Compass Consulting
Base pay range
$25.00/hr - $27.97/hr
Direct message the job poster from Compass Consulting
Pharmaceutical | Biotech | Quality Assurance | Recruiter Connecting Organizations With Industry Experts
4 days, 10hrs per day: Sunday - Wednesday 1pm to Midnight (swing shift)
Our client focuses on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases.
Responsibilities
Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices.
Execute analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers.
Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness.
Assist with monitoring and the control of laboratory supply and critical reagent inventories.
Qualify as trainer for specified methods, provide training to less experienced staff.
Exhibit proactive communication upon occurrence of compliance risks and deviations from laboratory procedures, perform initiation of investigation records within required timeframes.
Provide input or assay support to the progression of test method validation, investigations, technical studies, and method transfer protocols.
Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization.
Perform other responsibilities, including support for other QC areas, as deemed necessary.
Skills
Experience with quality management systems, current Good Manufacturing Practices, and QC principles.
Demonstrated working knowledge with respect to certified functional activities.
Good documentation, written and verbal communication skills are essential.
Must possess the ability to perform most tasks with minimal supervision.
Computer literacy is required, proficiency with Microsoft Word and Excel is essential; experience with PowerPoint, Access, or Visio is desired.
Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.
Education
Bachelor of Science degree.
0-3 years of relevant laboratory experience; QC specific experience is preferred.
Seniority level
Entry level
Employment type
Contract
Job function
Quality Assurance and Analyst
Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr
Direct message the job poster from Compass Consulting
Pharmaceutical | Biotech | Quality Assurance | Recruiter Connecting Organizations With Industry Experts
4 days, 10hrs per day: Sunday - Wednesday 1pm to Midnight (swing shift)
Our client focuses on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases.
Responsibilities
Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices.
Execute analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers.
Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness.
Assist with monitoring and the control of laboratory supply and critical reagent inventories.
Qualify as trainer for specified methods, provide training to less experienced staff.
Exhibit proactive communication upon occurrence of compliance risks and deviations from laboratory procedures, perform initiation of investigation records within required timeframes.
Provide input or assay support to the progression of test method validation, investigations, technical studies, and method transfer protocols.
Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization.
Perform other responsibilities, including support for other QC areas, as deemed necessary.
Skills
Experience with quality management systems, current Good Manufacturing Practices, and QC principles.
Demonstrated working knowledge with respect to certified functional activities.
Good documentation, written and verbal communication skills are essential.
Must possess the ability to perform most tasks with minimal supervision.
Computer literacy is required, proficiency with Microsoft Word and Excel is essential; experience with PowerPoint, Access, or Visio is desired.
Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.
Education
Bachelor of Science degree.
0-3 years of relevant laboratory experience; QC specific experience is preferred.
Seniority level
Entry level
Employment type
Contract
Job function
Quality Assurance and Analyst
Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr