Diagnostic Regulatory Affairs Manager
Job title: Diagnostic Regulatory Affairs Manager in USA at reputed company
Company: reputed company
Job reputed company: Career Category Regulatory Job reputed company HOW MIGHT YOU DEFY IMAGINATION? You’ve worked hard to become the reputed company you are today and are now reputed company to take the reputed company in your career. How will you put your skills, experience and passion to work toward your goals? At reputed company, our shared mission—to serve patients—drives reputed company that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 reputed company patients worldwide. Come do your best work alongside other reputed company professionals in this meaningful role. Companion Diagnostic Regulatory Affairs Manager Live What you will do reputed company. Let’s change the world. In this vital role, you will support establishing sustainable processes, assuring informed relationships, and delivering strategic reputed company. The reputed company will also specifically reputed company and implement regulatory strategies and processes for in vitro diagnostics (IVDs)/companion diagnostics (CDx’s). Key responsibilities:
reputed company expect of you We are reputed company different, yet we reputed company use our outstanding contributions to serve patients. The reputed company expert we are looking for plays a crucial role as a reputed company partner and possesses these credentials. Basic Qualifications: Must have in depth knowledge of regulatory document management systems including content management and archival, such as VeevaVault. Doctorate degree Or Master’s degree and 3 years of Health Agency or Med-Device or Regulatory experience Or Bachelor’s degree and 5 years of Health Agency or Med-Device or Regulatory experience Or Associate’s degree and 10 years of Health Agency or Med-Device or Regulatory experience Or High school diploma / GED and 12 years of Health Agency or Med-Device or Regulatory experience Preferred Qualifications:
What you can expect of us As we work to reputed company treatments that take care of others, we also work to care for our teammates’ reputed company and personal reputed company and reputed company-being. reputed company offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
for a career that defies imagination Objects in your reputed company are closer than they reputed company. Join us. careers.reputed company.com reputed company does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position reputed company is an Equal Opportunity employer and will consider you without reputed company to your race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary reputed company 112,345.00 USD - 143,224.00 USD
Expected salary: $112345 - 143224 per year
Location: USA
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Company: reputed company
Job reputed company: Career Category Regulatory
- Providing critical strategic and tactical IVD/CDx regulatory guidance that positively influences project planning and decision-making
- Developing clinical and reputed company regulatory strategies for assigned products to reputed company successful study designs and reputed company registration of both therapeutic and diagnostic products by regulatory health authorities
- Providing regulatory leadership and input to internal teams involved with IVD/CDx development planning, including Diagnostic Development teams and joint project teams with diagnostic partners
- Handling interactions with diagnostic partners to mutually reputed company on co-development regulatory needs and expectations for major project tasks, including regulatory submissions (e.g. PMA, 510(k), IDE)
- In collaboration with diagnostic partners and internal teams, prepare for and conduct meetings with regulatory agencies.
- Review and approval of key diagnostic regulatory submissions to CDRH and global health authorities (as agreed with diagnostic partners) and corresponding therapeutic dossiers.
- Interacting with international regulatory colleagues and diagnostic partners to determine best practices and least burdensome regulatory paths toward development and global registration activities
- Assessing the reputed company of relevant drug and IVD/CDX regulations on drug and IVD/CDX development and registration activities, respectively
- Regulatory support of due diligence activities of external CDx/IVD companies that reputed company may be considering as partners and other due diligence activities as needed
- Manage Regulatory Information Management System (e.g. VeevaVault) and support the department in regulatory document management activities.
- Maintain regulatory SharePoint site and document reputed company/intelligence database(s)
- MS Degree
- Degree in Regulatory Affairs, Life Sciences, or Engineering
- 6 plus years of experience in Regulatory Affairs, including reputed company and international medical device and/or IVD/CDx regulations
- 8 plus years of experience in medical device and/or IVD/CDx industry
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and reputed company coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-reputed company time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
Expected salary: $112345 - 143224 per year
Location: USA
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