Quality Control Chemist

Elvis Eckardt Recruitment; New York (NY); On-site; USD 65,000 - 90,000; Full time

Job summary

A leading recruitment agency is seeking a Quality Control Chemist for a prominent pharmaceutical company located in Central Islip, NY. The ideal candidate will have a solid background in Quality Control testing, particularly within a cGMP-regulated environment. Responsibilities include conducting in-process testing and ensuring adherence to quality standards. Qualified applicants will hold a Bachelor's degree in Chemistry and possess strong analytical skills, attention to detail, and English proficiency.

Benefits

Relocation support up to USD 6,000 for eligible candidates

Qualifications

• Minimum 2 years experience in QC role, preferably in pharmaceuticals.
• Experience with inhalation products is beneficial.
• Familiarity with cGMP documentation is a plus.

Responsibilities

• Conduct in-process testing according to batch record instructions.
• Perform routine and advanced testing of materials and products.
• Ensure compliance with data integrity and documentation practices.

Skills

Analytical skills

Attention to detail

Knowledge of testing techniques

Strong English proficiency

Education

Bachelor’s degree in Chemistry or Physical Science

Tools

Karl Fisher

HPLC

GC

ICP

Job description

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Elvis Eckardt Recruitment provided pay range

This range is provided by Elvis Eckardt Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$65,000.00/yr - $90,000.00/yr

Direct message the job poster from Elvis Eckardt Recruitment

Entrepreneur & Founder | Robin Hood meets Recruitment | Fractional TA Leader | Moonshot | Father to a cheeky | Extended Workbench for the Big 4…

Role: Quality Control Chemist

Location: Central Islip, NY, USA

Industry: Pharmaceuticals/Biotechnology/Clinical Research

Type: Full-Time | Onsite | General Shift: 8:30 AM – 5:00 PM

Experience Required: 2 – 15 years

Visa Status: Only US Citizens and Green Card Holders. No employment sponsorship or visa transfers.

Relocation Support: Up to USD 6,000 provided for eligible candidates.

About The Job:

We are seeking a QC Chemist I with a solid background in pharmaceutical Quality Control testing.

The role is suited for professionals who are detail-oriented, analytically skilled, and experienced in handling a variety of testing techniques within a cGMP-regulated environment.

Key Responsibilities:

• Conduct in-process testing (e.g. weight, thickness, hardness, disintegration, friability) in accordance with manufacturing batch record instructions.
• Perform routine and advanced testing of raw materials and finished products.
• Operate instruments including Karl Fisher, HPLC, GC, Particle size, and ICP.
• Ensure adherence to data integrity and cGMP documentation practices.
• Lead or assist in investigations and lab documentation processes.
• Collaborate with team members to support timely and compliant laboratory operations.

MUST HAVE Qualifications:

• Bachelor’s degree (BS or BA) in Chemistry or a Physical Science discipline.
• Experience in the pharmaceutical industry (strictly no bio-pharma).
• Educational background in Chemistry (BS/BA preferred).
• Working knowledge of Inhalation products (MDI) is a plus (also open to experience with tablets, capsules, liquids, and solids).
• Familiarity with key instruments: Karl Fisher, HPLC, GC, Particle Size Analysis, ICP.
• Strong English proficiency (spoken, written, and reading) for scientific documentation.

Work Conditions:

• Must be comfortable working in a regulated lab with PPE (e.g., lab coats, goggles, masks).
• Ability to stand/walk unaided for long periods and lift up to 10 kg.
• Must be open to shift flexibility and occasional weekend work as required.

Application Process:

To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.

Equal Opportunity Employer:

We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.

Contact: Elvis Eckardt

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Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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