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 with 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 preventative 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.