Top 28 Principal scientist, microbiology Jobs in River Falls Wi

Senior Principal Quality Engineer
Vantive —Oakdale, MN
- $120,000 - $165,000 a year
- 5 years
- Engineering
- Analysis skills
- Paid parental leave
- Paid holidays
Food Safety & Quality Assurance Manager (S1268)
Wellness Pet Company —South Saint Paul, MN
- $110,000 - $140,000 a year
- Full-time
- 5 years
- Organizational skills
- Senior level
- Paid parental leave
- AD&D insurance
Quick Apply
Principal Scientist, Microbiology
The U.S. Pharmacopeia (USP) —Saint Paul, MN
- $138,123 - $173,900 a year
- Full-time
- 11+ years
- Doctor of Philosophy
- Mentoring
- Paid time off
Medical Laboratory Scientist (MLS) - Straight Evenings
Emergency Physicians Professional Association —Woodbury, MN
- $37.55 an hour
- Evening shift
- Clinic experience
- Mid-level
- Bachelor's degree
Medical Laboratory Scientist
Fairview Health Services —Maplewood, MN
- $37.37 - $52.76 an hour
- Weekends as needed
- Acute care
- Hospital
- Customer service
Associate Director, Lab Operations-Pharma (GMP)
Pace Analytical Services —Oakdale, MN
- $115,000 - $130,000 a year
- Full-time
- Bachelor's degree
- Senior level
- Leadership
- Wellness program
- Health savings account
Medical Lab Technician (MLT)
HUDSON PHYSICIANS SC —Hudson, WI
- OSHA
- Word processing
- Computer literacy
Quick Apply
Medical Laboratory Scientist
Regions Hospital —Saint Paul, MN
- $33.29 - $49.93 an hour
- Full-time
- Hospital
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
2d
PLS Associate Scientist I - Microbiology
Pace Analytical Services —Oakdale, MN
- $22 - $24 an hour
- Full-time
- Customer service
- English
- Project management
- Wellness program
- Health savings account
Medical Laboratory Technician
Fairview Health Services —River Falls, WI
- $27.88 - $39.36 an hour
- Weekends as needed
- Urgent Care
- Mid-level
- Mentoring
Director Product Research & Development
Dairy Management Inc. —Saint Paul, MN
- $100,000 - $125,000 a year
- Full-time
- Hybrid work
- Office
- Doctor of Philosophy
- Senior level
- Paid parental leave
- Disability insurance
Quick Apply
Sterility Assurance Program Manager
Bio-Techne —Saint Paul, MN
- $78,100 - $128,500 a year
- Weekends as needed
- 5 years
- Ability to lift 50 pounds
- Analysis skills
- Paid parental leave
- Health savings account
2d
Medical Laboratory Technologist (MLT) - Straight Evenings
Emergency Physicians Professional Association —Woodbury, MN
- $30.06 an hour
- Evening shift
- Float pool
- Clinic experience
- Mid-level
VP Quality, Global Life Sciences
Ecolab Inc. —Saint Paul, MN
- $249,500 - $374,300 a year
- Overtime
- Organizational skills
- Fair chance
- Manufacturing
- Opportunities for advancement
Medical Laboratory Technician
HealthPartners/GHI —Woodbury, MN
- $28.84 - $36.17 an hour
- Full-time
- English
- Clinic
- Conflict management
19h
Quality Engineer I
Abbott Laboratories —Saint Paul, MN
- $50,700 - $101,300 a year
- Full-time
- Engineering
- Mid-level
- Computer skills
- Health insurance
- Tuition reimbursement
Sr. Principal Engineer - Digital Solutions
Vantive —Oakdale, MN
- $128,000 - $160,000 a year
- 5 years
- Travel
- SharePoint
- Paid parental leave
- Paid holidays
Laboratory Care Technician
Fairview Health Services —Maplewood, MN
- $21.84 - $30.83 an hour
- Part-time
- 18 years or older
- Hospital
- Customer service
13d
Senior Principal AI Scientist
Recruits Lab —United States
- $185,000 - $280,000 a year
- Full-time
- Doctoral degree
- Research
- Senior level
- Paid holidays
- Disability insurance
Quick Apply

