Strong FDA 21 CFR 820 and ISO 13485 knowledge * 5+ years of Leadership experience Quality Control ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Strong FDA 21 CFR 820 and ISO 13485 knowledge * 5+ years of Leadership experience Quality Control ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Sr. R&D Engineer
Eden Prairie, MN · On-site
$100K - $120K/yr
Ensure compliance with regulatory and industry standards (FDA, MDD/MDR, ISO, ASTM, etc.) as ... May mentor or supervise less experienced engineers, interns, and co-ops. * Other duties as ...
Quick apply
Sr. R&D Engineer
Eden Prairie, MN · On-site
$100K - $120K/yr
Ensure compliance with regulatory and industry standards (FDA, MDD/MDR, ISO, ASTM, etc.) as ... May mentor or supervise less experienced engineers, interns, and co-ops. * Other duties as ...
Program Manager
Dassel, MN · On-site
$100K - $151K/yr
Knowledge of ISO 13485, and FDA regulations * Complete understanding of MRP and DFM principles ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Program Manager
Dassel, MN · On-site
$100K - $151K/yr
Knowledge of ISO 13485, and FDA regulations * Complete understanding of MRP and DFM principles ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Quality Control Manager
Brooklyn Park, MN · On-site
$100K - $151K/yr
Strong FDA 21 CFR 820 and ISO 13485 knowledge * 5+ years of Leadership experience Quality Control ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Quality Control Manager
Brooklyn Park, MN · On-site
$100K - $151K/yr
Strong FDA 21 CFR 820 and ISO 13485 knowledge * 5+ years of Leadership experience Quality Control ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Apply GLP and GCP guidelines for FDA and regulatory submissions. * Contribute to drafting and ... Train and mentor less experienced CIC staff, veterinary students, interns, and residents. * Provide ...
Apply GLP and GCP guidelines for FDA and regulatory submissions. * Contribute to drafting and ... Train and mentor less experienced CIC staff, veterinary students, interns, and residents. * Provide ...
Software Verification Engineer I - 2 Openings
Saint Paul, MN · On-site
$33 - $35/hr
... FDA regulatory,and ISO standard procedures. * Design new test suites for new features and ... Experience working on academic or internship projects involving testing or product development.
Quick apply
Software Verification Engineer I - 2 Openings
Saint Paul, MN · On-site
$33 - $35/hr
... FDA regulatory,and ISO standard procedures. * Design new test suites for new features and ... Experience working on academic or internship projects involving testing or product development.
Production Operator Assembler I - 1st shift
Dassel, MN · On-site
$18 - $22/hr
Familiarity with FDA, ISO, cGMP, Lean manufacturing, or workplace safety practices. * Experience ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Production Operator Assembler I - 1st shift
Dassel, MN · On-site
$18 - $22/hr
Familiarity with FDA, ISO, cGMP, Lean manufacturing, or workplace safety practices. * Experience ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Cell Lead I - 2nd shift
Dassel, MN · On-site
$23 - $30/hr
Familiar with ISO and FDA requirements * Certifications in a related field What is it like to work ... tell potential interns that Cretex is a great company to work for. It has set a high bar for ...
Fda Internship information
See Minnesota salary details
$8.48 - $9.65
2% of jobs
$9.65 - $10.83
4% of jobs
$10.83 - $12.01
14% of jobs
$12.46 is the 25th percentile. Wages below this are outliers.
$12.01 - $13.18
12% of jobs
$13.18 - $14.36
15% of jobs
The median wage is $14.53 / hr.
$14.36 - $15.54
18% of jobs
$16.68 is the 75th percentile. Wages above this are outliers.
$15.54 - $16.72
10% of jobs
$16.72 - $17.89
6% of jobs
$17.89 - $19.07
8% of jobs
$19.07 - $20.25
5% of jobs
$20.25 - $21.42
5% of jobs
$8
$15
$21
How much do fda internship jobs pay per hour?
What is an FDA internship?
An FDA Internship is a temporary position designed for students or recent graduates to gain hands-on experience in regulatory science, public health, and policy. Interns work on projects related to drug approval, food safety, medical devices, and other areas overseen by the U.S. Food and Drug Administration. These internships provide valuable exposure to federal regulations, research, and compliance processes. Opportunities may be available in various FDA offices and centers, offering mentorship and professional development.
What kinds of projects or tasks do FDA interns typically work on during their internship?
FDA interns often work on a variety of projects related to public health, regulatory policy, scientific research, or data analysis, depending on their department. Interns may assist with laboratory studies, analyze clinical trial or adverse event data, contribute to policy reviews, or help draft scientific reports and communications. Supervision and mentorship are typically provided by experienced professionals, and interns often have opportunities to attend seminars or networking events. This hands-on experience provides valuable practical insight into the federal regulatory process and helps interns build skills for future careers in science or public health.
What are the key skills and qualifications needed to thrive in the FDA internship position, and why are they important?
To thrive as an FDA Intern, you generally need a background in life sciences, public health, pharmacy, or a related field, along with strong analytical and research skills. Familiarity with data analysis tools, laboratory techniques, or regulatory databases is often beneficial depending on the specific internship focus. Excellent written and verbal communication, attention to detail, and the ability to work collaboratively in multidisciplinary teams are stand-out soft skills. These attributes are crucial for meeting the FDA's standards for study integrity, regulatory compliance, and effective information sharing within complex projects.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 4 days ago
Job description
About Cretex Medical:
Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at www.cretexmedical.com.
