QC/GMP Clinical Technician (ONSITE)(1st Shift)

Please note that this is a 1-year contract.

• This will be a first shift position 7-3:30 AM with flexibility to work weekends, over time and fluctuation on start time (a couple of hours earlier or later) to accommodate business needs.
• Weekends and OT is occasionally required

Qualifications:

• Responsible for performing quality control testing according to established procedures and timelines.
• Required A Bachelor's degree in Medical Technology, Biology, Chemistry or a related field of study and a minimum of 1-3 years’ experience with QC, GMP, and analytical procedures is required. 
• Experience with analytical instrumentation such as AutoVue and ProVue is preferred. 
• Guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred. 
• Manual dexterity to handle instruments, complete repetitive motions, and stand for long periods of time is required. 
• Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. 
• Excellent oral and written communication skills are required. 
• Proficiency with the Microsoft Office suite of products (Excel, Word, PowerPoint, Outlook).

Responsibilities:

• Responsible for performing in-process testing all types of BioVue cassettes.
• Assure compliance with company standards and applicable regulatory agencies. 
• Participate in failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures.
• Perform testing within established timelines in accordance with current cGMP’s. 
• Participate in equipment maintenance/calibration program. 
• Ability to prioritize and handle multiple tasks and challenges at one time and have the ability to work in a team environment and provide customer focused results in an efficient manner.

Applicants must provide their phone number. Reference job number A4791.