- Perform, document and report routine QC testing following standard operating procedures
- Analyze assay data and perform routine troubleshooting of products with internal and external customers
- Generation of technical reports and effectively communicating results to team members and key stakeholders
- Monitor product and laboratory documentation
- Keep accurate records of all experiments performed
- Follow GxP guidelines, documentation, and workflow
- Assist with lab support functions, including instrument calibration and maintenance, reagent ordering and preparation, waste disposal, and laboratory cleaning
- Participate in new method validations, group projects and meetings
- 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 plans
- Follow 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 with the role
- Assist with lab support functions, including instrument calibration and maintenance, reagent ordering and preparation, waste disposal, and laboratory cleaning
- Keep accurate records of all experiments performed
- Follow GMP guidelines, documentation, and workflow
- Support technical services and other departments by providing pertinent information and recommendations, and by performing lab procedures to resolve customer complaints or other issues
- Author, update, and validate SOPs and methods as appropriate
- Participate in lab meetings and train team members within the department
- Follow 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 with the role
- Bachelor's degree in the biological sciences or equivalent, with 6 to 8 years of related laboratory experience
- OR a Master's degree with 3 to 5 years of related laboratory experience
- Attention to detail, organization, data analysis and problem-solving skills are required
- Industry and GMP experience are preferred
- Must be able to work in a fast-paced environment, multi-task, and have good communication skills, both verbally and in writing
- Working knowledge of Microsoft Word and Excel is required
- Knowledge of cell biology, biochemistry, protein chemistry, lab equipment and QC functions
- Demonstrate proficiency in biophysical analytical laboratory techniques including, but not limited to, liquid chromatography methods, immunoassays, protein mass analysis and light scattering
- Ability to plan, organize and manage time independently to accomplish multiple concurrent tasks
- Ability to pay attention to details and perform at a high level of accuracy in laboratory processes and record keeping skills (lab notebook and technical writing) are essential
- Ability to effectively problem solve and think critically, 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
- Ability to learn and consistently execute laboratory tasks
- Ability to adhere to the company's safety policy
- 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 act independently on routine assignments or collaboratively on projects with the team
- Ability to work hours that adhere to standard business operations (8:00 A.M. to 5:00 P.M.)
- Flexibility to work alternate or additional hours as needed
- 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.
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Senior Research Associate - Minneapolis, United States - Bio-Techne
Description
Job DetailsLevel:
Experienced
Job Location:
Minneapolis MN - Minneapolis, MN
Position Type:
Full Time
Education Level:
Bachelor's Degree
Salary Range:
Undisclosed
Travel Percentage:
Negligible
Job Shift:
Day
Job Category:
Quality & Regulatory
Description
By joining the Bio-Techne team, you will have an impact on future cutting-edge research. Bio-Techne and all of its brands provides tools for researchers in Life Sciences and Clinical Diagnostics.
Position Summary:
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Senior Research Associate in the Analytical Services team, you will not only lead routine Quality Control (QC) testing, but also lead investigations and troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies using a wide variety of tools including capillary electrophoresis systems, chromatography, immunoassays, light scattering and other analytical tools, with and without the aid of fully defined SOPs.
You will also actively take part in group projects, lead process improvement efforts to improving lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned.
Key Responsibilities:
Education and Experience:
Knowledge, Skills, and Abilities:
Why Join Bio-Techne:
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.