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We are not offering you a job, but rather we are offering you a workplace that feels like home at Greiner Bio-One.

Quality Control Supervisor - Preanalytics

Location: 

Monroe, US, 28110

Travel activity:  NA
Employment Type:  Permanent

Your challenge

•    Leadership (supervision and mentorship) of various direct-report teams
•    Tracking attendance of direct reportsCoordinate daily activities to meet departmental KPI’s
•    Support quality validations activities 
•    Follow appropriate steps for the identification and handling of nonconforming product
•    Release of Incoming Goods Inspections according to valid procedure(s)
•    Review and approval of half-finished and finished Vacuette products according to valid procedure(s)
•    Complete required activities in SAP such as transfers, review, quality hold and releases
•    Organize and perform special testing in cooperation with QCM PA-L
•    Perform training and retraining for QC and production personnel
•    Preparation, edition, and distribution of quality or related documents 
•    Perform periodic inventory and order laboratory supplies as needed
•    Support maintenance of testing equipment in laboratory and manufacturing including scheduling and/or performance of internal/external calibrations as required
•    Support administrative duties as assigned
•    Support for In-process inspections and in-coming goods inspections as needed 
•    Other duties as assigned
Authority includes:
•    Training of new and/or existing QC employees regarding QC procedures and use of equipment 
•    Release/scrap ERP transactions of product according to valid procedures
•    Evaluation of products according to valid procedures
•    Review of and corrections to related QIRs in cooperation with QCM PA-L, Q-ENG-L or designee

Your Profile

•    Bachelor’s Degree in Science, life sciences, or related field; Bachelor’s Degree is preferred
•    3 years of relevant leadership experience in a medical device (ISO 13485 preferred) or similar manufacturing environment 
•    2 years GMP, GDP, and GLP work experience in a Quality Control laboratory setting
•    Advanced-level experience with laboratory testing equipment, instrumentation, and analysis, as well as laboratory data processing and review
•    Intermediate-level experience with CAQ (Computer Aided Quality) inspections systems
•    Intermediate-level MS office skills and communication & data management computer skills
•    Intermediate-level knowledge with basic statistic and calculations; proficient knowledge in applicable chemical calculations preferred

Physical Requirements:
•    Must be able to stand and walk for up to 8-12 hours
•    Must be able to lift up to 70 lbs
•    Must have appropriate vision to perform detailed quality inspections as outlined in SOP’s or TP’s

As an employer, we stand for equal opportunities and all qualified applicants are considered regardless of race, religion, creed, color, sex, sexual orientation, gender identity, genetic information, age national origin, veteran status, physical or mental disability or any other characteristics protected under applicable federal, state or local law. We have set ourselves the goal of increasing the proportion of women in managerial and expert positions and therefore encourage qualified women to apply.
Job ID:  2223

About Greiner Bio-One

Greiner Bio-One feels like home.

For visionaries with drive and ideas, for team players who share their knowledge and entertain new ways of thinking, for people who strive for excellence. Our door is always open to achievers, doers and hidden talents who want to make a difference.

We have future in our blood.


Nearest Major Market: Charlotte

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