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Officer - Quality Control (Chemical)
Dubai, United Arab Emirates · Full Time
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- Experience
- 2–5 yrs
- Salary
- —
- Openings
- 1
- Posted
- 1 week ago
- Work mode
- In office
- Education
- Bachelor's degree in Chemistry or Pharmaceutical Sciences
- Resume
- Required to apply
Where you'll work
Job description
Position Overview
The Officer - QC (Chemical) role is based in Dubai Industrial City within a new pharmaceutical manufacturing establishment. Reporting to the Executive - QC, this position plays a vital role in performing routine chemical and physical tests on raw materials, in-process samples, and finished products to ensure quality and regulatory compliance.
Responsibilities
- Conduct chemical and physical testing of raw materials, intermediates, and finished products following standard test procedures and pharmacopoeial standards.
- Operate and maintain analytical instruments including HPLC, UV-Vis spectrophotometer, FTIR, and dissolution apparatus.
- Maintain accurate and thorough documentation of test outcomes, adhering to Good Documentation Practices (GDP).
- Ensure sampling and testing activities are carried out promptly to align with production timelines and release schedules.
- Assist in the preparation and standardization of reagents, solutions, and volumetric measurements.
- Keep the laboratory environment clean and compliant with Good Laboratory Practices (GLP).
- Report any deviations, out-of-specification results, or non-conformities to the Executive - QC.
- Contribute to method validation and transfer processes when required.
- Adhere to current Good Manufacturing Practices (cGMP) and safety protocols during laboratory operations.
- Engage in internal audits, training activities, and continuous improvement initiatives.
Candidate Profile
- Possess a Bachelor's degree in Chemistry or Pharmaceutical Sciences.
- Have 2 to 5 years of experience in a chemical quality control role within pharmaceutical or chemical industries.
Key Skills and Competencies
- Good foundational knowledge of chemical analysis and instrumental methods such as HPLC, UV, and IR spectroscopy.
- Understanding of pharmacopoeial standards including IP, BP, USP, and EP, along with cGMP guidelines.
- Proficient in handling laboratory glassware and analytical equipment.
- Strong attention to detail and keen observational skills.
- Commitment to maintaining quality and regulatory compliance.
- Ability to collaborate effectively within a team environment.
- Efficient time management and organizational abilities.
- Motivation to learn and adapt within a dynamic manufacturing setup.