By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

$23.20 - $31.90

Summary:  Responsible for performing area line clearances for multiple departments, various types of physical/visual inspections, various types of verifications, environmental monitoring, identifying trends, and assisting in process improvement

Duties and Responsibilities:

Perform area line clearances for multiple departments as needed

Perform various types of visual/dimensional/functional inspections and verifications for incoming raw materials, in-process and finished products, labels, inserts and other related materials for multiple departments and while recognizing and documenting trends as needed

Perform vial count verifications and in-process label confirmations for Production as needed

Perform environmental/equipment monitoring as needed (i.e. Controlled Environment Room, temperature monitoring)

Write Standard Operating Procedures (SOP’s) when appropriate

Initiate Non-Conforming Material Reports when appropriate

Initiate Change Order forms when appropriate

Ensure compliance with Good Manufacturing Practice (GMP) / Good Documentation Practice (GDP)

Follow SOPs to perform all Quality Control inspections and verifications

Inform management and other personnel of quality problems, failures and deviations

Identify and implement quality system improvements and providing feedback when appropriate

Perform special request inspections and rework projects as required

Assist in the control and maintenance of documents associated with Quality Control activities. Initiates document updates through the Document Control system.

Provide additional support for the Quality Control Department to ensure effective operations

Perform other duties, additional functions and/or special projects as assigned

Knowledge, Skills and Abilities Required:

Detail oriented

Strong understanding of basic mathematics with exposure to statistical techniques

Ability to show initiative and to perform in a multi-task environment

Good interpersonal and verbal/written communication skills

Ability to work with personnel of all levels

Knowledge of Quality System Regulation (QSR) and ISO EN13485

Minimum Job Requirements:

High school diploma or GED. 

Minimum 1 year of cGMP experience in a medical/diagnostic or related industry production setting

Why Join Bio-Techne:

We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.