Job Description
Job DescriptionJob Title: QC Chemist I
Location: Central Islip, NY (Onsite)
Job Type: Full-Time | Permanent
Shift: 8:30 AM – 5:00 PM (may vary)
Industry: Pharmaceutical
Experience Required: 2 to 15 years
Compensation: *,000 – *,000
Visa Sponsorship: Not available
Remote Option: No
Job Overview:
We are looking for a dedicated Quality Control Chemist to join our team and perform analytical testing in a GMP-regulated laboratory environment. The ideal candidate will have experience in pharmaceutical product testing and familiarity with various analytical instruments and techniques.
Responsibilities:
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Perform standard and advanced laboratory testing on raw materials, in-process samples, and finished products.
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Operate lab instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.
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Ensure compliance with cGMP, data integrity, and good documentation practices.
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Support deviation investigations, change control activities, and CAPAs.
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Participate in method validations and support production and quality operations.
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Maintain accurate and timely documentation in line with regulatory standards.
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Execute assigned tasks with attention to detail and in alignment with department protocols.
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Collaborate with team members and other departments to meet project deadlines.
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Perform other duties as assigned by management.
Required Qualifications:
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Bachelor’s degree in Chemistry or a related scientific field.
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2–15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector.
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Strong understanding of lab testing and instrumentation.
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Must be able to read, write, and understand scientific materials in English.
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Proficiency with MS Office and laboratory software systems.
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Comfortable working on-site full-time; no remote options.
Preferred Experience:
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Hands-on experience with Inhalation dosage forms (MDI) is a strong advantage.
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Background in testing tablets, capsules, liquids, and solids also acceptable.
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Prior exposure to GMP, FDA regulatory guidelines, and quality systems.
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Experience conducting investigations or root cause analyses.
Work Environment & Physical Requirements:
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Work in a controlled laboratory or production area wearing PPE (lab coat, gloves, goggles, etc.).
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Ability to lift up to 10 kg and stand or walk for extended periods during an 8-hour shift.
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Comfortable using computers and working at a screen for prolonged periods.
Additional Information:
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Must be willing to work weekday shifts and occasional weekends depending on business needs.
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Must be open to working in a pharmaceutical manufacturing environment.
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No employment sponsorship or visa support available.