Scientist - Design Control Documentation job opportunity at Agilent Technologies.

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Agilent Technologies Scientist - Design Control Documentation
Experience: General
Pattern: full-time
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loacation Denmark-Glostrup, Denmark
loacation Denmark-Glostr..........Denmark

Job Description Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and   expertise . Agilent enables customers to gain the answers and insights they   seek , so they can do what they do best: improve the world around us. Information about Agilent is available at   www.agilent.com .   Job Description:  We are seeking a highly motivated and detail-oriented   scientist for   Design Control Documentation. The successful candidate will focus on the design control documentation of medical devices   for   diagnostic   u se   within the fields of   tissue-based   pathology   assays   such as   immunohistochemistry .     Key Responsibilities:   Develop, review, and maintain design control documentation in compliance with regulatory requirements , such as   writing   Design Input and Output documentation,   Production Transfer documentation ,   protocols and reports including data analysis for   stability,   verification and   validation studies   of antibody assays for diagnostic use .   Collaborate with cross-functional teams to ensure documentation accuracy and completeness.   Support the design and development process by providing expertise in documentation standards and practices.   Ensure timely updates and revisions of documentation as needed.   About Our Team:  The Reagent Design team is part of the New Product Introduction R&D department. We are a team of 1 2   employees skilled in design control documentation of   assays   for diagnosti c use   within the fields of   tissue-based pathology assays such as   immunohistochemistry   and ISH/FISH   molecular assays . Our team is dedicated to excellence and innovation in medical diagnostics.   Work Environment:   We cultivate a collaborative and supportive   work environment where teamwork and cross-functional collaboration are highly valued.   This approach not only enhances creativity but also ensures that everyone feels valued and supported in their roles.   Qualifications Master's degree or higher in a relevant field (e.g.,   Biochemistry,   Biomedical Engineering, or related discipline).   Experience with design control documentation in the medical device industry.   Knowledge of regulatory requirements and standards (e.g., ISO 13485, FDA 21 CFR Part 820).   Familiarity with immunohistochemistry and   ISH/FISH molecular assays   is highly desirable.   Strong attention to detail and excellent organizational skills.   Ability to work independently and as part of a team.   Excellent written and verbal communication skills in English.     What We Offer:   A chance to be part of   New Product Introduction R&D   developing   products to the benefit of cancer patients, worldwide   A position in an international and dynamic working place with exciting challenges and opportunities   Great colleagues and   a strong team   spirit   Many opportunities for personal career and   expertise   development   Outstanding company culture   Company pension scheme, individual bonus plan, private health care, medical & life insurance   Additional Details This job has a full time weekly schedule. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws. Travel Required: Occasional Shift: Day Duration: No End Date Job Function: R&D

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