Senior Medical Writer, Clinical Evaluation (Med Devices)
Abbott Laboratories
Abbott Laboratories in Maple Grove MN seeks a Senior Medical Writer, Clinical Evaluation to provide technical and strategic writing across the product life cycle. You will author CER/CEP and PMS/PMCF documents for Neuromodulation, CAHF and Vascular products. You will evaluate clinical evidence from studies, literature, and surveillance, and collaborate with regulatory, quality, and R&D teams to ensure compliant submissions and risk management. #J-18808-Ljbffr Abbott Laboratories
$78k - $156k
...with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115... ..., CA currently has an on-site opportunity for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation...SeniorWork experience placement- ...Job Title: Medical Writer Client: Medical Device Manufacturing Company Duration: 12 Months Location: Maple Grove, MN, 55311 **Mandatory... ...Card Holder Only Key Words: CER (Clinical Evaluation Review/Report) Writing MDR (Medical Device...SuggestedContract workInterim roleFreelance
- ...Medical Writer II We believe that great healthcare is an essential... ...development and execution of clinical, scientific, and regulatory... ...plans and reports, clinical evaluation plans and reports, reports and... ...the support of appropriate device claims, indications, publications...SuggestedFlexible hoursShift work
- ...site) Position Summary The Senior Clinical Engineer role will be responsible... ..., working to study device performance and make recommendations... ..., bench and clinical data. Evaluation of case imaging (fluoroscopy... ...engineering for class III medical devices. Structural heart...SeniorPermanent employmentFull time
- A leading medical device company is seeking a Principal R&D Engineer to drive product development from concept to commercialization. In this role, you will lead cross-functional teams, mentor engineers, and manage multiple projects while ensuring compliance with quality...Suggested
$81k
...US-MN-Maple Grove About the role The Senior Clinical Quality Assurance Specialist assists the... .... Document audit observations, evaluate the impact of audit findings, assess responses... ...(GCP). Auditing experience in the medical device or pharmaceutical industry in an area...SeniorWork at officeLocal areaWorldwide3 days per week- A global medical technology leader is seeking a Principal Regulatory Affairs Specialist in Maple Grove, MN. In this role, you will review... ...of advertising and promotional materials for medical devices. The position requires a minimum of 5 years in regulatory affairs...3 days per week
- VDyne is looking for a Senior Clinical Engineer in Maple Grove, MN to improve and optimize the Transcatheter Tricuspid Valve Replacement therapy. The role involves investigating device performance and collaborating with clinical and R&D teams to analyze outcomes. The ideal...Senior
$102k - $162k
...Senior Clinical Research Associate Job Description The Senior Clinical Research Associate is... ...and minimize impact on study outcomes. Evaluates site performance and capabilities... ...Clinical Research within FDA regulated medical device/product environments, with strong knowledge...SeniorRemote workWork visa$55k - $75k
...HCM is looking for a detail-oriented Quality Inspector to ensure precision-manufactured components meet quality standards in the medical device sector. In this role, you will carry out both in-process and final inspections using calibrated equipment and maintain...Senior- ...technology company is seeking a Senior Operations Manager in Plymouth,... ...8-12 years of operations experience, emphasizing leadership in medical devices. If you're a strategic thinker and team builder, join us to advance life-improving technologies. #J-18808-Ljbffr ENvue MedSenior
- A prominent staffing firm is looking for a Senior Quality Design Engineer in Maple Grove, MN. This role ensures product designs meet... ...minimum of 5 years' experience in design assurance within the medical device industry. Competitive salary range is offered, along with...Senior
- Teleflex is seeking a Senior Clinical Marketing Manager (Remote) to lead clinical content and education programs across coronary/peripheral segments. Responsibilities include developing and deploying the company's clinical marketing strategy, building KOL relationships,...SeniorRemote job
- ...leader to drive the design and development of advanced catheter-based devices within its Cardio & Vascular OEM and Contract Design businesses. The role leads end-to-end product design, translating clinical needs into use requirements, design inputs, and simulated use...SeniorContract work
- Randstad USA is seeking a Technical Writer/Editor/Proofer for labeling and IFU documentation. You will author, edit, translate, and maintain technical documents across the product lifecycle, ensuring accuracy and regulatory compliance. Collaborate with engineering, regulatory...
