Phoenix, AZ · On-site +1
$143K - $238K/yr
Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree ... Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in ...
Phoenix, AZ · On-site +1
$143K - $238K/yr
Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree ... Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in ...
$10.98 - $18.46
3% of jobs
$18.46 - $25.94
11% of jobs
$30.08 is the 25th percentile. Wages below this are outliers.
$25.94 - $33.42
20% of jobs
The median wage is $38.76 / hr.
$33.42 - $40.90
22% of jobs
$40.90 - $48.38
14% of jobs
$52.12 is the 75th percentile. Wages above this are outliers.
$48.38 - $55.86
10% of jobs
$55.86 - $63.34
7% of jobs
$63.34 - $70.82
4% of jobs
$70.82 - $78.30
3% of jobs
$78.30 - $85.77
3% of jobs
$85.77 - $93.25
2% of jobs
$10
$46
$93
A Stryker RN is a registered nurse who works for Stryker, a medical technology company specializing in healthcare solutions. These nurses typically focus on clinical support, training, and education for healthcare professionals using Stryker's medical devices. They may assist in operating rooms, provide product demonstrations, and ensure proper usage of Stryker equipment to improve patient outcomes. This role combines nursing expertise with technical knowledge to enhance patient care and hospital efficiency.
As a Stryker RN, your daily responsibilities often include providing clinical education on Stryker medical devices, supporting surgical teams during procedures, and troubleshooting equipment in real time. You'll collaborate closely with surgeons, nurses, and hospital staff to ensure devices are used safely and effectively, and may also participate in in-servicing and training sessions. In addition to maintaining up-to-date knowledge of the latest technologies, you'll help bridge communication between Stryker representatives and healthcare facilities. This hands-on, dynamic role offers the chance to develop advanced technical skills and play a key part in enhancing patient care outcomes.
To thrive as a Stryker RN, you need a current registered nurse (RN) license, strong clinical skills, and a solid understanding of surgical or medical equipment, typically within an orthopedic or surgical setting. Familiarity with Stryker products, medical device protocols, and possibly specialized certifications such as Basic Life Support (BLS) or Advanced Cardiovascular Life Support (ACLS) are often required. Exceptional communication, problem-solving abilities, and adaptability are key soft skills for educating staff, supporting surgical teams, and handling high-pressure situations. These competencies are critical for ensuring optimal patient outcomes, effective team collaboration, and the safe use of complex medical devices in fast-paced healthcare environments.
The most popular types of Stryker Rn jobs in Phoenix, AZ are:
For Stryker Rn jobs in Phoenix, AZ, the most frequently searched job titles are:
The top searched job categories for Stryker Rn jobs in Phoenix, AZ are:
$143K - $238K/yr
Full-time
Posted 10 days ago
8.2
Based on 112 frontline employees who took The Breakroom Quiz
130th of 495 rated machine equipment manufacturers
Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.
As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.
What You Will Do
Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.
Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.
Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.
Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.
Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.
Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.
Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.
Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.
What You Need
Required
Bachelor's degree in a scientific, technical, healthcare, or related discipline.
Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.
Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.
Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.
Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.
Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.
Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.
Preferred
Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.
Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.
Experience supporting regulatory submissions and global market access initiatives for medical devices.
Knowledge of clinical operations, risk management, and international regulatory requirements.
United States of America Pay Ranges:
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
10,000+ Employees
Kalamazoo, MI, US
