QC Analyst

System One; Orangeburg (NY); On-site; USD 30,000 - 32,000; Part time

Benefits offered by this job

Health benefits

401(k) plan

Dental and vision coverage

Job summary

System One is seeking a QC Analyst in Orangeburg, NY for a contract position. The role involves performing automated and manual tests across Clinical Chemistry, Critical Care, coagulation, and microbiology, following GMP standards.

6:00am to 2:30pm onsite with responsibilities spanning testing, documentation, maintenance, and adherence to SOPs. The ideal candidate has a Bachelor's in Biology, Chemistry, or Medical Technology and 3–6 months of related experience, with strong GMP documentation

Qualifications

• Bachelor's degree in Biology, Chemistry, or Medical Technology.
• 3–6 months of research experience (academic, internship, co-op) or industry experience.
• Ability to perform automated and manual laboratory tests.
• Strong documentation skills in accordance with GMP standards.
• Ability to perform routine maintenance and troubleshooting of lab equipment.

Responsibilities

• Perform analyses of Clinical Chemistry, Critical Care, coagulation, and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements.
• Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs, including raw material, in-process, and finished product testing.
• Interpret test results against specifications and decide if assays pass or fail.
• Maintain documentation of all work performed in accordance with GMP requirements.
• Perform product stability, proficiency, environmental testing, and water system testing.
• Conduct routine preventive maintenance, troubleshooting, cleaning, and calibration of lab equipment.
• Update departmental SOPs and QC Monographs as directed.
• Perform microbial testing per SOPs and QC Monographs.
• Order required laboratory supplies, reagents, and other consumables.
• Monitor proper storage conditions and expiration dates of materials.
• Dispose of hazardous and bio-hazardous materials following proper procedures.
• Maintain retain samples according to established procedures.
• Maintain statistical process control charts and other tracking reports.

Skills

Analytical testing

Documentation skills

GMP knowledge

Education

Bachelor's Degree in Biology, Chemistry, or Medical Technology

Job description

Job Title: QC Analyst

Location: Orangeburg, NY

Type: Contract

Compensation: $22.00 to $23.00

Work Model: Onsite - onsite

Hours: 6:00am to 2:30pm

Responsibilities

• Perform analyses of Clinical Chemistry, Critical Care, coagulation, and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements


• Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs, including raw material, in-process, and finished product testing


• Interpret test results against specifications and decide if assays pass or fail


• Maintain documentation of all work performed in accordance with GMP requirements


• Perform product stability, proficiency, environmental testing, and water system testing


• Conduct routine preventive maintenance, troubleshooting, cleaning, and calibration of lab equipment


• Update departmental SOPs and QC Monographs as directed


• Perform microbial testing per SOPs and QC Monographs


• Order required laboratory supplies, reagents, and other consumables


• Monitor proper storage conditions and expiration dates of materials


• Dispose of hazardous and bio-hazardous materials following proper procedures


• Maintain retain samples according to established procedures


• Maintain statistical process control charts and other tracking reports

Requirements

• Bachelor's Degree in Biology, Chemistry, or Medical Technology


• 3-6 months of research experience (academic, internship, co-op) or industry experience


• Ability to perform automated and manual laboratory tests


• Strong documentation skills in accordance with GMP standards


• Ability to perform routine maintenance and troubleshooting of lab equipment


• Familiarity with SOPs and QC Monographs


• Excellent organizational and monitoring skills for storage conditions and expiration dates


• Knowledge of hazardous waste disposal procedures

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.