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Medical Device Specialist Jobs in Arkansas

Technical Support Specialist - Medical Device
By R92 At United States
1 -2 year experience in medical device industry background
Proactive and results-oriented who can work independently and as part of a team to effectively manage assignments and support customer queues.
Must have excellent verbal and written communication skills.
Good interpersonal skills with the ability to react quickly, accurately, and remain calm under pressure.
1- 2 years related experience providing technical support
Experience using mobile devices such as cell phone, laptop and tablet to perform work activities
Employee Relations Specialist (Medical Device/Pharma)
By Rangam At United States
Case management and Zendesk exp. would pe preferable but not a requirement
Able to work with Managers and other stakeholders too
Must have ER investigations experience
Looking for 3-5 years of experience
Someone who has working as a HR Manager and having an exp. with Employee relations would be work
Provides expert consultative and problem solving services to managers, employees and other HR functions regarding HR policies and practices.
Director Of Quality - Medical Device
By EPM Scientific At United States
A minimum of 8 years of experience in quality management within the medical device industry, including leadership roles.
Lead a team of quality professionals, including hiring, training, and performance management, to create a culture of excellence and collaboration.
Certified Quality Manager (CQM), Certified Quality Engineer (CQE), or other relevant certifications are a plus.
Lead and manage internal and external quality audits, ensuring compliance with regulatory standards and driving corrective and preventive actions as needed.
Proven track record of leading successful quality teams and managing complex projects in a remote or virtual work environment.
Excellent communication skills, with the ability to collaborate effectively with cross-functional teams and communicate complex quality concepts to diverse audiences.
Medical Device Clinician/Nurse/Doctor
By Infosoft, Inc. At United States
Analyze complex clinical evaluation reports (CER) regulatory submissions, regulatory agency requests, and/or management reports including ad hoc report
Knowledge ofMedical Device regulations, such asFDA 21 CFR 820, ISO 13485; MDD; CMDR EU MDR, and other applicable regulatory requirements.
Provide knowledge transfer and product training for team members
Other incidental duties: Maintain relevant education/training
Excellent facilitation, presentation, and public speaking skills
Full knowledge and understanding of the Client's policies, procedures, and guidelines
Medical Device Clinical Specialist
By nextOPP Search At United States
• Efficient project management and communication capabilities along with strong analytical and strategic thinking skills
• Own budget tracking and milestone management
• Strong presentation experience and proficient PowerPoint skills
*This is a remote role but requires 40-50% travel in the Northeast Region of the US.
• Manage external medical conferences and engage with external customers
• 3+ years of relevant healthcare experience / preferably oncology, NICU, pediatrics, post-op or geriatrics
Medical Device Complaint Reviewer
By The Fountain Group At United States

NURSING DEGREE REQUIRED (BSN or RN or Nurse Practitioner) The Pharmacovigilance and Patient Safety (PPS) organization works collaboratively and strategically with colleagues across the product ...

