What are the responsibilities and job description for the Laboratory Technician III position at Careers Integrated Resources Inc?
Title: Senior QC Analyst
Location: Ridgefield, NJ
Duration: 12 Months Possible Extension
Shift: 1st ( 8-4:30 EST, Mon-Fri )
Manager Notes:
Description:
The Senior 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, GC and Gel assays for in-process and final product samples.
Perform UV-Vis spectrophotometry, HPLC and Gel assays for in-process and final product samples.
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.
Participate in training of less experienced staff on new procedures.
Transfer methods from support groups to the QC laboratory.
Develop and author complex and explicit documentation for new and current procedures and technical reports.
Provide technical leadership and guidance for the successful completion of major laboratory projects.
Implement new quality control procedures.
Transfer and develop new methods.
Identify deviations from QC methods.
Recommend method improvements.
Implement and monitor personnel training.
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.
Practice safe work habits and adhere to Client's safety procedures and guidelines
Basic Qualifications
Bachelor's Degree in Life Sciences discipline and 4 years’ experience in cGMP lab environment, or a
Master's Degree in Life Sciences discipline and 2 years’ experience in cGMP lab environment.
Proficient in Outlook and Microsoft Word and Excel and lab-based data management systems
Scientific technical writing ability.
HPLC (high pressure liquid chromatography) experience.
Preferred Qualifications
Experience with Agilent 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
Location: Ridgefield, NJ
Duration: 12 Months Possible Extension
Shift: 1st ( 8-4:30 EST, Mon-Fri )
Manager Notes:
- Bachelor's Degree in Life Sciences discipline and 4 years’ experience in cGMP lab environment
- Master's Degree in Life Sciences discipline and 2 years’ experience in cGMP lab environment.
- HPLC (high pressure liquid chromatography) experience.
- Perform UV-Vis spectrophotometry, HPLC, GC and Gel assays for in-process and final product samples.
Description:
The Senior 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, GC and Gel assays for in-process and final product samples.
Perform UV-Vis spectrophotometry, HPLC and Gel assays for in-process and final product samples.
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.
Participate in training of less experienced staff on new procedures.
Transfer methods from support groups to the QC laboratory.
Develop and author complex and explicit documentation for new and current procedures and technical reports.
Provide technical leadership and guidance for the successful completion of major laboratory projects.
Implement new quality control procedures.
Transfer and develop new methods.
Identify deviations from QC methods.
Recommend method improvements.
Implement and monitor personnel training.
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.
Practice safe work habits and adhere to Client's safety procedures and guidelines
Basic Qualifications
Bachelor's Degree in Life Sciences discipline and 4 years’ experience in cGMP lab environment, or a
Master's Degree in Life Sciences discipline and 2 years’ experience in cGMP lab environment.
Proficient in Outlook and Microsoft Word and Excel and lab-based data management systems
Scientific technical writing ability.
HPLC (high pressure liquid chromatography) experience.
Preferred Qualifications
Experience with Agilent 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
