Senior Research Associate
Bio-Techne
3 months ago
On-site
Minneapolis, MN
$62,300 - $102,350 USD yearly
Clinical Research and Development
Position Summary
Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern. Plan, execute, and manage activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure objectives are met and products function as expected. Interfaces with Manufacturing, Process Engineering, Product Support, Assay Development, and Quality Assurance.
Key Responsibilities
- Compile, document, interpret, and manage data from ProteinSimple capillary electrophoresis systems (iCE, SimpleWestern) to evaluate in-process materials and finished goods; confirm compliance or identify deviations (functional, assay performance, precision, accuracy). Curate data into established systems.
- Ensure final product meets product requirements and end-user expectations.
- Initiate and support deviation and out-of-specification investigations.
- Recommend corrective actions for problems and processes of all complexities.
- Identify areas for improvement to enhance QC testing and process efficiency.
- Maintain clear and accurate records.
- Attend cross-functional meetings and present data summaries.
- Perform lab work as needed (prepare controls/reagents; run instruments).
- Support projects and new product launch activities; may review unclear factors and provide basic deliverables.
- May support new method validations, establish specifications, and write SOPs.
- May train and provide scientific guidance to others.
- Support other QC operations as needed.
Education And Experience
- Bachelor’s degree in Biology, Chemistry, Engineering, or similar science degree with 5+ years’ experience.
- Master’s degree in Biology, Chemistry, Engineering, or similar relevant experience with 3+ years’ experience.
Knowledge, Skills And Abilities
- Knowledge of basic laboratory equipment and skills (micropipetting, QC functions, test procedures, aseptic technique).
- Apply understanding of electrophoresis techniques and data analysis to troubleshooting or project execution.
- Self-directed learning of new techniques.
- Outstanding analytical skills (R analysis experience a plus).
- Independently perform routine and complex tasks.
- Prioritize and manage multiple tasks.
- Super user level in Excel; proficient in Microsoft Windows.
- Evaluate large volumes of data quickly.
- Strong understanding of quality system regulations/standards.
- Experience in ISO-compliant or other regulated environments.
- Experience developing/reviewing/deploying Standard Work (WI’s, MI’s, SOPs).
- Strong presentation skills.
- Immunoassay methodology experience a plus.
- High work accuracy; meet timelines; collaborate internally; attention to detail.
Benefits (as stated)
- Competitive insurance benefits starting day one: medical, dental, vision, life, short-term disability, long-term disability, pet, legal and ID shield.
- 401k, ESPP, HSA, FSA, Dependent Care FSA.
- Mentorship, training/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.
Application Instructions
- Not accept unsolicited resumes from sources other than a candidate application; unsolicited resumes will be considered company property.
Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern. Plan, execute, and manage activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure objectives are met and products function as expected. Interfaces with Manufacturing, Process Engineering, Product Support, Assay Development, and Quality Assurance.
Key Responsibilities
- Compile, document, interpret, and manage data from ProteinSimple capillary electrophoresis systems (iCE, SimpleWestern) to evaluate in-process materials and finished goods; confirm compliance or identify deviations (functional, assay performance, precision, accuracy). Curate data into established systems.
- Ensure final product meets product requirements and end-user expectations.
- Initiate and support deviation and out-of-specification investigations.
- Recommend corrective actions for problems and processes of all complexities.
- Identify areas for improvement to enhance QC testing and process efficiency.
- Maintain clear and accurate records.
- Attend cross-functional meetings and present data summaries.
- Perform lab work as needed (prepare controls/reagents; run instruments).
- Support projects and new product launch activities; may review unclear factors and provide basic deliverables.
- May support new method validations, establish specifications, and write SOPs.
- May train and provide scientific guidance to others.
- Support other QC operations as needed.
Education And Experience
- Bachelor’s degree in Biology, Chemistry, Engineering, or similar science degree with 5+ years’ experience.
- Master’s degree in Biology, Chemistry, Engineering, or similar relevant experience with 3+ years’ experience.
Knowledge, Skills And Abilities
- Knowledge of basic laboratory equipment and skills (micropipetting, QC functions, test procedures, aseptic technique).
- Apply understanding of electrophoresis techniques and data analysis to troubleshooting or project execution.
- Self-directed learning of new techniques.
- Outstanding analytical skills (R analysis experience a plus).
- Independently perform routine and complex tasks.
- Prioritize and manage multiple tasks.
- Super user level in Excel; proficient in Microsoft Windows.
- Evaluate large volumes of data quickly.
- Strong understanding of quality system regulations/standards.
- Experience in ISO-compliant or other regulated environments.
- Experience developing/reviewing/deploying Standard Work (WI’s, MI’s, SOPs).
- Strong presentation skills.
- Immunoassay methodology experience a plus.
- High work accuracy; meet timelines; collaborate internally; attention to detail.
Benefits (as stated)
- Competitive insurance benefits starting day one: medical, dental, vision, life, short-term disability, long-term disability, pet, legal and ID shield.
- 401k, ESPP, HSA, FSA, Dependent Care FSA.
- Mentorship, training/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.
Application Instructions
- Not accept unsolicited resumes from sources other than a candidate application; unsolicited resumes will be considered company property.