| Job alert | Jobs 11 - 20 of 210 |
Senior Laser Process Engineer
Integer Holdings Corporation
–
Chaska, MN, 55318
... Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. You will develop new and unique approaches to complex problems and lead projects to advance Integer’s technological ... - Apr 29
Analyst, Product Surveillance
SMS Staffing Inc.
–
Plymouth, MN
... Completing FDA MDR (Medical Device Reporting) and other outside competent authority regulatory reports. Will work in the lab, assisting with returned product root cause investigations and evaluation submissions. May also be tasked with assisting in ... - May 16
Product Surveillance Analyst
Talentrupt RPO
–
Plymouth, MN, 55442
... Complete FDA MDR and other outside competent authority regulatory reports. - May 16
Maintenance Technician - 3rd Shift
QualiTech
–
Chaska, MN, 55318
... software (FIIX, MP2 etc.) Embrace business and personal continuous improvement initiatives Experience in manufacturing environment Experience in a FDA regulated environment Compensation details: 30-38 Hourly Wage PI0c4b883fba8a-2625 Permanent - May 02
Entry Level Laboratory Technician
Actalent
–
Chaska, MN, 55318
... on solutions which include pH, conductivity, and density, to ensure adherence to production/process specifications -Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. ... - May 15
Director of Quality Assurance
DDL, Inc.
–
Eden Prairie, MN, 55344
... 15+ years of QA experience in the pharmaceutical industry or a combination of pharmaceutical and other related FDA/EU regulated industry. 10+ years’ experience managing a team. 5+ years of Regulatory Affairs experience. Microsoft Office software ... - May 13
Maintenance Technician - 3rd Shift
QualiTech, Inc.
–
Chaska, MN, 55318
... MS Office knowledge * Knowledge of maintenance and asset management software (FIIX, MP2 etc.) * Embrace business and personal continuous improvement initiatives * Experience in manufacturing environment * Experience in a FDA regulated environment - May 07
Lab Technician - Medical Diagnostics
Actalent
–
Chaska, MN, 55318
... on solutions which include pH, conductivity, and density, to ensure adherence to production/process specifications -Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. ... - May 15
Analyst, Product Surveillance
SMS Staffing Inc.
–
Plymouth, MN, 55442
... * Completing FDA MDR (Medical Device Reporting) and other outside competent authority regulatory reports. * Will work in the lab, assisting with returned product root cause investigations and evaluation submissions. * May also be tasked with ... - May 17
Quality Assurance Supervisor
Federal Package Network, Inc.
–
Chanhassen, MN, 55317
... Working knowledge of FDA regulations and GMPs. Self-directed with strong organizational skills and attention to detail. Proficient in communication, report writing, and grammar. Strong aptitude for critical thinking. Capable of making confident ... - May 10