Advanced Research Associate, QC Analyst
Job Details
Experienced
Minneapolis, MN - Minneapolis, MN
Full Time
Bachelor's Degree
None
Day
Quality & Regulatory
Description

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.

Position Summary:

Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, SEC/HPLC, endotoxin assay, TOC, conductivity, pH, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned.

Key Responsibilities:

 

  • Perform, document, and report data for routine QC testing following standard operating procedures.
  • Write and revise standard operating and testing procedures, including instrument qualification and calibration.
  • Collaborate with various departments, including Development, Operations, Process Engineering, and Quality Assurance (QA) to ensure the performance of products. Perform troubleshooting testing as required and assist in writing and implementing change control.
  • Train team members within the department
  • Assist with lab support functions, including instrument calibration and maintenance, reagent ordering and preparation, waste disposal, and laboratory cleaning.
  • Assist with the monitoring of lab supplies and ordering.
  • Perform peer review of laboratory documentation to ensure accuracy and to suggest improvements, as well as to assist in the collection of metrics.
  • Participate in existing or new method validations.
  • Participate in laboratory meetings. Actively take part in meeting with and interacting with group members to learn, provide suggestions for how to make the environment safer, more efficient, and more successful.
  • Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job.
  • Performs additional duties as assigned.
Qualifications

Education and Experience:

  • Position requires a B.S. degree in Biochemistry, Chemistry, Biology, or a related field, and 2 – 5 years related experience with a Bachelors, or 0 – 2 years with a Masters. Industry and GMP experience are preferred. Attention to detail, organization, data analysis and problem-solving skills are required. Must be able to work in a fast-paced environment, multitask, and have good communication skills, both verbally and in writing.

Knowledge, Skills and Abilities:

  • Knowledge of biochemistry and its application to protein, peptide, and antibody products.
  • Knowledge of basic laboratory equipment, QC functions, test procedures and aseptic technique.
  • Knowledge of planning, organizational, and time management tools and the possession of related multi-tasking skills.
  • Knowledge of safety and company rules and policies
  • Knowledge of Microsoft Word and Excel, Internet browsers as well as computer entry and typing skills.
  • Skills in problem solving and critical thinking, including the ability to make effective decisions and execute an appropriate course of action considering all relevant variables and within the scope of defined standard operation procedures.
  • Skills in verbal and written communication, including technical writing skills.
  • Ability to handle sensitive and proprietary information with discretion and confidentiality.
  • Ability to pay attention to details and perform at a high level of accuracy.
  • Ability to learn and consistently execute laboratory tasks.
  • Ability to act independently on routine assignments or on projects with a team.
  • Ability to work in a fast-paced environment.
  • Ability to work hours that confirm to standard business operations (8:00 A.M. to 5:00 P.M.).
  • Flexibility to work alternate or additional hours as needed.

Why Join Bio-Techne:

  • We offer competitive salaries along with extensive medical, vision, and dental plans for you and your family starting on day one!
  • We invest in our employees’ financial futures through 401k matching and an employee stock purchase plan.
  • We help our employees develop their careers through mentorship, promotional opportunities, training and development, 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 foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Where permitted by applicable law, candidate must have received or be willing to receive an FDA authorized COVID-19 vaccine by date of hire to be considered for this position

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

Apply