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求人Boston Scientific

Quality Specialist I (Complaints Investigations)

Boston Scientific

Quality Specialist I (Complaints Investigations)

Boston Scientific

Cork, Ireland | N/A

·

On-site

·

Full-time

·

2mo ago

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

 

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

 

Advancing possibilities for a brighter tomorrow

 

We are seeking a Quality Specialist I on a permanent basis to join our team. 

 

Job Purpose: 

The Complaints Investigator will be responsible for investigating customer complaints related to pharmaceutical products, ensuring thorough documentation of findings within MasterControl. The role requires high attention to detail, excellent documentation skills, and the ability to work independently and collaboratively across teams. The successful candidate will support the maintenance of quality standards and regulatory compliance, contributing to continuous improvement in complaint handling processes.

 

 

Key Responsibilities 

  • Investigate and document customer complaints for pharmaceutical products to a high standard within MasterControl.
  • Conduct root cause analysis and risk assessments as part of complaint investigations.
  • Collaborate with cross-functional teams (Quality Assurance, Pharmacovigilance, Regulatory, Operations and Technical Team) to resolve product issues and support process improvements.
  • Ensure compliance with relevant cGxP regulatory requirements and internal procedures.
  • Prepare clear, accurate, and timely investigation reports and maintain complete records of all complaint activities.
  • Present findings and compliant processes during internal and external audits.
  • Participate in training programs, including an initial 10–12 week period in Farnham, UK.
  • Support continuous improvement initiatives in complaint handling and documentation.
  • Maintain up-to-date knowledge of pharmaceutical quality systems, regulatory requirements, and industry trends.
  • Support the Pharmaceutical Quality System team initiatives and activities
  • Initiates and writes/updates required procedures to support activities.
  • Identifies deviations from standard practices, evaluates their impact, and determines corrective actions.

 

Requirements

  • Level 8 Honours Bachelor Degree in Quality or related discipline.
  • 3 + years’ experience working in Pharmaceutical industry (Ideally in a QA role)
  • Excellent understanding and hands-on working knowledge of cGMP, quality and regulatory requirements.
  • Previous experience in a Quality, or Manufacturing background, particularly in relation to pharmaceutical quality systems
  • Strong communication skills, both verbal and written, with good interpersonal skills.
  • Skilled in using Microsoft Office applications.
  • Demonstrated ability to work with cross functional organizations in a dynamic manufacturing environment to solve problems.
  • Working knowledge and understanding of FDA, HPRA, and the pharmaceutical industry quality requirements and associated with manufacturing controls desirable
  • Experience in problem solving and process improvement methodologies desirable
  • Post Market, Complaint investigation and CAPA experience desirable

 

 

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

To search and apply for open positions, visit: https://bostonscientific.eightfold.ai/careers

 

At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer.  Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email TalentAcquisitionIre@bsci.com

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Boston Scientificについて

Boston Scientific

Boston Scientific Corporation (BSC) is an American biotechnology and biomedical engineering firm and multinational manufacturer of medical devices used in interventional medical specialties, including interventional radiology, interventional cardiology, peripheral interventions, neuromodulation,...

10,001+

従業員数

Marlborough

本社所在地

$58B

企業価値

レビュー

3.0

10件のレビュー

ワークライフバランス

2.5

報酬

2.8

企業文化

2.7

キャリア

3.2

経営陣

2.3

45%

友人に勧める

良い点

Friendly and helpful coworkers

Good benefits and health insurance

Meaningful work creating life-saving devices

改善点

Poor management and leadership

Poor work life balance and overtime

Unprofessional workplace culture

給与レンジ

18件のデータ

Junior/L3

Senior/L5

Junior/L3 · Biomedical Engineering (Entry-level)

1件のレポート

$78,100

年収総額

基本給

$71,000

ストック

-

ボーナス

$7,100

面接体験

5件の面接

難易度

3.0

/ 5

期間

14-28週間

面接プロセス

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Technical/Behavioral Interview

5

Final Round Interview

6

Offer

よくある質問

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Problem Solving