Assoc Regulatory Affairs Spec
Job Summary
At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.
Come strengthen your specialized skills and grow your experience. We will support you with the training mentorship guidance and networks you need to advance empowering you to work in the way that suits you best. Together we can take on challenges that will transform the future of healthcare. Join us to build a career that changes lives. This position will be based in Colombia Bogotá in a hybrid work model.
Responsibilities may include the following and other duties may be assigned.
- Direct or perform coordination and preparation of document packages for regulatory submissions from all areas of company internal audits and inspections
- Lead or compile all materials required in submissions license renewal and annual registrations
- Recommend changes for labeling manufacturing marketing and clinical protocol for regulatory compliance
- Monitor and improves tracking / control systems
- Keep abreast of regulatory procedures and changes
- May direct interaction with regulatory agencies on defined matters
- Recommend strategies for earliest possible approvals of clinical trials applications
Required Knowledge and Experience:
- Bachelors degree in Pharmaceutical Chemistry Biomedical Engineering Medicine Chemical Engineering or related field and/or practical experience in regulatory processes.
- 0-1 year of relevant experience in regulatory affairs within medical device companies
- Fluency in English (minimun B2 level required)
- Experience preparing/validating renewing and modifying health registrations.
- Experience working with regulatory agencies
Nice to Have:
- Experience with medical device regulatory registrations
- Experience in internal and external audits and CAPA (Corrective and Preventive Actions)
- Certifications in Good Practices (GMP GDP) and ISO 13485
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position but they are not an exhaustive list of all the required responsibilities and skills of this position.
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits resources and competitive compensation plans designed to support you at every career and life stage.
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission to alleviate pain restore health and extend life unites a global team of 95000 passionate people.
We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab to the factory floor to the conference room every one of us experiments creates builds improves and solves. We have the talent diverse perspectives and guts to engineer the extraordinary.
Learn more about our business mission and our commitment to diversity here
About Company
About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an excit ... View more