Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for cGMP operations. Various techniques are utilized in Quality Control including FT-IR, UV, KF, HPLC and GC. Additional functions include daily calibration, stability testing, assay transfers etc. in the Quality Control laboratory.
location: Ridgefield, New Jersey
job type: Contract
salary: $23 - 35 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- The QC Analyst is responsible for performing routine to complex techniques
associated with daily QC release and provides an investigative or technological
orientation in implementing, executing, and interpreting quality procedures and
test methods.
- Perform UV-Vis spectrophotometry, HPLC and Gel assays for in-process and final
product samples.
- Perform pH, karl Fischer, Osmolarity, Rheology analysis in accordance with
approved procedure.
- Perform maintenance on complex laboratory equipment including HPLC and GC
systems.
- Investigate and troubleshoot Quality Control methods.
- Prepare investigations related to 00S/00T results.
- Review QC Data for compliance to procedures and specifications.
- Prepare statistical analysis of results.
- Identify deviations from QC methods.
- Recommend method improvements.
- Work effectively with others to achieve shared goals.
- Interact with external personnel on technical matters requiring coordination
between sites.
- Work independently with minimal supervision and direction.
- Work in compliance with cGMPs.
qualifications:
Basic Qualifications
- Bachelor's Degree in Life Sciences discipline and 2 years' experience in cGMP lab environment, or a
- Master's Degree in Life Sciences discipline and 1 years' experience in cGMP lab environment.
- Proficient in Outlook and Microsoft Word and Excel and lab-based data management systems
- Scientific technical writing ability.
- Experience with pH, KF, FT-IR, GC, HPLC, Gel, UV Vis Spectroscopy and wet chemistry.
- Experience with Empower software.
- Knowledge of lab-based data management systems.
- Familiarity with USP and global compendia requirements.
- Scientific technical writing ability.
skills: Chemistry, High Pressure Liquid Chromatography (HPLC), UV-Vis Spectroscopy, FTIR Spectroscopy, Karl Fischer (KF) Titration, Gel Electrophoresis (SDS-PAGE), Good Manufacturing Practices (GMP), Quality Control (QC)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
