Quality Engineer (Hybrid - Eagan, MN)

We need to output HTML fragment with sections: headings

for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections with real content. No job title heading. No Job ID. Remove boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning, duplicated lines, application instructions. Keep substantive info. We need to parse the posting. Content: - Intro paragraph about Solventum: "At Solventum, we improve lives by helping healthcare professionals do their best work. Join a team using innovation and insight to make a real impact on the future of healthcare." Then "All roles listed are with Solventum, and we’re committed to protecting your personal information—learn more in our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/" - Then "Job Description Quality Engineer 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you." - Then "The Impact You’ll Make in this Role As a Quality Engineer You Will Have The Opportunity To Tap Into Your Curiosity And Collaborate With Some Of The Most Innovative And Diverse People Around The World. Here, You Will Make An Impact By Supporting marketed medical device and drug products by managing changes, handling complaints, conducting CAPA, leading risk management, performing design validation, developing and validating physical and analytical test methods, and ensuring compliance with our QMS and global medical device and drug product regulations. Reviewing batch records for drug product release, investigating, escalating, and resolving nonconformances and deviations. Collaborating with internal cross-functional team members and external suppliers to ensure performance. Preparing for and participating in government inspections, and customer, notified body, and internal audits." - Then "Your Skills And Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications: Bachelor’s Degree or higher AND seven (7) years of experience in combined product, quality, engineering, and/or laboratory/technical experience in a private, public, government or military environment AND In addition to the above requirements, the following are also required: Three (3) years of experience in the drug, pharmaceutical, and/or medical device industry Additional qualifications that could help you succeed even further in this role include: Experience leading and collaborating on cross-functional projects. Experience applying statistical and quality engineering tools, such as Gage R&R, ANOVA, FMEA, SPC, process capability analysis, regression analysis, and design of experiments (DOE). Experience working in an engineering, analytical chemistry, or other laboratory-based technical role. Experience analyzing technical, quality, manufacturing, and/or product-related issues and supporting risk-based decisions. Experience managing multiple priorities, projects, or initiatives and achieving established objectives. Experience communicating technical information to stakeholders through verbal discussions, presentations, and written communications. Experience leading process improvement initiatives." - Then "Work location: Hybrid Eligible (Job Duties allow for some remote work but require travel to Eagan, MN) Travel: May include up to 20% domestic/international Relocation Assistance: May be authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status)." - Then "Supporting Your Well-being Solventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only: The expected compensation range for this position is $106,000 - $145,750, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-Rewards" - Then "Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties." - Then a bunch of boilerplate about fraud, EEO, etc. We need to remove those. We need sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what content goes where. - About the role: Could be the intro describing Solventum and the role impact. Possibly combine the first paragraphs about Solventum and the impact. - Responsibilities: The bullet list of duties: supporting marketed medical device and drug products by managing changes, handling complaints, conducting CAPA, leading risk management, performing design validation, developing and validating physical and analytical test methods, ensuring compliance with QMS and global regulations, reviewing batch records, investigating/escalating/resolving nonconformances and deviations, collaborating with internal cross-functional team members and external suppliers, preparing for and participating in government inspections, customer, notified body, and internal audits. Also "Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties." That's a responsibility. - Requirements: Minimum qualifications: Bachelor’s Degree or higher AND seven (7) years of experience in combined product, quality, engineering, and/or laboratory/technical experience in a private, public, government or military environment AND three (3) years of experience in the drug, pharmaceutical, and/or medical device industry. - Qualifications: Might be same as Requirements? Usually "Qualifications" includes required and preferred. But we have "Additional qualifications that could help you succeed even further in this role include:" list of experiences. That could go under Qualifications (preferred) or Skills. The instruction: Use headings for Requirements, Qualifications, Skills. We