Job Description
Astrix is proud to partner with a globally recognized contract research, development, and manufacturing organization (CDMO) serving the pharmaceutical and biotech industries. We are seeking a motivated and detail-oriented Quality Control (QC) Chemist to join the team.
If you're passionate about laboratory science, quality assurance, and contributing to life-saving innovations, this is your chance to work in a high-impact environment with room to grow.
Pay: 35-44/hr.
Schedule: 6pm-6am, Monday-Friday
Key Responsibilities:
- Perform analytical testing on raw materials, in-process and final products, and stability samples using balances, pipettes, pH meters, UV/Vis spectrophotometers, TOC analyzers, and more.
- Conduct chromatography (HPLC, GC) testing following comprehensive training and qualification.
- Execute wet chemistry assays and routine water sample collections.
- Maintain and calibrate QC analytical instruments and general lab equipment.
- Support QC laboratory housekeeping and audit readiness efforts.
- Assist in reviewing QC data and summarizing findings for management.
- Participate in deviation investigations, CAPAs, and out-of-specification (OOS) documentation under guidance from QC Management.
- Serve as backup for sample receipt, shipment, result distribution, and external lab coordination.
Qualifications:
Required:
- Bachelor’s degree in Chemistry or a related scientific field.
- 3 years of experience in a pharmaceutical QC Chemist or analytical laboratory role.
Preferred:
- Experience working in a cGMP, GLP, or FDA-regulated environment.
Key Competencies & Skills:
- Strong understanding of analytical chemistry principles and lab techniques.
- Excellent written and verbal communication skills.
- Ability to manage time effectively and work independently in a fast-paced environment.
- Proficiency with Microsoft Office and laboratory data systems.
- Working knowledge of FDA regulations (21 CFR 211, 820, 600) and ISO standards (9001, 13485) is a plus.
- Familiarity with statistical analysis, report writing, and documentation best practices.
Physical Requirements:
- Must be able to sit, stand, walk, kneel, or crouch for extended periods.
- Ability to lift up to 50 lbs as needed.
- Requires fine motor skills, visual focus, and manual dexterity for laboratory work.
Why Join Us?
- Be part of a company with a national and global impact in pharmaceutical development.
- Gain valuable experience in an FDA-regulated environment with career advancement opportunities.
- Work alongside a collaborative team that values innovation, quality, and continuous learning.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!