Quality Control Manager Position Summary:
The Quality Control Manager (QC Operations) leads Incoming Inspection, In-Process Inspection, Final Inspection, and Quality Laboratory functions while partnering closely with New Product Development (NPD/NPI) and Manufacturing to ensure compliant product realization and operational excellence. This role drives risk-based quality control strategies, regulatory compliance, and continuous improvement to deliver high-quality products right the first time. The role requires a hands-on technical leader who can set direction, prioritize workload, coach and develop the team, and effectively interface with plant leadership and cross-functional stakeholders.
ResponsibilitiesLeadership & Team Management- Lead, coach, and develop Inspection and Quality Control teams across Incoming, In-Process, and Final Inspection, as well as Quality Laboratory functions.
- Establish and manage Inspection & QC objectives and KPIs aligned with site quality, safety, delivery, and cost targets.
- Build a high-performance culture focused on compliance, defect prevention, continuous improvement, and accountability.
- Drive workforce planning and resource allocation to support production demand, new product introductions (NPI), and engineering changes.
- Ensure inspector training, certification, and qualification meet regulatory and technical requirements.
Measurement Process Ownership
- Own the end-to-end inspection and quality control lifecycle, from requirements definition through validation, release, and controlled change for production use.
- Establish and maintain standardized work for inspection methods, sampling plans, documentation, and change control within the Quality Management System
- Ensure inspection processes are robust, efficient, and capable, delivering accurate, repeatable, and reliable results.
- Define and govern inspection strategies, including visual, dimensional, functional, and test methods, aligned with engineering requirements and risk-based quality principles.
- Drive standardization of inspection approaches across parts, processes, shifts, and sites to reduce variation, rework, and release cycle time.
Continuous Improvement & Compliance
- Lead initiatives to improve first-time-right quality, reduce cycle time inspection, and lower the cost of poor quality.
- Ensure adherence to regulatory requirements, internal procedures, & customer standards for inspection & product release
- Maintain compliant documentation, including inspection records, DHRs, validation evidence, and controlled procedures.
- Incorporate lessons learned from nonconformances, escapes, and audits into updated inspection methods and controls.
- Apply data-driven tools such as SPC, trend analysis, and risk-based sampling to drive proactive quality improvement.
Stakeholder Management & Communication
- Partner with Design, Operations, Engineering, and Quality to align inspection strategy with manufacturing execution.
- Communicate performance trends, risks, and improvement actions clearly to site leadership.
- Support NPI readiness and engineering changes through inspection planning and execution.
- Represent Inspection & Quality Control in cross-functional reviews and audits.
Quality Control Manager Requirements:
- Bachelor's degree in engineering, or related field
- 5+ years in Quality Control or Manufacturing Quality
- Strong FDA 21 CFR 820 and ISO 13485 knowledge
- 5+ years of Leadership experience
Quality Control Manager Preferred Requirements:
- Lean/Six Sigma experience
- High-mix manufacturing environment experience
- Strong data and problem-solving skills
What is it like to work at Cretex Medical?
We recognize the contribution of every individual and promote growth, safety and security for all our employees. Cretex Medical values performance and pays competitive wages along with a rich benefit package. We offer a positive work environment with a focus on continuous improvement.
Here are some of things that employees have said about working for Cretex Medical:
- "The culture at Cretex is collaborative. Everyone here is willing to help you whether it is a director, a machinist, or your boss. Everyone is always willing to help you figure out a project and get it done right."
- "I would tell potential interns that Cretex is a great company to work for. It has set a high bar for corporate culture as well as the quality of work you can do. I would definitely recommend it."
- "I learned that I really like the medical device industry. The importance and the gravity of what we do here is felt by the employees. You can have that passion in your work because you know what you are striving for is to save lives."
We encourage you to explore the many opportunities Cretex Medical can offer you as a valued team member.
#LI-JW1
Pay RangeUSD $100,900.00 - USD $151,300.00 /Yr.Pay Range DetailsThis pay range reflects the base hourly rate or annual salary for positions within this job grade, based on our market-based pay structures. Actual compensation will depend on factors such as skills, relevant experience, education, internal equity, business needs, and local market conditions. While the full hiring range is shared for transparency, offers are rarely made at the minimum or maximum of the range.
Company BenefitsCompensation:
This is a bonus eligible postion.
All Employees:
Our 401k retirement savings plan with a company match contribution; onsite health clinics, discretionary holiday bonus program (based on years of service), Cretex University, 24/7 employee assistance program with access to five confidential visits with a licensed counselor at no cost, wellness program with incentives, an employee death benefit, and employee sick and safe leave are available to all Cretex employees.
20+hours:
Cretex's medical benefit package includes: comprehensive medical insurance with access to virtual providers; dental insurance (Little Partners Dental benefit covers services 100 percent for children 12 and younger when seen by a Health Partners in network provider); vision insurance; a pre-tax health savings account, healthcare and dependent care pre-tax reimbursement accounts; paid holidays, paid time off; and our discretionary profit sharing program are available to employees working 20+ hours/week.
30+ hours:
Parental Leave, accident and critical illness benefits, optional employee, spouse, and child life; short and long term disability; company provided life insurance; and tuition assistance programs are available to employees working 30+ hours per week.
(Some benefits are subject to eligibility criteria.)
Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law.
Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
Employment Type: FULL_TIME