LC-MS Quality Control Research Associate Job in Raritan, New Jersey US
LC-MS Quality Control Research Associate
Every day, Kelly Scientific Resources helps scientific professionals with their careers. Kelly is currently staffing for a Bioanalytical Quality Control Research Associate . This position is taking place at a well-known biotech company in Raritan, NJ. By working with Kelly in this role, you would be eligible for: - A competitive hourly pay rate with weekly checks - Access to newly expanded Medical Plan options - Online continuing education via the Kelly Learning Center - Several employee discounts - And more! This is a 12 month temporary position at 40 hours per week. Job Description : This company develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine. The Research Associate/Quality Control position in the Bioanalytical Department within Global Drug Safety Sciences is a newly established function as a strategic movement to further enhance the quality delivery and compliance. This position will work with other leaders in the department to ensure high quality data from validation and implementation of analytical methods using liquid chromatography and mass spectrometry LC/MS-MS for quantification of new molecular entities in biological matrices. The individual will review the raw data and reports prepared by the other associates. This position will also apply metrics and trend analysis to provide the department leadership team to monitor the quality of the data and reports. This position will also conduct department training on GLP and quality control system and assist on SOP preparation. This position allows the individual to further develop quality control skills in the bioanalytical area and familiarity with current guidance relevant to bioanalytical by interacting with Quality Assurance. The position will be supervised, and on the job training will be offered in the bioanalytical area, with ongoing training in different areas focusing on identifying and recommending solutions to routine problems. Qualifications A minimum of a BA/BS in Biology, Chemistry, Biochemistry, and/or Analytical Chemistry is required. 2 to 4 years of industrial and/or academic laboratory experience is preferred. GLP Bioanalytical LC-MS experience is required. Previous working experience as Quality Control is preferred. Knowledge of a variety of basic scientific techniques and experience working in an analytical laboratory environment is preferred. The preferred candidate is self-motivated, well-organized, productive and has excellent computer and scientific problem solving skills. Ability to work independently and work as part of a team is required. Excellent verbal and written communication skills are required. Familiarity with Good Laboratory Practices GLPs and other regulatory requirements is essential. A strong desire to learn the drug development process is required. For immediate consideration, click the "Apply Now! button, or refer a friend by clicking the "E-mail this job" link provided. Kelly Services, Inc. is an Equal Opportunity Employer. Kelly Services connects professionals with opportunities to advance. As the local offices of Kelly Services do not represent the above position, please apply on-line for immediate consideration. For questions regarding this position, please email or phone 4117@kellyservices.com or 732-246-1396.