- Boston Scientific is seeking a Senior Clinical Quality Assurance Specialist to support the Manager, Clinical QA, in maintaining the internal quality assurance program. You will serve as the Clinical QA representative on project teams and conduct audits to ensure compliance...SeniorWork at officeLocal area3 days per week
- ...compliance with regulatory standards. Candidates should have a Bachelor's Degree in life sciences and significant experience in medical device development. Benefits include health care plans, retirement matching, and a commitment to diversity in hiring. #J-18808-Ljbffr...Senior
- ...Affairs Principal to review and approve advertising, promotional, sales support and training materials for interventional cardiology devices. The role applies a risk-based regulatory mindset to ensure accuracy, balance, substantiation and regulatory alignment. The...SeniorWork at office3 days per week
$160k
...Senior Clinical Sales Specialist, Coronary The Senior Clinical Sales Specialist drives clinical adoption of Teleflex coronary complex... ...strongly preferred. ~35+ years of cath lab, clinical, or medical device experience. ~ Prior experience driving product adoption...SeniorTemporary workFlexible hours$20 - $28.85 per hour
...offering the most advanced O&P solutions, clinically differentiated programs and unsurpassed... ...branded and private label O&P devices, products and components, and provides rehabilitative... ...includes Vacation and Sick time ~ Medical, Dental, and Vision Benefits ~401k Savings...Part timeLocal areaRelocation packageFlexible hours$75.1k
...Arden Hills; US-MN-Maple Grove Senior Product Analyst - 12 Month Defined... ...and business operations. Apply clinical knowledge related to product application to evaluate identified complaints.... ...international regulations. Author Medical Device Reports (MDRs), MedWatch reports...SeniorWork at office- TALENT Software Services is seeking a Design Assurance Engineer in Minnesota to support review, update, and maintenance of design control deliverables for the TheraSphere product within the IO&E division. You will work with cross‑functional teams to ensure safety, quality...Senior
$131.2k - $196.8k
...Principal Clinical Evidence Specialist At Medtronic... ...communicating complex medical information to... ...insights to Clinical Evaluation Reports (CERs). A vital... ...Communicates effectively with senior internal stakeholders,... ...) for medical devices, biologics, and/or pharmaceuticals...Work at officeLocal areaFlexible hoursShift work- ...complications. AtriCure's Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib.... ...Room, or hospital setting either through industry or clinical setting preferred, but not required Ability to communicate...SeniorTemporary workWorldwide
- ...expanding surveillance and customer support activities. Using clinical expertise, they will participate in core pharmacology content... ...experience and knowledge of statistics, and research principles when evaluating and interpreting scientific literature and other evidence....SeniorWork at office
$102.1k - $194k
...strategies and prepare submissions for Class II medical devices. Create innovative regulatory pathways... ..., Operations, Medical Safety and Clinical teams. Prepare, coordinate and compile... ...and post‑market activities. Evaluate product and manufacturing changes for regulatory...Work at officeLocal areaOverseas3 days per week$125.8k
...Oncology and Embolization Medical Safety team to ensure... ...product lifecycle. The Senior Manager, Medical Safety... ...and input into Clinical (BSC sponsored clinical... ...unanticipated adverse device effects Represent Medical... ...Scientific continues to evaluate its policies and protocols...SeniorWork at officeLocal area3 days per week$85k
...an exciting opportunity for Senior System Design Quality Engineer... ...of next-generation medical devices International standards compliance... ...-1 and IEC 62304. Uses clinical knowledge to influence how... ...Boston Scientific continues to evaluate its policies and protocols...SeniorHourly payRelocation packageShift work3 days per week$80k - $200k
...experience and a passion for helping customers optimize their Clinical Operations data and document management processes. Veeva’s... ...site selection to study archival, completely adapted for Medical Device, Research Organizations, and Diagnostics Companies of all sizes...SeniorWork at officeLocal areaRemote workWork from homeFlexible hours$102.1k
...functional collaboration with R&D, Medical, and across the marketing... ...drive alignment and execute clinical messaging as a core... ...required 5+ years of Medical Device experience required BA/BS required... ...Boston Scientific continues to evaluate its policies and protocols regarding...SeniorWork at officeLocal area3 days per week
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