Supervisor Complaint Processing
Supervisor Complaint Processing
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Provide support to the global team for processing complaints and inquiries from internal and external customers about medical devices and complaints such as sales agents sales representatives manufacturing commercial hospital or medical sites in addition to leading the team of analysts ensuring compliance with regulatory requirements in the process as well as adequate team performance. In addition it must guarantee compliance with corporate procedures as well as product quality customer satisfaction in addition to maintaining the quality system while ensuring the profitability of the same process.
MAJOR RESPONSIBILITIES
- Provide daily direction to the local team of analysts responsible for processing complaints.
- Have a futurefocused perspective to ensure that trends are ahead of trends.
- Managing the application of policies procedures and new product launches that impact the complaint processing department.
- Provide support as a complaint processing expert in internal and external audits.
- Ensure that complaint records meet the appropriate requirements and ensure that the equipment is kept up to date with current obligations.
- Lead internal controls to ensure required performance compliance for the team in charge.
- Provide support when required in other functional areas of the PMQA department such as Intake or reporting.
- Performer of quality activities such as CAPAs internal audits change control or procedures.
- Ensure the development of its staff in charge through the tools provided by the organization.
- Prepare and submit data related to product complaints.
- Ensure continuous improvement related to error control in data integrity through good documentation practices.
Qualifications :
- University degree in technological careers engineering or with a scientific approach such as: chemistry pharmacy biology microbiology.
- Advanced knowledge of the English language at least B2 C1 (preferred) of the European framework.
- Work experience of at least 3 years in the regulated medical device industry (GMPs) and quality occupying a position at a technical or professional level.
- Work experience of at least 1 year supervising staff Experience in project execution
- Technical knowledge in regulations/standards: FDA 21 CFR part 803 820 EU MDR ISO 13485:2016 (Preferred)
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
