Job Description
About the Role
We are seeking a motivated and detail-oriented QC Analyst to join our laboratory team. You will conduct high-quality analytical testing to support production, ensuring compliance with GMP and EHS standards.
You will work with a range of analytical techniques and instruments, including particle size analysis, HPLC, FTIR, Raman, DSC, microscopy, and more. The role involves testing, method development, data review, and reporting, as well as maintaining laboratory compliance and safety standards.
Key Responsibilities
* Perform routine and specialized analytical testing on in-process and composite samples.
* Prepare and review analytical reports, certificates of analysis, and validation documentation.
* Maintain lab cleanliness and adhere to all GMP and EHS procedures.
* Identify and escalate deviations, CAPAs, or changes under supervision.
* Use laboratory IT systems, including Oracle, Trackwise, ComplianceWire, and Minitab.
* Communicate effectively with colleagues, management, and clients.
* Stay up-to-date with industry developments related to particle size analysis and cleaning validation.
Who We’re Looking For
* Science graduate or higher with laboratory experience in a cGxP environment, or extensive industry experience.
* Knowledge of GMP and EHS principles.
* Strong attention to detail, accurate documentation, and time management skills.
* Self-motivated with a professional and positive attitude.
* Ability to work independently or as part of a team.
Shift Pattern: 3-week rotation
* Early Shift: 6:00am – 2:00pm (Mon-Fri)
* Late Shift: 1:30pm – 10:00pm (Mon-Thu), 1:30pm – 7:00pm (Fri)
* Night Shift: 9:00pm – 7:00am
Why Join Us
* Work in a supportive, professional lab environment.
* Opportunity to gain hands-on experience with a wide range of analytical techniques.
* Be part of a team committed to quality, safety, and continuous improvement.