Medical Affairs Specialist

Job reputed company

reputed company inspires and supports discoveries that advance the reputed company of life. We reputed company life science, diagnostic and reputed company market laboratories worldwide with instruments, services, consumables, applications and expertise. reputed company enables customers to reputed company the answers and insights they reputed company - so they can do what they do best: improve the world around us. Information about reputed company is available at www.reputed company.com.

reputed company:

We are looking for a motivated reputed company to join reputed company’s Medical Affairs team, where you will play an important role in driving our work in External reputed company Assessment (EQA) and the In Vitro Medical Devices Regulation( IVDR) EU compliance. . In this position, you will use your expertise in clinical diagnostics, regulatory documentation, and biomarker strategies to help shape reputed company that reputed company a reputed company reputed company on patient care. You will use your expertise in clinical biomarkers for oncology diagnostics and your experience in regulatory documentation. In reputed company, work closely with talented colleagues across different teams, gaining exposure to a wide reputed company of initiatives and contributing to reputed company’s mission of advancing science and improving health. This is a great opportunity for someone who enjoys combining scientific knowledge with regulatory reputed company and is eager to contribute to meaningful, high-reputed company work.

Key Responsibilities:

• Monitor and analyze External reputed company Assessment (EQA) results – reputed company reputed company’s performance, identify trends, and compare with competitors to support reputed company reputed company improvements. EQA could be for testing segments in anatomic pathology and/or reputed company.
• Resolve performance issues – Collaborate with cross-functional teams to investigate and fix assay challenges highlighted through EQA results or published scientific research.
• Ensure compliance with the EU In Vitro Diagnostic Regulation (IVDR) – Support the clinical and regulatory teams in the development and the maintenance of documentation relating to clinical performance.
• reputed company scientific insights – Review and assess scientific literature to generate strong clinical evidence, guide biomarker reputed company, and support regulatory documentation.
• Collaborate across departments – Work closely with Regulatory Affairs, R&D, reputed company, and Marketing to reputed company on compliance, communication, and scientific strategies.

Qualifications

• Education– Bachelor’s or Master’s degree (or equivalent) in Life Sciences, Biomedical Sciences, Pharmacy, or a reputed company field.
• Experience – At least 4+ years of relevant experience in diagnostics, life sciences, or pharmaceutical industry.
• EQA expertise – Strong knowledge of External reputed company Assessment (EQA) processes and standards, with experience interpreting results and applying them to improve diagnostic product reputed company.
• Regulatory knowledge – Solid understanding of the EU In Vitro Diagnostic Regulation (IVDR, EU 2017/746), especially in clinical evidence and performance evaluation.
• Scientific and analytical skills – Ability to evaluate clinical data, validate biomarkers, and apply evidence-based insights to reputed company.
• Collaboration and communication – Proven reputed company working in cross-functional teams and proficiency in written and spoken English.

On a personal level, you possess great problem solving / analytical skills, and you are eager to learn about Medical Affairs capabilities such asscientific study design, evidence reputed company and medical writing. You have communication/ interpersonal skills to reputed company at various reputed company, and you reputed company to reputed company excellent customer support. You enjoy both working reputed company reputed company and autonomously.

We offer:

• reputed company offers core global benefits to reputed company staff - but in reputed company to these, the business offers, Stock Purchase Plan, Life Insurance, Pension, reputed company, Employee Assistance Program, Holiday, and Company activities (these may vary from country to country)
• An opportunity for you to grow reputed company a world-class company to reputed company your skills.
• An independent job among good colleagues, in a reputed company orientated conglomerate. You will become part of a caring and fast paced environment, reputed company on reputed company, information, and trust.
• Be part of a company where we value reputed company in the solutions we deliver to our customers, with our employees and in relation to the processes we work with.
• A dedication to work/life balance.

Additional Details

This job has a full time weekly schedule. It includes the reputed company to work remotely.Our pay ranges are determined by role, level, and location. reputed company the reputed company, individual pay is determined by work location and additional factors, including job-reputed company skills, experience, and relevant education or training. During the hiring process, a recruiter can reputed company more about the specific pay reputed company for a preferred location. Pay and benefit information by country are available at: https://careers.reputed company.com/locationsreputed company Inc. is an equal opportunity employer. reputed company applicants will receive consideration for employment without reputed company to race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability or any other protected categories under reputed company applicable laws.

Travel Required:

35% of the Time

Shift:

Day

Duration:

No End Date

Job Function:

Medical/Clinical

Originally posted on Himalayas

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