We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst with a strong background in analytical chemistry and hands-on experience in the medical device or pharmaceutical industry. The ideal candidate will hold a degree in Chemistry (PhD preferred) and possess at least two years of experience in a regulated QC laboratory environment, including proficiency in High-Performance Liquid Chromatography (HPLC).
Key Responsibilities
* Perform routine and non-routine testing of raw materials, in-process samples, and finished products using HPLC and other analytical techniques.
* Ensure all laboratory activities comply with GMP, ISO, and relevant regulatory standards.
* Maintain and calibrate laboratory instruments, ensuring optimal performance and documentation.
* Interpret and report analytical data accurately, identifying trends and deviations.
* Support method development, validation, and troubleshooting of analytical procedures.
* Collaborate with cross-functional teams including R&D, production, and regulatory affairs.
* Participate in investigations, CAPAs, and continuous improvement initiatives.
* Maintain meticulous records and contribute to audit readiness.
Qualifications & Experience
* Degree in Chemistry (PhD preferred; MSc or BSc acceptable with strong experience).
* Minimum 2 years of experience in a Quality Control Laboratory within the medical device or pharmaceutical industry.
* Proven expertise in HPLC operation, troubleshooting, and data interpretation.
* Familiarity with GMP, ISO 13485, and regulatory compliance.
* Strong analytical thinking, attention to detail, and problem-solving skills.
* Excellent communication and documentation abilities.
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