Quality Control Chemist

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Work Schedule:
Wed-Sat

This position's starting pay is: $26.00/hr.

IMPORTANT: For the first 7 weeks of the assignment, all contractors are required to work Mon-Fri ) to complete New Hire Orientation and Manufacturing On-boarding Technical Training. After the 7 weeks, the contractor is deployed onto their agreed upon shift. New hires will need to complete

Work Arrangement:
Onsite - Shift flexibility preferred

Position Summary:

Perform testing of raw materials, intermediates and final products by following analytical methods:
Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.

Key Responsibilities:

• 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.

Qualifications &

Experience:

• Bachelor’s 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 OOS’s and investigations.
• I am 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.
• For information on benefits, equal opportunity employment, and location-specific applicant notices,

At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws.

• Associate

• Contract

• Analyst and Manufacturing
• Industries Pharmaceutical Manufacturing and Biotechnology Research

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