QA Complaint Handling Associate (Cantonese/ Mandarin Speaker)

Alcon · Other US Location

Company

Alcon

Location

Other US Location

Type

Full Time

Job Description

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

POSITION OVERVIEW:

Responsible for day-to-day case management of quality technical and adverse event (AE) complaint records, including intake, acknowledgement, follow up, triage, system entry and final response, involving Alcon devices, pharmaceutical products, over-the-counter products. Complaint handling accountabilities reflect activities required to comply with local and international regulations, guidelines and applicable directives.

Responsible for day-to-day unsolicited on-label medical inquiries from eye care professionals (ECP), consumers, and internal partners, including providing responses involving Alcon devices, pharmaceutical products, and over-the-counter products. Triage requests appropriately and direct to the appropriate department if they involve off-label information.

KEY RESPONSIBILITIES:

  • Receive initial complaint from any source (e.g. ECP, patients, internal/ external Alcon representatives) and assure all information/ data is accurately captured at point of contact

  • Maintain an understanding of information/ data required to be collected for technical and AE complaints to assure compliance with regulations and directives

  • Manage technical and AE complaint records for assigned area(s) using designgated safety system(s)

  • Review potential complaint data received via safety system(s) and other methods, as required.

  • Is cognizant of, and works efficiently within applicable time zones

  • Performs all necessary reconciliation activities including for all customer oriented programs in accordance with procedures

  • Triage/ address calls from all sources for quality technical complaint, AE, requests for refund/ replacement product and credit

  • Adheres to required metrics for all complaint handling responsibilities

  • Arrange for replacement, product return and shipping of samples to QA sites for analysis

  • Closes files according to established guidelines to meet required timelines

  • Maintain a working knowledge of:

- Company policies and procedures, departmental processes, and associated work instructions
- Evolving local and international regulations, guidelines and applicable directives

- Alcon products for assigned therapeutics area(s) and corresponding documentation (Product Inserts, Direction for Use (DFU), Manuals, Promotional Materials)
- Eye anatomy, common diseases, ophthalmic procedures, terminology
- Complaint management system, safety database and reporting tools
- Informs management of potential safety issues, emerging trends and/or concerns

  • Ensure that a business continuity plan is in place which is aimed at guarantee the uninterrupted availability of key vigilance processes and activities, or mitigate the impact of an unwanted event by means of measures and procedures enabling efficient and effective business resumption and/ or recovery, exists and has been test-ed accordingly

  • Ensure Alcon associates, 3rd party business partner, external vendors are adequately trained in product complaint and/or adverse event reporting

  • Ensure the country is inspection ready for both internal audits and inspection from health authorities

  • Maintain and analyse the complaint statistic reports in regularly

  • Perform and manage on the QA activities, including but not limited to DOH audit, CAPA system and ad-hoc tasks in QA team

  • Monitor vendor’s working process to ensure safety reporting meet the country regulations

  • Ensure potential gaps and problems are solved timely and mitigate impact, if applicable

  • Management and maintenance of all relevant country vigilance

WHAT YOU'LL BRING TO ALCON:

  • Minimum: graduation in science.

  • Ophthalmology/ Eye care experience desirable

  • Desirable: university degree in optometry/ pharmacy/ ophthalmology/ medicine/ pharmacology/ biomedical science/ biomedical engineering/ chemistry/ biology/ nursing or other healthcare discipline.

  • Must be fluent in both written and spoken English, Traditional Chinese, and Cantonese. Preferably with working experience in a QA background

  • 1 year of experience in customer service, complaints handling, quality management system or similar

  • Experience working within multinational pharma companies or medical device company desirable

  • Comprehensive understanding of national and international regulations for medical device vigilance and pharmacovigilance, medical terminology

HOW YOU CAN THRIVE AT ALCON:

  • Opportunity to work with a leading global medical device company

  • Collaborate with a diverse and talented team in a supportive work environment

  • Competitive compensation package and comprehensive benefits

  • Continuous learning and development opportunities

Alcon Careers
See your impact at alcon.com/careers

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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Date Posted

09/10/2024

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