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Senior Principal Quality Engineer

Vantive -
Oakdale, MN

Apply Now

Job Details

$120,000 - $165,000 a year

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Employee discount

Qualifications

Microbiology
Analytical chemistry
Pharmaceutical regulatory compliance
Microbiology
Pharmaceutical company experience
Biomedical regulatory compliance
GMP for research safety and compliance

Full Job Description

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Your Role

The Senior Principal Quality Engineer is responsible for leading quality support and sustaining activities for Drug Products & Medical Device Research & Development activities related to laboratory testing, product validations, and QMS documents management in support of therapeutics products. This role is part of a team of approximately 50 scientists and engineers in Vantive that is building up capability and laboratories in Oakdale, MN, and will be located onsite at least 3 days per week with the team.

What you'll be doing:

Act as the primary Quality Subject Matter Expert (SME) for drug product and medical devices related activities at the on-site laboratories, working closely with the Quality Manager and the local R&D team to establish local procedures in compliance with international regulations such as EU MDR, as well as the monitoring of local compliance to the Vantive Quality Management System (QMS).
Review and approve site generated QMS documentation, including but not limited to verification and validation protocols and reports, equipment qualifications, studies, procedures, training plans, change control activities, laboratory investigations, equipment out of tolerance and other quality documentation related to local drug product and medical device R&D activities.
Support site readiness for and participate in audit activities for the Drugs Products and Sciences R&D groups by developing audit plans, executing internal audits along with Quality Manager, and acting as a Quality SME for external audits, such as those for EU GMP regulation.
Perform quality-related functions for activities such as Nonconformance Investigation and Corrective and Preventive Action (CAPA) Management.
Work with other R&D sites to harmonize QMS related laboratory practices and procedures, as well as applicable training.

What you’ll bring:

Required Skills

Bachelor's Degree in a related field and 6+ years of relevant experience in the medical device or pharmaceutical industry or a similarly regulated industry. 5+ years of experience working in and/or supporting an analytical chemistry or microbiology lab in support of regulated products, such drug products.
Ability and willingness to work independently, communicate effectively, make decisions, and promote compliance to company QMS as a Quality representative for the site.
Must have familiarity with standard laboratory procedures and requirements under GLP/GMP regulations.
Demonstrated understanding in general principles of Quality Engineering and worldwide Quality System standards and regulations.

Preferred Skills

Experience with EU GMP (EudraLex Vol 4.) and ISO 13485 highly preferred
Experience with ISP and USP Guidelines and Standards highly preferred
Bachelor’s degree in engineering or a Science discipline
Formal Audit training or certification
American Society for Quality Certification (e.g., CQE, CQA, etc.) and/or Six Sigma certification highly preferred
Experience / understanding of Risk Management techniques and principles
Ability to work under deadlines and changing priorities with minimal supervision
Team player with excellent verbal and written communication skills to work cross-functionally in a highly matrixed organizational environment
Strong analytical and problem-solving skills
Understanding of scientific method and application of science to test method development and validation highly preferred.
Ability to multitask, working on multiple projects and work activities running in parallel.

Vantive is committed to supporting the need for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $120,000 to $165,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

US Benefits at Vantive

This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive’s 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals.

We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive’s US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive

Equal Employment Opportunity

Vantive is an equal opportunity employer. Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

Recruitment Fraud Notice

Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Apply Now

Refine Your Search

principal scientist, microbiology jobs in river falls wi

Senior Principal Quality Engineer

Food Safety & Quality Assurance Manager (S1268)

Principal Scientist, Microbiology

Medical Laboratory Scientist (MLS) - Straight Evenings

Medical Laboratory Scientist

Associate Director, Lab Operations-Pharma (GMP)

Medical Lab Technician (MLT)

Medical Laboratory Scientist

PLS Associate Scientist I - Microbiology

Medical Laboratory Technician

Director Product Research & Development

Sterility Assurance Program Manager

Medical Laboratory Technologist (MLT) - Straight Evenings

VP Quality, Global Life Sciences

Medical Laboratory Technician

Quality Engineer I

Sr. Principal Engineer - Digital Solutions

Laboratory Care Technician

Senior Principal AI Scientist

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