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 complaint records, including intake, follow up, triage, system entry- and final response, involving Alcon devices, pharmaceutical products and OTC products. Complaints handling accountabilities reflect activities required to comply with local and international regulations, guidelines and applicable directives

KEY RESPONSIBILITIES:

Ensure compliance of the regional/country complaint handling process for all Alcon products, including intake, follow up and triage for reports of quality/technical complaints and Adverse Events in compliance with local and international regulations, guidelines and applicable directives.

Receive initial complaint from any source (ECPs, patients, internal Alcon personnel) and assure all information/data is accurately captured at point of contact

Maintain an understanding of information or date required to be collected of technical and AE complaints to assure compliance with regulations and directives

Manage technical and adverse event complaint records for assigned areas using designated safety systems

Review potential complaint data received via safety systems and other methods as required  

Perform intake/follow up/data entry activities and attached corresponding source documents in a timely manner per requirements and directives.

Perform all necessary reconciliation activities including for all customer-oriented programs in accordance with procedures

Triage/address calls from all sources for quality technical complaints, Adverse Events, and assist into the request for refund, request for replacement product and requests for credit

Adheres to require metrics for all complaint intake responsibilities

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

Closes files according to establish guidelines to meet required timelines

Maintain a working knowledge of company policies and procedures, departmental processes, and associated work instructions

Monitor the evolving local and international regulations, guidelines, and applicable directives, and inform regional/ global of the changes in a timely manner

Responsible country(ies): APAC and GEM (Including Thailand)

Key Performance Indicators (KPI)

Quality and timely reporting of KPI and customer response

Complaint and/or AE intake reporting compliance

No critical findings in audits or inspections

Customer feedback and satisfaction

Associate is authorized:

To manage any follow up with the complainant, and to update into the GPCMS

To prepare the final response according to the Quality Summary (prepared by Alcon's global device vigilance colleague) and forward the notification to the Healthcare Professional

To arrange the return of any product compliant sample to the manufacturer for investigation

To manage and work within Alcon representative into any customer and/or product responses, and feedback within agreeable timeline

To conduct reconciliation with Alcon representative and report out within agreeable timeline

WHAT YOU’LL BRING TO ALCON:

Tertiary qualification in optometry/ pharmacy/ ophthalmology/ medicine/ pharmacology/ biomedical science/ biomedical engineering/ chemistry/ biology/ nursing or other healthcare discipline

Languages:           

Fluent in English and Thai (spoken and written) – required

Fluent in Mandarin (spoken and written) – an advantage

Key Competencies/Behaviours:

Technically Competent.

Results Driven

Customer / Quality Focus

Empowerment / Accountability

Mutual Respect / Trust / Loyalty

Experience:           

1- 2 years of experience in pharmaceutical and medical device industries

Proven ability in implementing quality and documentation systems. 

Record of accomplishment of tracking complaints

Effective communicator

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

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