Remote: Qa Medical Device Contractor (233511)
By Black Diamond Networks At United States
Knowledge of ISO 9001 and ISO 13485
General knowledge of QA and RA compliance for Class I Med Devices
Experience mentoring younger staff is a plus (+)
8-10 Years working in FDA regulated Medical Device Industry
Working with Salesforce and D365 is preferred
Medical Writer - Medical Device
By Integrated Resources, Inc ( IRI ) At United States
Top 3 things the manager is looking for:
Previous PSUR writing experience or experience writing documents relevant to EU MDR
Top 3 Tasks or Responsibilities in Product for this role:
Communicates primarily and frequently with internal contacts. Big picture thinking with problem solving skills
University degree with minimum two years experience. Masters level preferred
Location: Remote - time zone: preferably CST, Eastern or PST
Qa Medical Device Contractor (233511)
By Black Diamond Networks At United States
Knowledge of ISO 9001 and ISO 13485
General knowledge of QA and RA compliance for Class I Med Devices
Experience mentoring younger staff is a plus (+)
8-10 Years working in FDA regulated Medical Device Industry
Working with Salesforce and D365 is preferred
Degree: Not needed but preferred
Regulatory Affairs Specialist - Medical Device
By Integrated Resources, Inc ( IRI ) At United States
Create and manage IVDR Technical Files.
It would be a plus if you also possess previous experience in: 510k author.
Work with international colleagues on establishing design dossiers for their intended market for new product development and design changes.
Subject matter expertise in registration and commercialization of medical devices.
Customer Service Representative (Medical Device)
By Insight Global At United States
- 3+ years of call center experience
- Strong communication skills and a strong aptitude to learn new skills
Customer Service Rep (Inbound Calls)
- Technologically advanced and confident in their ability to walk an individual through technology issues
Write at least 30 words per minute
Qc Analyst (Medical Device/Pharmaceutical)
By Omni Inclusive At United States
Data analysis and problem-solving skills are necessary to identify and countermeasure common failure issues.
Robust documentation and strict adherence to approved procedures are a requirement in the highly regulated work environment.
Evaluate documentation of service records against expected standard across a complex product portfolio.
Initiate remediation of service records and/or generate customer complaints when gaps are revealed.
Utilize MS Excel analytics to provide service leadership with reporting as well as trending of failures including recommendations for improvement.
Communicate with Customer Technical Specialists, Field Service & Application Engineers to gather more data when needed.
Program Manager - Medical Device
By Integrated Resources, Inc ( IRI ) At United States
EU MDR Program Management Support
Take on project management remediation process which includes coordinating with program workstream leaders to manage 1 Class II/III Submissions
Identification and timely escalation of project risks to management
Assist in the following activities under the direction of the Program Director:
Develop a robust timeline and plan for the overall program.
Development or improvement of program processes to drive program efficiency
Senior Clinical Research Associate (Medical Device)
By ICON Strategic Solutions At United States

Ability to independently oversee sites and handle not only monitoring responsibility but also oversee site management activities

Ability to travel approximately 30% of the time nationwide

Sales And Marketing Specialist (Medical Device)
By MEL HEALTH TECH CENTER At United States

Sales manager with a flexible schedule for remote and independent work.

Excellent verbal and written communication skills. 2-3 years experience in sales

Medical Device Marketing Manager
By VIVA USA Inc. At United States
Professional certification preferred: Project Management Professional (PMP), Six Sigma, Certified ScrumMaster (CSM), Lean
Key Responsibilities Include (but Are Not Limited To)
Analytic skills: A hands-on, detail-oriented professional with excellent technical, analytical, planning, evaluation and implementation skills.
Clear and effective communication and presentation skills
Experience with Salesforce, Marketo, Excel, Google Analytics, Allocadia, Smartsheet, Microsoft Teams, and Workfront
Prior agency experience, or working with agency vendors
Project Coordinator (Medical Device)
By Select Source International At United States
• 4 years of administrative/project support experience
5+ years of work experience as a project coordinator/administrative assistant
• Capable of working on multiple projects in a deadline driven environment - demonstrated skill under pressure
• Excellent written and verbal communication, and interpersonal skills
• Strong prioritization and organizational skills
• High School Diploma or equivalent
Project Manager- Medical Device
By Integrated Resources, Inc ( IRI ) At United States
Project Management certification (PMP) preferred
Applied knowledge of FDA and international medical device regulations or experience with other highly regulated industry.
Experience with software only medical device
Assign tasks, responsibilities, and accountability to team members to achieve Project and Product goals.
Manage labor, expense, and capital expenditures to multi-million dollar project budgets.
Strong interpersonal skills with ability to promote team interaction and execution
Event Planner (Pharma/Medical Device)
By Rangam At United States
Must have good communication skill
Looking for 1+ year of experience
Must have a general people skill
Bachelor's degree is preferred but it's not a hard requirement
This is a Remote role
Must have exp. with MS Office (Excel is preferred)
Senior Manager - Medical Device
By QuantumBricks At United States

Job Title: Senior Manager - Medical Device Loc: Remote Exp: 10+ Yrs Job Description Mandatory Skill set - Medical Device experience as R&D engineer We are now inviting applications ...