· 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:

· 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.

· 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.