Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions tour clients world-wide. The below job opportunity is with one of our Biotech clients whresearches 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 Chemist
Location: Frederick MD 21704
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Wednesday- Saturday (07.00AM-5.30PM)
Description:
Responsibilities (include but are not limited to):
- Perform testing of raw materials intermediates and final products by following analytical methods: Cell based bioassays Flow Cytometry ELISA and qPCR assays.
- Work with internal and external resources to maintain lab in an optimal state.
- Assist with monitoring and trending data complete routine record review of test data and related documents for in-process testing drug substance and drug product release.
- Supply information to support generation of CoAs for product release.
- Maintains laboratory instruments for calibration and routine maintenance
- Author or revise SOPs qualification/validation protocols and reports.
- Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.
- Provide updates at daily and weekly meetings.
- Monitor the GMP systems currently in place to ensure compliance with documented policies.
- Review proposed changes to systems procedures methods and submissions to regulatory agencies as appropriate.
- Gather metric information for use in continuous improvement of areas of responsibility.
- Perform other duties as required.
Basic Qualifications:
- Bachelors Degree OR
- AA Degree and 2 years experience in biotechnology or related field and Quality Control experience OR
- High School Degree and 3 years experience in biotechnology or related field and Quality Control experience
Preferred Qualifications:
- Strong knowledge of GMP SOPs and quality control processes.
- Identifying writing evaluating and closing OOSs and investigations.
- Proficient in MS Word Excel Power Point and other applications.
- Strong written and verbal communication skills.
- Ability to communicate and work independently with scientific/technical personnel.
- Well versed in various analytical techniques such as Flow Cytometry ELISAs PCR and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
- Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
- Preferred: Experience in the biotech and/or pharmaceutical industry.
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 tour clients world-wide. The below job opportunity is with one of our Biotech clients whresearches develop and commercializes drugs. The company focuses primari...
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions tour clients world-wide. The below job opportunity is with one of our Biotech clients whresearches 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 Chemist
Location: Frederick MD 21704
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Wednesday- Saturday (07.00AM-5.30PM)
Description:
Responsibilities (include but are not limited to):
- Perform testing of raw materials intermediates and final products by following analytical methods: Cell based bioassays Flow Cytometry ELISA and qPCR assays.
- Work with internal and external resources to maintain lab in an optimal state.
- Assist with monitoring and trending data complete routine record review of test data and related documents for in-process testing drug substance and drug product release.
- Supply information to support generation of CoAs for product release.
- Maintains laboratory instruments for calibration and routine maintenance
- Author or revise SOPs qualification/validation protocols and reports.
- Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.
- Provide updates at daily and weekly meetings.
- Monitor the GMP systems currently in place to ensure compliance with documented policies.
- Review proposed changes to systems procedures methods and submissions to regulatory agencies as appropriate.
- Gather metric information for use in continuous improvement of areas of responsibility.
- Perform other duties as required.
Basic Qualifications:
- Bachelors Degree OR
- AA Degree and 2 years experience in biotechnology or related field and Quality Control experience OR
- High School Degree and 3 years experience in biotechnology or related field and Quality Control experience
Preferred Qualifications:
- Strong knowledge of GMP SOPs and quality control processes.
- Identifying writing evaluating and closing OOSs and investigations.
- Proficient in MS Word Excel Power Point and other applications.
- Strong written and verbal communication skills.
- Ability to communicate and work independently with scientific/technical personnel.
- Well versed in various analytical techniques such as Flow Cytometry ELISAs PCR and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
- Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
- Preferred: Experience in the biotech and/or pharmaceutical industry.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
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