Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV hepatitis B hepatitis C and influenza including Harvoni and Sovaldi.
Position: Quality Control Technician I - QC Lab Support
Location: Frederick MD 21704
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift Timings: 7:00am-6:00pm (Sun - Wed)
Job Description:
Responsibilities (include but are not limited to):
-
Receive incoming samples verify documentation and log sample information into LIMS.
-
Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
-
Label store and organize samples according to established procedures and storage requirements.
-
Coordinate sample transfers to internal and external testing labs.
-
Perform routine cleaning maintenance and restocking of sample storage areas.
-
Collaborate with MM QA and other QC functions-including Corporate QC-to support requirements around sampling testing and disposition.
-
Manage and complete all shipping activities within QC functions.
-
Complete routine review of records such as sample chain of custody forms processing logs logbooks and other documentation generated within QC Lab Support.
-
Assist with deviation and investigation activities as needed.
-
Provide updates during daily and weekly meetings.
-
Participate in Lean Lab and other Operational Excellence initiatives.
-
Comply with all safety quality and regulatory guidelines.
-
Perform other duties as assigned.
Basic Qualifications:
-
Bachelors Degree OR
-
AA Degree and 2 years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory OR
-
High School Degree and 3 years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.
Preferred Qualifications:
-
Strong knowledge in applying GMP in QC lab.
-
Exceptional attention to detail and ability to keep track of multiple ongoing projects
-
Proficient in Microsoft Office Excel Visio and other related applications
-
Excellent interpersonal verbal and written communications skills which are essential in this collaborative work environment
-
Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
-
Ability to be flexible with schedule and work overtime as needed
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses ...
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV hepatitis B hepatitis C and influenza including Harvoni and Sovaldi.
Position: Quality Control Technician I - QC Lab Support
Location: Frederick MD 21704
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift Timings: 7:00am-6:00pm (Sun - Wed)
Job Description:
Responsibilities (include but are not limited to):
-
Receive incoming samples verify documentation and log sample information into LIMS.
-
Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
-
Label store and organize samples according to established procedures and storage requirements.
-
Coordinate sample transfers to internal and external testing labs.
-
Perform routine cleaning maintenance and restocking of sample storage areas.
-
Collaborate with MM QA and other QC functions-including Corporate QC-to support requirements around sampling testing and disposition.
-
Manage and complete all shipping activities within QC functions.
-
Complete routine review of records such as sample chain of custody forms processing logs logbooks and other documentation generated within QC Lab Support.
-
Assist with deviation and investigation activities as needed.
-
Provide updates during daily and weekly meetings.
-
Participate in Lean Lab and other Operational Excellence initiatives.
-
Comply with all safety quality and regulatory guidelines.
-
Perform other duties as assigned.
Basic Qualifications:
-
Bachelors Degree OR
-
AA Degree and 2 years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory OR
-
High School Degree and 3 years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.
Preferred Qualifications:
-
Strong knowledge in applying GMP in QC lab.
-
Exceptional attention to detail and ability to keep track of multiple ongoing projects
-
Proficient in Microsoft Office Excel Visio and other related applications
-
Excellent interpersonal verbal and written communications skills which are essential in this collaborative work environment
-
Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
-
Ability to be flexible with schedule and work overtime as needed
TekWissen Group is an equal opportunity employer supporting workforce diversity.
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