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Healthmark Industries Co., Inc.
Clinical Affairs Specialist
Career Insights for Compliance Officer / Analyst
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What they do
A Compliance Officer or Analyst monitors internal compliance with company policies and also company compliance with local, state and federal laws. Reviews company documents, including contracts and marketing materials; communicates with employees and develops training and internal policy materials.
$71,678 / year median in the U.S.
-3% projected decline
Job Description
Clinical Affairs Specialist Healthmark Industries Co., Inc.
- 3.5 Fraser, MI Job Details $70,720
- $88,400 a year 12 hours ago Benefits Commuter assistance Caregiver leave Disability insurance Health insurance Dental insurance Flexible spending account Tuition reimbursement Paid time off Parental leave Vision insurance 401(k) matching Life insurance Qualifications Customer communication OR experience Product development E-learning platforms Biomedical regulatory compliance Healthcare infection prevention and control compliance expertise Enterprise Learning Management monday.
Full Job Description Date:
Jul 9, 2026Location:
Fraser, MI, US Company:
Healthmark Industries Co., Inc.Remote Work:
1-2 days at home (site based)Salary Range:
$70,720- $88,400/annually + 4% STIP With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers
- and to save more lives, we need team players, forward thinkers, and game changers.
Job Responsibilities and Essential Duties:
Collaborate with Product Management, Quality, Regulatory, and R D teams throughout the product lifecycle. Assist in development and review of clinical and technical product documentation. Provide logistical support to Clinical Affairs and Commercial Education activities, including planning, scheduling, tracking, and reporting. EDU Inbox Management- Actively monitors and responds to the EDU email inbox, addressing inquiries from sales reps, educators, and internal team members, or routing as appropriate. Healthmark Academy Administration
- Manages the Healthmark Academy inbox, QR code generation, correspondence, flyer development, and reporting. Structural development and maintenance of educational programs. Speaking & Focused Assessment Coordination
- Oversees speaking requests and focused assessment requests, including scheduling and customer/sales correspondence, through Monday.com. Manages and submits all CE programs for approval to the appropriate certification bodies and tracks them within Monday.com. Content Compliance & Audit Oversight
- Audits Monday.com entries to ensure educators are uploading presentations, assessment reports, articles, and related materials for completeness and compliance. KPI Management
- Enters and maintains departmental KPIs in 90.
Required Knowledge, Skills and Abilities:
Associate's or Bachelor's Degree in a related field (nursing, surgical technology, education, etc.) is preferred but not required. Experience as SPD Educator preferred. Additional sterile processing related certifications preferred (CHL, CIS, CER, etc.). Strong understanding of sterile processing workflows, infection prevention principles, and perioperative practices. Ability to support product lifecycle and commercialization activities. Exceptional attention to detail. Excellent communication and presentation skills (written and verbal). Proficient user of Microsoft Office Suite, Adobe Acrobat, Monday.com, LMS platforms, and related administrative systems. Local to Healthmark office in Fraser, Michigan. Would work in the office at least three days a week.Minimum Requirements:
Five years of experience is required (i.e., within a Sterile Processing/Operating Room). Certification as a sterile processing technician (HSPA or CBSPD).Quality Requirements:
Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function). Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function). Attend all required Quality & Compliance training at the specified interval. Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements.Environmental/Safety/Physical Work Conditions:
Sit for long periods of time. Communicate with staff and customers. Stand for long periods of time. Take notes. Travel as needed. Lift up to 25 lbs. Solve problems. The physical demands described here are a representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. $70,720- $88,400/annually + 4% STIP #LI-JF1 #LI-Hybrid About us With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows.