Research Associate, Analytical QC

Bio-Techne•Minneapolis, MN

2d•Onsite

About The Position

The Research Associate, Analytical QC will 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, endotoxin assay, TOC, conductivity and other testing as assigned. 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.

Requirements

B.S. degree in Biochemistry, Chemistry, Biology, or a related field
0 - 2 years related experience
Attention to detail
Organization
Data analysis
Problem-solving skills
Ability to work in a fast-paced environment
Multitask
Good communication skills, both verbally and in writing
Knowledge of biochemistry and its application to protein, peptide, and antibody products.
Knowledge of basic laboratory equipment, QC functions, test procedures and aseptic technique.
Ability to plan, organize, and manage time.
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.

Responsibilities

Perform, document, and report data for routine QC testing following standard operating procedures.
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 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.

Benefits

competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
401k plans
employee stock purchase plan (ESPP)
Health Saving Account (HSA)
Flexible Spending Account (FSA)
Dependent Care FSA
mentorship
promotional opportunities
training and development
tuition reimbursement
internship programs
employee resource groups
volunteer paid time off
employee events
charity drives
accrued leave policy with paid holidays, paid time off, and paid parental leave.