QC Chemist II

Cipla; Town of Islip (NY); On-site; USD 65,000 - 85,000; Full time

Job summary

A leading global pharmaceutical company is seeking a Chemist to perform testing in the QC laboratory. The role involves conducting routine and advanced testing, operating specialized equipment, and ensuring compliance with regulatory standards. Candidates should possess a Bachelor's degree in physical sciences and strong analytical skills. This position requires working in a cGMP environment and may involve flexible shifts.

Qualifications

• Conduct routine and advanced testing in a specific department.
• Experience with scientific software and inhalation products is a plus.

Responsibilities

• Perform testing of samples using various techniques in the QC laboratory.
• Lead investigation activities ensuring compliance with cGMP standards.
• Conduct raw materials testing and release activities.

Skills

Organizational Skills

Analytical Skills

Teamwork

Proficiency in English

Education

Bachelor's degree in physical sciences

Tools

HPLC

GC

Karl Fisher

ICP

Microsoft Office

Job description

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FLSA Classification: Full-Time, Exempt Professional

Work Location: Central Islip, NY (Unit 3)

Work Hours: General Shift: 8:30AM – 5:00PM (may vary based on business needs)

Reports To: Quality Control Manager

Purpose:

The job of the "Chemist" is to perform testing of samples using various techniques or equipment in the QC laboratory. The specific duties may vary depending on the department, group, or testing focus, and will be tailored based on the individual’s education, training, and experience.

Scope:

This description outlines the general nature, responsibilities, and expectations of the Chemist role. It is not exhaustive but provides a framework of the skills and knowledge required. The role may be adjusted according to department needs and individual qualifications.

Duties and Responsibilities:

• Conduct routine and advanced testing in a specific department or group.
• Operate specialized equipment such as Karl Fisher, HPLC, GC, Particle size analyzers, ICP.
• Lead investigation activities and ensure data integrity and compliance with cGMP and documentation standards.
• Perform raw materials testing and release activities.
• Other duties as assigned by the Department Head or Section Supervisor.

Education and Experience:

• Bachelor's degree in physical sciences (BS or BA).
• Proficiency in English, both written and spoken.
• Strong organizational, analytical, and teamwork skills.
• Experience with scientific software and Microsoft Office.
• Experience with Inhalation products (MDI) is a plus.

Working Conditions:

Work is performed in a cGMP laboratory or manufacturing environment requiring personal protective equipment. Work may involve solvents, powders, and other materials typical of pharmaceutical settings. Shifts may include day, evening, night, weekends, or holidays.

Physical Requirements:

• Stand or walk for most of an 8-hour shift; lift up to 10 kg as needed.
• Wear PPE as required; work at a computer for extended periods.

Professional and Behavioral Competencies:

• Willingness to work in pharmaceutical packaging settings and flexible shifts.
• No remote work; no sponsorship or work visas.

About the Company:

Cipla is a leading global pharmaceutical company committed to high-quality medicines. We value our employees as our greatest assets and aim to make healthcare accessible worldwide.

InvaGen Pharmaceuticals, a Cipla subsidiary, specializes in generic medicines across various therapeutic areas.

EEO Statement:

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, disability, or veteran status.

Nearest Major Market: Long Island
Nearest Secondary Market: New York City