QC Analyst 2

Join us in developing pioneering therapies that aim to transform the treatment of CKD and change patients' lives. Our technology is designed to treat diseased kidneys using a patient's own cells and may prevent or delay dialysis or transplant.

• Supports the weekly environmental monitoring and post sampling incubation and enumeration of plates.
• Reads, understands, and follows Standard Operating Procedures (SOPs)
• Assists in the training and mentoring of new staff.
• Sets up and operates quality control equipment including cell counters, centrifuges analytical balances and coordinates the maintenance of these equipment with the facility personnel.
• Assists in deviation and OOL investigations, and compiles data/information related to internal investigations as required.
• Revises approved documents as required including SOPs, testing forms, and MS forms and reviews document updates for accuracy and completeness.
• Perform routine transactions with the ERP system including, but not limited to material requisitions and submission of PR's for outside testing labs.
• Responsible for follow-ups with the outside testing labs regarding delay in availability of test reports or any other issues with sample submissions.
• Complete GMP documentation, including testing forms, logbooks according to GDP
• Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
• Ensure that all team members comply with safety rules and regulations.
• Able to perform procedures according to written guidelines and recognize a deviation from accepted practice.
• Relies on instructions and pre-established guidelines to perform the functions of the job.
  
  

Requirements

Description

Education/Training

BS in Microbiology, Biology, Chemistry, or equivalent required

Preferred area of study: Science related discipline

Experience

Minimum 5+ years relevant experience

Skills/Abilities

• Ability to exercise judgment within defined procedures and practices to determine appropriate action.
• Ability to read, understand and follow schedule.
• Ability to read, understand and follow SOP's.
• Ability to understand the importance of compliance with cGMP's.
• Ability to follow GLP daily.
• Ability to work independently as well as in a team setting.
• Computer software skills including Microsoft Office
• Organization skills, record keeping, time management, regular attendance
  
  

Other

• Good eye/hand coordination
• Written and oral communication, team oriented, strong work ethic
  
  

ProKidney is an Equal Opportunity Employer. All applicants are considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We are committed to the principles of equal employment opportunity for all employees with a work environment free of discrimination and harassment.