QC Raw Material Analyst (10 months Contract)
Position overview: The QC Raw Material Analyst is responsible for sampling, testing, and releasing incoming raw materials in accordance with GMP, pharmacopeial standards, and company procedures.
Ensures materials meet specifications to safeguard product quality and patient safety.
Responsibilities
Perform testing and analysis of raw materials, in-process, and final products, as well as environmental samples, following SOPs, Test Methods, and cGMP standards.
Document, review, and ensure data integrity and compliance with GMP requirements.
Support laboratory operations, including equipment maintenance, housekeeping, inventory control, and preparation of standards and reagents.
Manage sample logistics, such as retention storage, external lab coordination, document control, and sample shipments.
Participate in method transfers, validations, and equipment qualification activities.
Troubleshoot analytical methods, equipment issues, and support OOS or deviation investigations.
Contribute to continuous improvement and operational efficiency initiatives as assigned by the Manager.
Qualifications
Degree in Chemistry or Biological Chemistry.
Relevant work experience preferably with Raw Material handling.
Understanding and execution of compendial monographs and the chemistry fundamentals behind methods.
Experience with UV, Infrared Spectroscopy, Osmolality, HPLC, pH, Conductivity, Polarimetry, Refractometry, Density meters, Titration (manual and automatic), and compendial testing listed in USP, JP, and EP monographs.
Why join us?
Generous Leave Policy.
Comprehensive Health & Wellness Coverage: medical and dental coverage.
Shape the Future: make a difference in the pharmaceutical industry while advancing your career.
How to Apply
Please submit your resume outlining your qualifications and experience relevant to the role.
Additional Details
Seniority level: Entry level
Employment type: Contract
Job function: Quality Assurance
Industries: Pharmaceutical Manufacturing
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