Quality Control Analyst II

AllSTEM Connections; City of Rensselaer (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

A recruiting firm is seeking a Quality Control Analyst II in the City of Rensselaer, NY. Candidates must have a Bachelor's degree in Chemistry or a related field and 3-5 years of experience in the pharmaceutical industry. Responsibilities include conducting analytical testing on various products, maintaining QC instruments, and supporting quality data reviews. Ideal candidates would come from a cGMP or GLP environment, ensuring compliance and quality in testing processes.

Qualifications

• Minimum 3-5 years’ experience in pharmaceutical industry environment or equivalent combination of education and experience.
• Experience working in cGMP or GLP pharmaceutical industry environment preferred.

Responsibilities

• Perform analytical testing for incoming, in-process and final products.
• Back up for QC analytical instrument maintenance and calibration.
• Assist in the review of QC data and provide summaries to management as needed.

Skills

Analytical testing

Chromatography (HPLC/GC)

Wet chemistry assays

Laboratory housekeeping

QC data evaluation

Education

Bachelor’s degree in Chemistry or related field

Tools

HPLC

GC

UV/Visible Spectrophotometer

Total Organic Carbon Analyzer

Job description

Need Local Candidate and only US Citizen/GC

Job Title: Quality Control Analyst II

Duration: 6+ Months

Qualifications

• Bachelor’s degree in Chemistry or related field
• Minimum 3-5 years’ experience in pharmaceutical industry environment or equivalent combination of education and experience

Preferred

• Experience working in cGMP or GLP pharmaceutical industry environment

Responsibilities

1. Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc.
2. Perform chromatography (HPLC/GC, UPLC) with minimal qualification and training, wet chemistry assays, analytical chemistry assays, HPLC, GC, IR, UV, etc. and raw material testing and/or sampling
3. Back up for QC analytical instrument maintenance and calibration
4. Perform QC general laboratory equipment maintenance, laboratory housekeeping and preparation of the laboratory for audits
5. Perform or assist with QC method qualifications, transfers and validations
6. Assist with the evaluation of new equipment and processes
7. Assist in the review of QC data and provide summaries to management as needed
8. Assist QC Management, as needed, in the completion of OOS, deviations, and CAPAs investigations for QC
9. Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure