3 Medical Professionals jobs in Aberdeen
Senior Medical Aesthetician
AB10 1AA Aberdeen, Scotland
£38000 Annually
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Posted 2 days ago
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Job Description
Our client is seeking a highly experienced and qualified Senior Medical Aesthetician to join their innovative clinic in Aberdeen, Scotland, UK . This role offers a unique opportunity to work with advanced aesthetic technologies and provide a wide range of non-surgical cosmetic treatments. The position includes a hybrid work arrangement, blending client-focused clinic duties with remote administrative and consultation possibilities.
The successful candidate will be responsible for performing advanced skincare treatments, laser therapies, chemical peels, micro-needling, and other medical-grade aesthetic procedures. Conducting thorough client consultations, assessing skin conditions, and developing personalized treatment plans to achieve desired outcomes will be paramount. You will also be involved in recommending and retailing premium skincare products, educating clients on product usage, and maintaining detailed client records.
As a Senior Aesthetician, you will be expected to stay updated on the latest trends and techniques in medical aesthetics. You may also be involved in training and mentoring junior staff, contributing to treatment protocol development, and ensuring the clinic adheres to the highest standards of safety and hygiene. Excellent interpersonal skills are required to build strong client relationships and provide an exceptional, personalized service. A deep understanding of dermatological principles and advanced treatment modalities is essential.
Qualifications and Skills:
The successful candidate will be responsible for performing advanced skincare treatments, laser therapies, chemical peels, micro-needling, and other medical-grade aesthetic procedures. Conducting thorough client consultations, assessing skin conditions, and developing personalized treatment plans to achieve desired outcomes will be paramount. You will also be involved in recommending and retailing premium skincare products, educating clients on product usage, and maintaining detailed client records.
As a Senior Aesthetician, you will be expected to stay updated on the latest trends and techniques in medical aesthetics. You may also be involved in training and mentoring junior staff, contributing to treatment protocol development, and ensuring the clinic adheres to the highest standards of safety and hygiene. Excellent interpersonal skills are required to build strong client relationships and provide an exceptional, personalized service. A deep understanding of dermatological principles and advanced treatment modalities is essential.
Qualifications and Skills:
- NVQ Level 3 or 4 in Beauty Therapy, with advanced certifications in medical aesthetics, laser treatments, or similar.
- Minimum of 5-7 years of hands-on experience in a clinical aesthetic setting.
- Proficiency in performing a wide range of aesthetic treatments (e.g., laser hair removal, skin rejuvenation, injectables administration support).
- In-depth knowledge of skin anatomy, physiology, and common skin concerns.
- Experience in client consultation, treatment planning, and product recommendation.
- Strong understanding of health and safety regulations within the aesthetic industry.
- Excellent communication, empathy, and client relationship-building skills.
- Ability to work independently and as part of a dedicated team.
- Commitment to continuous professional development.
- Experience with electronic health records (EHR) or clinic management software.
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Senior Medical Affairs Manager - Oncology
AB25 1BB Aberdeen, Scotland
£70000 annum + ben
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Posted 2 days ago
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Our client, a rapidly growing and innovative pharmaceutical company with a strong focus on oncology, is seeking a highly experienced Senior Medical Affairs Manager. This role is pivotal in developing and executing the medical strategy for key oncology products, ensuring alignment with regulatory requirements and commercial objectives. The position offers a hybrid working arrangement, combining essential office-based collaboration with the flexibility of remote work for specific tasks and planning. You will be responsible for engaging with key opinion leaders (KOLs), scientific societies, and patient advocacy groups to gather insights, present scientific data, and support the clinical development and commercialisation of our client's portfolio. The ideal candidate will possess a profound understanding of oncology, clinical trial design, and the pharmaceutical regulatory landscape. Key responsibilities include developing medical education materials, organising scientific advisory boards, managing medical information requests, and contributing to the development of clinical trial protocols and publications. You will also play a crucial role in the medical review of promotional materials, ensuring scientific accuracy and compliance. The successful applicant will have outstanding communication, presentation, and interpersonal skills, with the ability to build strong relationships with both internal and external stakeholders. Experience in medical affairs within the oncology therapeutic area is essential. This role is based in the vibrant city of **Aberdeen, Scotland, UK**, offering a blend of strategic engagement and scientific leadership. Join a dedicated team committed to advancing cancer treatment and improving patient outcomes through scientific excellence and strategic medical affairs planning. Our client fosters a culture of collaboration, innovation, and continuous learning, making this an exciting opportunity for career growth in medical affairs.
