Job Description

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

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.

• Perform standard and advanced laboratory testing on raw materials, in-process samples, and finished products.

• Operate lab instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.

• Ensure compliance with cGMP, data integrity, and good documentation practices.

• Support deviation investigations, change control activities, and CAPAs.

• Participate in method validations and support production and quality operations.

• Maintain accurate and timely documentation in line with regulatory standards.

• Execute assigned tasks with attention to detail and in alignment with department protocols.

• Collaborate with team members and other departments to meet project deadlines.

• Perform other duties as assigned by management.

• Bachelor's degree in Chemistry or a related scientific field.

• 2 15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector.

• Strong understanding of lab testing and instrumentation.

• Must be able to read, write, and understand scientific materials in English.

• Proficiency with MS Office and laboratory software systems.

• Comfortable working on-site full-time; no remote options.

• Hands-on experience with Inhalation dosage forms (MDI) is a strong advantage.

• Background in testing tablets, capsules, liquids, and solids also acceptable.

• Prior exposure to GMP, FDA regulatory guidelines, and quality systems.

• Experience conducting investigations or root cause analyses.

• Work in a controlled laboratory or production area wearing PPE (lab coat, gloves, goggles, etc.).

• Ability to lift up to 10 kg and stand or walk for extended periods during an 8-hour shift.

• Comfortable using computers and working at a screen for prolonged periods.

• Must be willing to work weekday shifts and occasional weekends depending on business needs.

• Must be open to working in a pharmaceutical manufacturing environment.

• No employment sponsorship or visa support available.

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