytical method validation, regulatory guidelines, and quality control principles is essential for this role.
Required Experience
A minimum of 7 years’ hands-on experience in pharmaceutical analytical development is required. Candidates should have in-depth knowledge of analytical techniques, instrument calibration, and be able to handle regulatory audits confidently. Prior work in a GMP-compliant lab is highly preferred.
Preferred Technical Skills
- Proficiency in wet chemistry, instrumental analysis, and analytical troubleshooting
- Experience in method development and validation of APIs and raw materials
- Ability to manage lab information management systems (LIMS)
- Understanding of ICH Q2(R1) and other regulatory frameworks
- Familiarity with regulatory audit preparation and compliance management
Career Benefits at Adcan Pharma
By joining Adcan Pharma, you’ll benefit from a competitive salary, UAE labor law benefits, and opportunities for ongoing learning. You will also be part of a company that values integrity, innovation, and international pharmaceutical standards.
High-Income Career in Pharmaceutical Quality Control
This role offers a high-paying job in pharmaceutical quality control and development in the UAE, ideal for professionals seeking long-term international careers. Skills in HPLC, analytical method validation, and API testing are in high demand across the global pharmaceutical industry.
How to Apply
To apply for this exciting position, send your updated CV to careers@adcanpharma.ae. Ensure your resume includes details of your analytical experience, instruments handled, and knowledge of GMP compliance.
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Application Email
careers@adcanpharma.ae
Mention “Application for ADL Officer – API & Raw Material Analysis” in the subject line.
Useful Pharmaceutical Resources
Explore essential regulatory guidance to prepare for this role:
- ICH Q2(R2) Guidelines on Validation of Analytical Procedures
- US FDA GMP Guidelines
- USP Pharmacopeia Reference
Keywords to Boost Your Career & Visibility
- High-paying jobs in pharmaceutical industry
- Analytical development officer jobs in Abu Dhabi
- HPLC and API testing job openings UAE
- Pharmaceutical quality control careers UAE
- GMP and GLP jobs in pharmaceutical labs
- ICH guidelines-based analytical testing jobs
- Pharmaceutical method validation jobs 2025
Final Note
If you are a dedicated analytical chemist or pharmaceutical scientist seeking a career in regulatory-compliant pharma manufacturing, this opportunity is perfect for you. Don’t miss your chance to become a key part of Adcan Pharma’s quality development team.