QC/GMP Bloodborne Manufacturing (ONSITE)

Please note that this is a 1-year contract position.

Qualifications:

• 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. Familiarity with the 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.

The successful candidate will have the 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 A4936