Urgently Hiring: Staff Chemist, Quality Control

Join a team that's making a tangible difference. We're seeking a Staff Chemist, Quality Control! Experience the best of both worlds with this role based in our innovative Remote office. This position requires a strong and diverse skillset in relevant areas to drive success. In recognition of your expertise, this position offers a salary of a competitive salary.

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What you will do:Â
•  Lead analytical chemistry testing for new product development, existing medical device changes, and lab validation activities.
• Oversee daily lab operations, including preventative maintenance, calibration, purchasing, metrics, and sample organization.
• Execute and validate analyses using GC-FID, GC-MS, ICP-MS, TOC, and other laboratory equipment.
• Manage departmental initiatives, setting timelines, milestones, and aligning policies with industry best practices and regulatory requirements.
• Evaluate test data, approve internal testing documentation, and conduct root cause analyses and equipment troubleshooting.
• Partner with cross-functional teams (RA, AO, Ops) to ensure alignment with business unit project timelines.
• Present lab KPIs and findings to management and cross-functional stakeholders.
• Coach, mentor, and train junior scientists and team members in analytical chemistry and lab best practices.

What are we looking for:Â

Required
• Bachelor of Science in Chemistry, Biochemistry, Chemical Engineering or a similar science degree with 4+ years’ experience in analytical chemistry testing is required.
• Minimum 3 years’ experience in medical device, pharmaceutical, cosmetic or chemical industry.
• Experience leading or writing analytical test method validations for TOC, UV/VIS, HPLC, GC, or ICP instrumentation using ISO, ICH, or USP standards.
• Knowledge of ANSI, AAMI, ISO, ICH, or USP guidelines for residual chemical analysis.
• Minimum 3 years’ experience in using HPLC-MS, HPLC-UV, GC-MS, GC-FID, or ICP-MS.

Preferred
• Master of Science in Chemistry, Biochemistry, Chemical Engineering or a similar science degree.
• Demonstrated ability to manage day-to-day activities within a chemistry lab such as familiarity with calibration schedules, purchasing, sample organization, and lab metrics.
• 2+ years’ experience conducting root cause analysis or out-of-specification investigations.
• Knowledge of cGLP and cGMP processes with experience in following standards such as ISO 17025, USP 1225 or USP 232.
• Experience in LIMS (i.e. Labvantage, ilab) and statistical software (i.e. Minitab). Apply Job!

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Take the Next Step

Are you ready for this challenge? Apply now and let's discuss how you can become a vital part of our success story.

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