QC Chemist I

Job Title: Quality Control (QC) Chemist

Location: Central Islip, NY

Employment Type: Full-Time, Exempt Professional

Work Hours: General Shift – 8:30 AM to 5:00 PM (May vary depending on business needs)

Position Overview:

The QC Chemist is an individual contributor role responsible for performing sample testing and analysis using various techniques and equipment within the Quality Control laboratory. The role may be modified based on department needs and the individual's experience, education, and skills.

Key Responsibilities:

Conduct routine and advanced testing or analysis in a designated testing group or department.

Perform specialized testing as required, operating specialized equipment.

Test raw materials and ensure release processes are followed.

Operate and manage laboratory equipment such as Karl Fischer, HPLC, GC, ICP, and other specialized instruments.

Lead investigation activities related to non-conformances and laboratory issues.

Ensure compliance with data integrity and cGMP practices and procedures.

Maintain documentation practices in accordance with regulatory requirements.

Perform any other duties as assigned by the Quality Control Department or Section Head.

Education & Experience Requirements:

Bachelor's degree (BS or BA) in Chemistry, Pharmaceutical Sciences, or a related field (Required)

Experience: 2–15 years in a Quality Control role within the pharmaceutical industry

Technical Skills:

Working knowledge of instruments such as Karl Fischer, HPLC, GC, ICP, and Particle Size analysis

Experience in Inhalation products (MDI) is a plus

Familiarity with data integrity, good documentation practices, and cGMP standards

Language: Proficient in reading, writing, and communicating scientific work in English

Preferred Skills & Experience:

Experience in Pharma (Not Bio Pharma)

Strong organizational and problem-solving skills, including the ability to analyze complex data sets

Ability to work well both independently and in a team environment

Physical Requirements & Work Conditions:

Ability to stand or walk unassisted for 75% or greater of an 8-hour shift.

Ability to lift up to 10 kg without assistance.

Must be able to wear appropriate personal protective equipment (PPE) at all times when required.

Work in a cGMP laboratory or manufacturing environment.

May be required to work weekends or holidays depending on business needs.

Additional Requirements:

Must be willing to work in a pharmaceutical setting and follow all cGMP guidelines.

Must be flexible with shift schedules as required by business needs (first or second shift).

No remote work is available.

No employment sponsorship or work visas available for this position.