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:

• Bachelors 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!

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