need to decide distribution. We have "Your Skills And Expertise" heading in original. That includes required qualifications and additional qualifications. So we could treat that as Skills section. But we also have explicit "Requirements" (minimum). So we can have Requirements (minimum) and Qualifications (preferred) and Skills (maybe tools). However the instruction says prefer a few substantive sections over many thin ones. So we might combine. We need to include Pay and Benefits sections if posting actually states them. It does: compensation range and benefits list. So we need Pay and Benefits sections. Schedule: The posting mentions work location hybrid, travel up to 20%, relocation assistance. That's not exactly schedule but could be considered schedule? The instruction says include Schedule section only if posting actually states them. It does not explicitly state schedule like full-time, part-time, shift. It mentions hybrid eligible, travel. Could be considered schedule? Might be better to not create Schedule section if no explicit schedule info. The instruction: "never create Pay/Schedule/Benefits sections unless the posting actually states them." It does state work location hybrid, travel, relocation. That's not schedule but maybe considered schedule? I'd argue schedule refers to work hours, shift, etc. Not present. So omit Schedule. Thus sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay. But we might combine Requirements and Qualifications into one? However we have distinct content: minimum qualifications (Bachelors + 7 years + 3 years industry) and additional qualifications (experience leading cross-functional projects, statistical tools, etc.). Could put both under Requirements (maybe split into Required and Preferred). But we have separate headings allowed. Let's do Requirements for minimum, Qualifications for additional preferred, Skills for tools and expertise? However the "Your Skills And Expertise" includes both required and additional. Might be redundant. Better: Use sections: About the role, Responsibilities, Requirements (minimum), Qualifications (preferred), Skills (tools/expertise), Benefits, Pay. Check if any content duplicates. Let's extract: About the role: Combine introductory paragraphs about Solventum and the role impact. Paragraph 1: "At Solventum, we improve lives by helping healthcare professionals do their best work. Join a team using innovation and insight to make a real impact on the future of healthcare. All roles listed are with Solventum, and we’re committed to protecting your personal information—learn more in our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/" Paragraph 2: "Job Description Quality Engineer 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you." Paragraph 3: "The Impact You’ll Make in this Role As a Quality Engineer You Will Have The Opportunity To Tap Into Your Curiosity And Collaborate With Some Of The Most Innovative And Diverse People Around The World. Here, You Will Make An Impact By Supporting marketed medical device and drug products by managing changes, handling complaints, conducting CAPA, leading risk management, performing design validation, developing and validating physical and analytical test methods, and ensuring compliance with our QMS and global medical device and drug product regulations. Reviewing batch records for drug product release, investigating, escalating, and resolving nonconformances and deviations. Collaborating with internal cross-functional team members and external suppliers to ensure performance. Preparing for and participating in government inspections, and customer, notified body, and internal audits." We could keep that as About the role. Responsibilities: Could be the list of duties (the same as impact). But we already used that. Maybe separate: Responsibilities: list of duties (managing changes, handling complaints, CAPA, risk management, design validation, developing/validating test methods, ensuring compliance, reviewing batch records, investigating/escalating/resolving nonconformances, collaborating with internal/external, preparing for inspections/audits). Also "Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties." We'll put that in Responsibilities. Requirements: Minimum qualifications: Bachelor’s Degree or higher AND seven (7) years of experience in combined product, quality, engineering, and/or laboratory/technical experience in a private, public, government or military environment AND three (3) years of experience in the drug, pharmaceutical, and/or medical device industry. Qualifications: Additional qualifications that could help you succeed even further: Experience leading and collaborating on cross-functional projects. Experience applying statistical and quality engineering tools, such as Gage R&R, ANOVA, FMEA, SPC, process capability analysis, regression analysis, and design of experiments (DOE). Experience working in an engineering, analytical chemistry, or other laboratory-based technical role. Experience analyzing technical, quality, manufacturing, and/or product-related issues and supporting risk-based decisions. Experience managing multiple priorities, projects, or initiatives and achieving established objectives. Experience communicating technical information to stakeholders through verbal discussions