Responsibilities:
Responsibilities:
- Develop and execute the strategic medical affairs plan for assigned oncology products.
- Engage with Key Opinion Leaders (KOLs) and scientific experts to foster relationships and gather insights.
- Support the planning and execution of medical education initiatives and scientific exchange programs.
- Provide scientific and clinical input into the development of marketing and promotional materials, ensuring compliance.
- Organise and manage scientific advisory boards and expert panel meetings.
- Respond to complex medical information queries from healthcare professionals.
- Contribute to the development and review of clinical trial protocols and study designs.
- Review and approve abstracts, posters, and publications arising from clinical research.
- Collaborate with R&D, clinical development, and commercial teams to ensure strategic alignment.
- Stay current with scientific literature, clinical trial data, and regulatory guidelines in oncology.
- Advanced degree (MD, PharmD, PhD) in a life science or medical field.
- Minimum of 5 years of experience in Medical Affairs, Medical Science Liaison (MSL), or related roles within the pharmaceutical industry.
- In-depth knowledge of the oncology therapeutic area and relevant disease states.
- Strong understanding of clinical trial processes, regulatory affairs, and pharmacovigilance.
- Demonstrated ability to build and maintain strong relationships with KOLs and healthcare professionals.
- Excellent written and verbal communication, presentation, and interpersonal skills.
- Experience in developing and reviewing medical education materials and promotional content.
- Ability to work effectively in a hybrid environment and manage time efficiently.
- Strategic thinking and a results-oriented approach.
- Familiarity with data analysis and interpretation relevant to clinical research.
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1
Remote Senior Quality Assurance Engineer - Medical Devices
AB10 1AD Aberdeen, Scotland
£70000 Annually
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Posted 2 days ago
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Job Description
Our client, a pioneering medical device manufacturer dedicated to improving patient outcomes through advanced technology, is seeking a highly skilled Senior Quality Assurance Engineer for a fully remote position, ideally located within or near Aberdeen, Scotland, UK . This pivotal role will involve ensuring the highest standards of quality and compliance in the design, development, and manufacturing of our innovative medical products. You will be responsible for developing and implementing comprehensive quality management systems in accordance with ISO 13485 and other relevant regulatory standards; conducting internal and external audits; managing the CAPA (Corrective and Preventive Actions) process; overseeing risk management activities; collaborating with R&D and manufacturing teams to ensure design controls are met; preparing and reviewing validation and verification documentation; leading quality-related investigations and driving continuous improvement initiatives; and maintaining all quality documentation and records. The ideal candidate will possess a Bachelor's degree in a relevant engineering or scientific field, with a minimum of 7 years of experience in quality assurance within the medical device industry. A deep understanding of regulatory requirements (FDA, CE Marking) and quality standards (ISO 13485, ISO 9001) is crucial. Strong analytical skills, meticulous attention to detail, and excellent problem-solving capabilities are essential. Proven experience in auditing, CAPA management, and risk assessment is required. Excellent communication and interpersonal skills are necessary for effective collaboration with cross-functional teams and regulatory bodies. As a remote employee, you must be a self-starter with strong organizational skills and the ability to work independently and proactively. This is an excellent opportunity to join a forward-thinking company and make a significant impact on the quality and safety of life-changing medical technologies. If you are a seasoned QA professional with a passion for excellence in healthcare, we invite you to apply.
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