Communicate with the manager about compliance issues or if a negative trend is identified
Hosting customer audits and regulator inspections for the site
Leading internal audits
Support reporting and system use/training as needed
Process document changes in an efficient and timely manner
Ensure accuracy and completeness of documents
Ensure documents accessible through the controlled document management system
Ensure document controls in place for technical accuracy and review
Follow global and Business processes and procedures
Interpreting regulations and representing the customer to foster a quality culture and mindset throughout the plant.
Your skills and expertise
These are the core capabilities and experiences essential to make an impact:
Required Qualifications
Bachelor of Science degree (completed and verified prior to start) from an accredited institution AND 5 years of experience in Quality Management Systems (QMS) or equivalent regulated environment.
OR
High School Diploma/GED from AND 8 years of Quality Management Systems (QMS) experience
Nice to Have” Qualifications
ISO 13485, ISO 9001, and/or pharmaceutical audit and inspection experience· ISO 13485 Lead Auditor Certification· Technical writing skills· CAPA writing and coaching experience
Work Location: Onsite: Maryland Heights, Missouri Location
Travel: May include up to 10% travel within sales territory
Relocation Assistance: May be authorized
Pay Transparency
Applicable to US Applicants Only: The base salary range for this position is $90,000.00 to $110,000.00 with additional bonus opportunities based on performance. 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
Legal & Compliance
Must be legally authorized to work in the country of employment without sponsorship for employment visa status.
Where this role fits
This role sits within Solventum’s Medical Surgical Division, supporting the Acera product portfolio and its clinically proven solutions designed to improve patient outcomes and surgical efficiency. Through Acera Surgical and the Restrata product, the team advances evidence‑based wound care technologies that support healing across multiple surgical specialties, helping frontline healthcare providers deliver safer, more effective care.
Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.
Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of @solventum.com. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.
Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
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