QA Specialist I/II

Artech Information System LLC; Emeryville (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading IT Staffing Company is seeking a dedicated QA Specialist to support quality compliance in manufacturing operations. The ideal candidate will have experience in fermentation processes, analytical testing, and microbiological methods. Responsibilities include providing QA support on the shop floor during manufacturing, troubleshooting issues, and ensuring compliance with quality regulations. Strong analytical skills and proficiency in MS Office are essential for this role, which contributes directly to production quality assurance.

Qualifications

• Experience in fermentation processes using E.coli, yeast, or cell culture.
• Familiarity with analytical testing methods such as HPLC and ELISA.
• Understanding of microbiological methods affecting production processes.

Responsibilities

• Provide QA support during routine operations in Manufacturing.
• Perform independent quality reviews of the Manufacturing process.
• Troubleshoot problems using root cause analysis techniques.

Skills

Fermentation processes using E.coli, yeast, cell culture

Analytical testing methods (Lowry, Bradford, HPLC)

Microbiological methods (bioburden, Sterility, Endotoxin)

Strong scientific analytical skills

Proficiency in MS Word, MS PowerPoint, MS Excel

Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

• The QA Specialist will work as a team member of the Upstream Quality Assurance Production Process Unit to support all aspects of quality related to the manufacture of products.
• Primary responsibility is to provide Shop Floor QA support during routine operations in the Manufacturing area
• Support Manufacturing activities during scheduled shifts. This will require and include weekend support.
• Independently and in some cases, with guidance from senior management, provides quality advice to Manufacturing and Quality groups regarding on-going manufacturing and testing.
• Ensures compliance to documents that govern Manufacturing and Quality operations.
• Performs an independent quality review of the work performed by Manufacturing and Quality groups. (BPD, TRF, Logbook)
• Perform minor deviation investigations and follow up to ensure timely resolution or escalation, if deemed necessary during the process of investigation.
• Performs and reviews minor deviation investigations and coordinates with QA team to ensure closure and disposition of impacted products.
• Assist with investigations related to suppliers for their designated production area.
• Troubleshoot problems in their assigned production process unit, identify and isolate causal factors through effective root cause analysis techniques and proactively innovate new and effective strategies for problem resolution solutions.
• May interact with regulatory and partner auditors/inspectors during tours.
• Comply Site Environmental Health & Safety (EH&S) requirements

Qualifications

• Must have \experience in one or more of the main areas listed:
• Fermentation processes using E.coli, yeast,cell culture or other organisms
• Analytical testing methods such as Lowry, Bradford, BCA, SDS-PAGE, Western Blot, HPLC, Amino Acid Analysis, ELISA's and in vitro diagnostic test kits for the analysis of finished products.
• Microbiological methods such as Microbial Limits Test (bioburden), Sterility, Endotoxin, TOC, Microbial Identification, Contamination testing that may impact production processes.
• Manufacture of Bacterial and Yeast Seedstocks
• Environmental/Utility/facility Monitoring programs and impact to production facilities
• Equipment qualification, calibration and preventitive maintenance programs
• Experience in one or more validation areas: Process, Cleaning, Facilities, Utilities and Equipment validation
• Strong scientific analytical skills, proficient in MS Word, MS PowerPoint and MS Excel software.
• Must be familiar with GMP's and Quality System Regulations (QS Regs).
• Must have good planning and organizing skills, manage time effectively by prioritizing tasks, taking the initiative to solve problems quickly, and knowing when to obtain assistance.