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Quality Control Analyst I

Spectraforce Technologies
United States, New York, Pearl River
Apr 16, 2026
Position Title: Quality Control Analyst I

Work Location: Pearl River, NY, 10965


Assignment Duration: 6 Months



Work Schedule


Monday through Friday, 0900-1700. Weekend work possible


HM Notes:

Open to candidates willing to relocate at own expense

Possibility of extension

Free parking onsite

Fully onsite

MS and PHD degrees considered overqualified

Role will work in a team lab environment

No heaving lifting

Exposure to and will work with Isopropyl alcohol

3+ years of professional experience considered overqualified, this is an entry level role

Must have Skills/ Experience: Bachelor's degree in science degree (Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines)

Previous lab experience in school or professional role

MS Office

Description:

This position supports daily routine activities in the Quality Control laboratory, while adhering to site work instructions and procedures. This position requires the individual to perform routine cGMP activities as scheduled to support laboratory testing and functions.

Activities to be performed by this role include Environmental Monitoring (EM) of laboratory spaces, Bioburden and EM sample incubation, transfer and reads, results documentation and entry into data management system, maintenance of laboratory supplies and inventory, sample receipt, sample inventory and tracking, and cleaning of GMP lab spaces, Biological Safety Cabinets, and controlled temperature units according to current procedures. Additional activities may be assigned as required.

Key Accountabilities

Performs current lab support activities as described by strictly adhering to SOP, SWI, Federal Regulations, cGMP, training modules (when applicable), policies and procedures and safety procedures. Performs laboratory support activities as scheduled by laboratory management to meet the needs of the QC Microbiology Lab.

Completes required paperwork and documentation in a cGMP laboratory as per company procedures.

Assist with maintaining safety and compliance of the laboratory work area; Perform cleaning of laboratories, equipment, and ancillary areas as required; Attend/Contribute to scheduled team meetings, department and safety meetings.

Performs peer review of laboratory documentation.

Performs additional activities related to QC laboratory operations when required.

Basic Qualifications:

4 years' science degree (Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines)

Preferred Skills:

Prior hands-on laboratory experience.
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