QC Chemist III (3rd Shift) Job at Astrix, Albany, NY

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  • Astrix
  • Albany, NY

Job Description

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!

Job Tags

Contract work, Work at office, Monday to Friday, Night shift,

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