Why Mayo Clinic

Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans (https://jobs.mayoclinic.org/benefits/) – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. You’ll thrive in an environment that supports innovation, is committed to ending racism and supporting diversity, equity and inclusion, and provides the resources you need to succeed.

Responsibilities

Join Mayo Clinic on its path to finding cures and become part of the legacy that enables us to provide the best care to patients from all over the world!

Formally reports to and receives direction from an identified supervisor in Mayo Clinic Center for Regenerative Biotherapeutics (CRB). Works collaboratively with advanced biomanufacturing, process development, quality, and regulatory staff, as well as Mayo Clinic Principal Investigators and external partners to formulate and establish product performance objectives. The role will work closely with process development and technical transfer and manufacturing staff to meet upstream and downstream outcomes including in-process, release and stability testing, leading assay development and validation and driving quality control documentation and investigations. The position requires a hands-on approach, being able to work on teams and establish good working relationships with other departments or partners both internally and externally.

The Quality Control Senior Engineer is responsible for performing, analyzing and investigating quality control assays, including in-process, release and stability tests, and assay development tasks as directed by supervisor, providing qualification and validation support for manufacturing processes that are essential to the clinical production.

Perform all GMP related activities strictly according to SOPs with accurate and complete documentation associated with the testing, in compliance with cGMP, principles of Data Integrity and good documentation practices. Performs and implements investigations and process improvements including CAPAs and Change Controls. Ensures compliance with all applicable Federal and State accrediting agency requirements in the testing of biopharmaceutical products manufactured in the current Good Manufacturing Practices (cGMP) facility. Leads in optimization and validation of new analytical procedures for testing as necessary and is a subject matter expert (SME) in one or more areas. Responsible for developing, reviewing and revising Standard Operating Procedures as necessary. Perform general laboratory activities as assigned by supervisor. Complete and maintain updated all training required to perform assigned tasks and develops and implements training for others. Performs audits of processes and data and SME for external audits..

Qualifications

A master’s degree in a biomedical related field (biology, chemistry/biochemistry, laboratory medicine, etc.) with at least 2 years research experience within a laboratory environment; or a bachelor’s degree in a biomedical related field and a minimum of 5 years relevant experience. cGMP environment work experience in clinical manufacturing of biologics or products intended for human use is preferred.

Must have strong technical understanding and experience developing assays. Ability to analyze data and compose reports. Ability to effectively communicate complex ideas to a variety of shareholders across functions through multiple forms of communications. An understanding of the application of laws, regulations, and guidance documents related to FDA regulated biologics, pharmaceuticals, devices, etc. Exceptional human relations and communication (written, verbal, and listening) skills. Flexibility and capable of adapting to and facilitating change. Must demonstrate capacity to comprehend complex protocols, programs, and situations. Ability to exercise good judgment while working under deadlines is required.

Must be flexible with work schedule as needed to meet internal and external customer needs.

Visa sponsorship is not available for this position.

Exemption Status

Exempt

Compensation Detail

$74,859.20 - $112,195.20 / year

Benefits Eligible

Yes

Schedule

Full Time

Hours/Pay Period

80

Schedule Details

Monday through Friday, occasional weekends to support manufacturing.

Weekend Schedule

Occasional

International Assignment

No

Site Description

Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. (https://jobs.mayoclinic.org/alllocations)

Affirmative Action and Equal Opportunity Employer

As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.

Recruiter

Chelsea Crosby

Equal opportunity

As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.