| Open Until Filled | Yes |
|---|---|
| Description of Work |
The Biological Process Development Facility (BPDF) is looking for a purification team member to join our production group. This position will participate in purification process scale-up and optimization to foster the development of therapeutic proteins and other biologics. This position is expected to apply technical and functional knowledge to assist in experiment/project design that will enable the purification team to meet its goals.
Job Duties include: · Design and execute purification scale-up and optimization activities related to the production of therapeutic proteins following GLP (Good Laboratory Practice)/GMP (Good Manufacturing Practice).
· Perform tasks in preparation of and during actual purification runs consisting of equipment preparation, calibration, cleaning, column packing, evaluation and cleaning, solution preparation, processing and system operation.
· Monitor and troubleshoot development, engineering, and production runs in the development labs and GMP facility.
· The position will troubleshoot, design and complete experiments based on data from previous experiments, write scientific reports, and communicate with supervisors.
· Assist in equipment maintenance.
· Assist with culture harvest and cGMP fermentation.
The BPDF provides biopharmaceutical process development and biomanufacturing services that transition discoveries into early phase clinical trials. The BPDF produces a wide range of biologics- including vaccines, recombinant proteins gene therapies and other biotherapeutics – in partnership with government agencies, biotechnology companies, academic researchers, and non-profit organizations. This position offers a great opportunity to learn Good Manufacturing Practice (GMP) principles and further develop your technical skills and knowledge of biotherapeutic production. Join our tightly knit collaborative team and play a key role in advancing the development of life-changing biopharmaceuticals.
Ranked as one of the best employers in the state of Nebraska, the University of Nebraska is committed to providing a work environment and culture that fosters personal and professional success and satisfaction. By joining our team, you will have the opportunity to grow as an individual and contribute to the significant impact that we make within the university of Nebraska community, Nebraska’s economy, and the lives of individuals across the US and around the globe.
We invest in our employees:
The University of Nebraska-Lincoln seeks to attract and retain a high performing and collaborative workforce. UNL is committed to providing a work environment and culture that fosters personal and professional success where every person and every interaction matters. The University is proud to be one of Nebraska’s preferred and largest employers where individuals are able to participate and contribute to their full potential.
As an EO/AA employer, qualified applicants are considered for employment without regard to race, color, ethnicity, national origin, sex, pregnancy, sexual orientation, gender identity, religion, disability, age, genetic information, veteran status, marital status, and/or political affiliation. See: http://www.unl.edu/equity/notice-nondiscrimination |
| Minimum Required Qualifications |
Bachelor’s degree in life sciences/chemical or chemical/biomolecular engineering and two years of experience in a lab environment. Must possess knowledge of the operation principles of purification such as column chromatography, tangential flow filtration, and pump operation. Knowledgeable and experienced in basic laboratory equipment. Knowledge of GLP/GMP requirements for production of biopharmaceuticals. Ability to work well with others in a team environment.
Candidates for this position must be a US Citizen, Permanent Resident, Refugee or Asylee in order to work on projects subject to Export Control regulations.
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| Preferred Qualifications |
Master’s degree in life sciences/chemical or chemical/biomolecular engineering and five years of experience in a GLP/GMP biopharmaceutical production facility. Experienced performing purification processes such as column chromatography, and TFF. Experience using aseptic technique. Experience operating in a GLP/GMP environment.
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| Pre-Placement Driving Record Review Required | No |
| Physical Required | No |
| Commercial Driver’s License (CDL) required. Subject to DOT approved pre-employment & random testing for alcohol and controlled substances. | |
| Criminal History Background Check Required | Yes |
| Posted Salary | $44,000/yr. minimum |
| How to Apply |
Click on “Apply for this Job.” You will then either create an application or edit your current application that is on file. You will be required to attach your resume, cover letter, and list of references as three (3) separate documents in MS Word or PDF format.
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| For questions or accommodations related to this position contact |
Cathy Norquest cathy.norquest@unl.edu
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| Job Category (old) | Managerial/Professional |
| Job Type | Full-Time |
| Alternate Work Schedule (if other than 8-5) | May include working evenings and weekends. |
| Work Location (City, State) | Lincoln, NE |
| Position funded by grant or other form of temporary funding? | Yes |
| If Temporary, indicate end date | |
| Planned Hire Date: | |
| Appointment End Date |
Supplemental Questions
Required fields are indicated with an asterisk (*).
Required Documents
Required Documents
- Resume
- Cover Letter
- List of References
Optional Documents
