Maple Grove, MN · On-site
... Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our ... Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V ...
New
Maple Grove, MN · On-site
... Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our ... Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V ...
New
Saint Cloud, MN · On-site
$86K - $107K/yr
As a well-established biotechnology company with a strong reputation for quality, collaboration ... Design and oversee characterization studies, risk assessments, and validation strategies for new ...
Saint Cloud, MN · On-site
$86K - $107K/yr
As a well-established biotechnology company with a strong reputation for quality, collaboration ... Design and oversee characterization studies, risk assessments, and validation strategies for new ...
Saint Cloud, MN · On-site
As a well-established biotechnology company with a strong reputation for quality, collaboration ... Design and oversee characterization studies, risk assessments, and validation strategies for new ...
Saint Cloud, MN · On-site
As a well-established biotechnology company with a strong reputation for quality, collaboration ... Design and oversee characterization studies, risk assessments, and validation strategies for new ...
Experience with commissioning, qualification, and validation (CQV) * Background in semiconductor, pharmaceutical, biotech, or similar industries * Lean construction experience (Last Planner System ...
Experience with commissioning, qualification, and validation (CQV) * Background in semiconductor, pharmaceutical, biotech, or similar industries * Lean construction experience (Last Planner System ...
Experience with commissioning, qualification, and validation (CQV) * Background in semiconductor, pharmaceutical, biotech, or similar industries * Lean construction experience (Last Planner System ...
Experience with commissioning, qualification, and validation (CQV) * Background in semiconductor, pharmaceutical, biotech, or similar industries * Lean construction experience (Last Planner System ...
... biotech, or medical device environments, particularly in GMP and ISO quality contexts. * Exposure to quality engineering practices related to equipment lifecycle, calibration, and validation.
Quick apply
... biotech, or medical device environments, particularly in GMP and ISO quality contexts. * Exposure to quality engineering practices related to equipment lifecycle, calibration, and validation.
Virginia, MN · On-site
... biotechnology environments. * Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV). Technical Skills: * Exposure to MES platforms such as Tempo, Syncade, or ...
New
Virginia, MN · On-site
... biotechnology environments. * Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV). Technical Skills: * Exposure to MES platforms such as Tempo, Syncade, or ...
New
Plymouth, MN · On-site
$25 - $29.50/hr
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
Quick apply
Plymouth, MN · On-site
$25 - $29.50/hr
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
... biotech, or medical device environments, particularly in GMP and ISO quality contexts. * Exposure to quality engineering practices related to equipment lifecycle, calibration, and validation.
Quick apply
... biotech, or medical device environments, particularly in GMP and ISO quality contexts. * Exposure to quality engineering practices related to equipment lifecycle, calibration, and validation.
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
Plymouth, MN · On-site
$25 - $29.50/hr
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
Plymouth, MN · On-site
$25 - $29.50/hr
... validation of your expertise and technical competency. This role offers unmatched exposure across the biotech, med-tech, pharmaceutical, and healthcare sectors. You'll perform certification ...
... and biotechnology? At Molecular Devices, one of Danaher's 15+ operating companies, our work saves ... Must have a valid driver's license with an acceptable driving record It would be a plus if you also ...
... and biotechnology? At Molecular Devices, one of Danaher's 15+ operating companies, our work saves ... Must have a valid driver's license with an acceptable driving record It would be a plus if you also ...
... and biotechnology? At Molecular Devices, one of Danaher's15+ operating companies, our work saves ... Must have a valid driver's license with an acceptable driving record It would be a plus if you also ...
... and biotechnology? At Molecular Devices, one of Danaher's15+ operating companies, our work saves ... Must have a valid driver's license with an acceptable driving record It would be a plus if you also ...
Maple Grove, MN · On-site
... Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our ... Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V ...
Maple Grove, MN · On-site
... Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our ... Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V ...
Saint Paul, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Saint Paul, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Moundsview, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Moundsview, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Moundsview, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Moundsview, MN · On-site
$86K - $160K/yr
Knowledge of PLCs, HMI/SCADA, VFDs, P&IDs, Good Manufacturing Practices, and validation workflows within the pharmaceutical/biotech industries is fundamental to this role. This position works closely ...
Experience (last 5 years) in pharmaceutical/biotech/healthcare or similarly structured complex ... Reside within territory or within 50 miles of the territory border; travel 60-80%; valid driver ...
Experience (last 5 years) in pharmaceutical/biotech/healthcare or similarly structured complex ... Reside within territory or within 50 miles of the territory border; travel 60-80%; valid driver ...
Minneapolis, MN · On-site
... biotechnology, and medical device roles. I came across your profile and wanted to see if you are ... Collaborate with Engineering, Manufacturing, Validation, and Operations teams during project ...
Quick apply
Minneapolis, MN · On-site
... biotechnology, and medical device roles. I came across your profile and wanted to see if you are ... Collaborate with Engineering, Manufacturing, Validation, and Operations teams during project ...
For Biotech Validation jobs in Minnesota, the most frequently searched job titles are:
The top searched job categories for Biotech Validation jobs in Minnesota are:
Cities in Minnesota with the most Biotech Validation job openings:
Maple Grove, MN • On-site
Other
Posted 2 days ago
New
Maple Grove, United States | Posted on 05/11/2026
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Job DescriptionJob Role : Senior Design Assurance Engineer — Medical Device (Onsite — Arbor Lakes , MN ) Contract
Overview:
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Our F500 Medical Device client has an exciting opportunity for a Senior Design Assurance Engineer.
Job Summary:
The Sr Design Assurance Engineer provides focused quality engineering leadership on sustaining design assurance activities. Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V) process. This includes quality plans, risk management plans and reports, hazard analysis, product risk management workbook (user FMEA and design FMEA), sampling systems / procedures and statistical techniques, verification protocols/testing/reports, validation protocols/testing/reports. This role will be responsible for supporting risk document and post market record review during remediation activities as well as ensuring quality and compliance through post commercialization sustaining activities.
RequirementsRequired Qualifications
Preferred Qualifications:
Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.
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It services
11 - 50 Employees
Fort Lauderdale, FL, US
2013
