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시간

Officer - Quality Control (Chemical)

Himalaya Wellness Europe

Dubai, United Arab Emirates · 정규직

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경험
2~5세
샐러리
채용 공고
1
게시됨
2주 전
작업 모드
사무실에서
교육
Bachelor's degree in Chemistry or Pharmaceutical Sciences
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직무 설명

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.

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