Post Market Surveillance Specialist – Fixed-Term

Emploi pas sur LinkedIn

🕒 il y a 1 mois

🇺🇸 États-Unis – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

👻 Score fantôme 30%

infoinfo

🗣️🇺🇸🇬🇧 Anglais requis

Postuler Maintenant
Trouver des Emplois à Distance Similaires

📊 Vérifiez votre score de CV pour ce poste

Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

Logo of Merit Medical Oncology

Merit Medical Oncology

5001 - 10000 employés

Fondée en 1987

🏥 Santé

💼 Conseil

📦 Logistique

💰 €4 248 192 Venture Round - Cianna Medical en 2016-10

Healthcare • Consulting • Logistics

Merit Medical Oncology est une division/spécialité de Merit Medical Systems consacrée aux dispositifs et solutions procédurales pour les interventions oncologiques. Elle fait partie de Merit Medical Systems, un fabricant mondial fondé en 1987 qui conçoit et commercialise des dispositifs médicaux jetables propriétaires utilisés dans les procédures interventionnelles, diagnostiques et thérapeutiques en cardiologie, radiologie, oncologie, soins intensifs et endoscopie. Merit Medical Oncology soutient les hôpitaux et les médecins du monde entier avec des produits (par exemple, biopsie, embolothérapie, drainage, et autres outils interventionnels liés à l'oncologie), la formation et l'éducation des cliniciens, la documentation réglementaire et des produits, ainsi que la distribution mondiale et le support client.

Description

• Maintain and implement improvement projects and provide training when needed • Interact with management, international regulatory affairs/quality assurance, and global regulatory bodies on adverse event reporting • Analyze complaints and recommend whether they are reportable to global regulatory bodies • Participate in complaint-related meetings to determine which complaints require adverse event reports • Review complaint investigations and recommend resolutions • Prepare and submit reports to global regulatory bodies within required timeframes • Maintain records for the Global Quality Assurance adverse event reporting system • Prepare for, participate in, and assist with FDA facility inspections, Notified Body Audits, Post Market Surveillance activities, and governmental inspections • Perform other duties and tasks as needed

🎯 Exigences

• Education and/or experience equivalent to a Bachelor’s Degree and three years of related experience in a Quality/Regulatory-related field • Knowledge of U.S. FDA regulations (21 CFR 803) • Knowledge of the Medical Devices Directive (93/42/EEC, as amended) • Knowledge of European Medical Device Regulation 2017/745 (MDR) • Knowledge of ISO 13485 Quality System Standards • Knowledge of Canadian Medical Device Regulations • Experience with global medical-device adverse-event reporting, including MDR, MPR, Vigilance, and TGA • Self-motivated and self-directing • Strong attention to detail and excellent time-management skills • Strong interpersonal skills and ability to communicate well verbally and in writing • Project-management experience • Demonstrated computer skills, preferably spreadsheets, word processing, databases, internet research, and other applicable software • Preferred: ASQ Certified Quality Auditor (CQA) • Preferred: Regulatory Affairs Certification (RAC Global) • Preferred: Experience with electronic submissions • Ability to meet physical demands including lifting up to 50 lbs., writing, sitting, standing, bending, visual acuity, color perception, depth perception, reading, and peripheral vision

🏖️ Avantages

• Medical/Dental & Other Insurances (eligible the first of month after 30 days) • Low Cost Onsite Medical Clinic • Two (2) Onsite Cafeterias • Employee Garden | Gardening Classes • 3 Weeks' Vacation • 1 Week Sick-Time • Paid Holidays • 401K • Health Savings Account • Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights

Postuler Maintenant

Emplois Similaires

🕒 il y a 1 mois

Solventum

10 000+ employés

🏥 Santé

📦 Logistique

💼 Conseil

Surgical Healing Specialist driving incision-management and wound-healing solution sales for Solventum, a healthcare technology company. Supporting operating-room teams, territory growth, customer education, and clinical adoption.

🇺🇸 États-Unis – Télétravail

💵 $158 000 - $217 250 / an

⏰ Temps Plein

🟠 Senior

🔴 Expert

🗣️🇺🇸🇬🇧 Anglais requis

🕒 il y a 1 mois

Texas Sports Academy

2 - 10

📚 Éducation

⚽ Sports

Elite figure skating mentor guiding Texas Sports Academy student-athletes through academics and high-level athletic development. Supporting focus, training habits, competition mindset, and parent communication remotely.

🇺🇸 États-Unis – Télétravail

💵 $25 / heure

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

🗣️🇺🇸🇬🇧 Anglais requis

🕒 il y a 1 mois

Hitachi

10 000+ employés

🚘 Automobile

🏗️ Construction

💼 Conseil

Tendering and Proposal Specialist developing bids, pricing strategies, and compliant submissions for Hitachi Energy’s Distribution Transformers business. Collaborating with sales, engineering, legal, and commercial teams.

🇺🇸 États-Unis – Télétravail

⏰ Temps Plein

🟢 Junior

🟡 Intermédiaire

🦅 Parrain de Visa H1B

infoinfo

🗣️🇺🇸🇬🇧 Anglais requis

🕒 il y a 1 mois

Upchurch

501 - 1000

🏗️ Construction

🏭 Fabrication

⚡ Énergie

Pipefitter installing and testing mechanical piping systems for Upchurch, a southeastern U.S. building engineering company. Reading plans, assembling diverse piping materials, supporting welders, and maintaining HVAC and process systems.

🇺🇸 États-Unis – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

🗣️🇺🇸🇬🇧 Anglais requis

🕒 il y a 1 mois

Otsuka Pharmaceutical Companies (U.S.)

1001 - 5000

💊 Pharmaceutique

🏥 Santé

🧬 Biotechnologie

Neuroscience Specialist advancing Otsuka’s innovative healthcare products through local HCP engagement. Driving territory planning, compliant sales presentations, speaker programs, and patient-outcome-focused customer support.

🇺🇸 États-Unis – Télétravail

💵 $107 362 - $166 750 / an

⏰ Temps Plein

🟢 Junior

🟡 Intermédiaire

🚫👨‍🎓 Aucun diplôme requis

🗣️🇺🇸🇬🇧 Anglais requis