Research Associate - GMP Purification

Bio-Techne•Minneapolis, MN

1d•$40,300 - $66,250•Onsite

About The Position

This position is responsible for the purification of proteins and polyclonal/monoclonal antibodies in a GMP laboratory environment while adhering to Good Manufacturing Practice (GMP) guidelines. The role supports the production of GMP, ACFP, natural, and other products utilized by pharmaceutical and IVD customers. Responsibilities include protein and antibody purification through column chromatography and related techniques, aseptic filtration and bottling activities, inventory submissions, and completion of GMP-compliant documentation.

Requirements

Requires a bachelor’s degree in Biochemistry, Biotechnology, Biology, Chemistry, or a related scientific discipline and 0–2 years of relevant laboratory experience.
GMP regulations, laboratory documentation practices, and controlled environments.
Protein and antibody purification methods and chromatography principles.
Laboratory safety procedures and chemical handling requirements.
Microsoft Office applications, including Word, Excel, and Outlook.
Performing laboratory procedures with precision and attention to detail.
Technical documentation, recordkeeping, and data management.
Planning, organization, time management, and multitasking.
Building effective working relationships and collaborating across teams.
Written and verbal communication, including technical writing.
Follow detailed procedures and maintain compliance with GMP standards.
Work independently while managing multiple priorities.
Handle confidential and proprietary information with discretion.
Adapt to changing business and production priorities.
Maintain a high level of accuracy in a regulated laboratory environment.

Nice To Haves

Experience with chromatography techniques is preferred.

Responsibilities

Purify proteins and polyclonal/monoclonal antibodies using column chromatography and associated purification techniques.
Perform filtration, aliquoting, and bottling of products using aseptic laboratory practices.
Complete batch records and manufacturing documentation in accordance with GMP requirements.
Assist with GMP bottling and production activities as needed.
Clean and validate laboratory equipment and procedures to maintain audit readiness.
Support internal and external audits by ensuring laboratory compliance and organization.
Revise specifications, standard operating procedures (SOPs), and controlled documents; submit revisions for management review and approval.
Monitor inventory levels of chemicals, raw materials, consumables, and stock buffers; initiate replenishment requests as needed.
Ensure equipment calibrations and laboratory maintenance activities remain current.
Utilize Microsoft Office applications, including Word, Excel, and Outlook, to support documentation and communication needs.
Maintain confidentiality of sensitive, proprietary, and regulated information.
Follow all company policies, safety procedures, AWAIR requirements, Chemical Hygiene guidelines, and Exposure Control procedures.
Perform additional duties and projects 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
paid parental leave