Quality Assistant

Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:

• Career development with an international company where you can grow the career you dream of.
• Competitive salaries, bonus potential and excellent package of benefits.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

For our Core Diagnostics Division CDx we are currently looking for a well-motivated, hard-working talent to join our regional Quality Assurance team as a Quality Assistant.

The successful candidate will start on a 6-months fixed-term contract signed with external agency (with an opportunity to prolong after fruitful cooperation). This will be an office-based job requiring regular presence in our office in Warsaw.

Impact of the role:

• Supports Quality System compliance in a specific region or regions.
• Supports a specific process or processes for the whole Europe/EEMEAP as Subject Matter Expert (SME), its backup, or part of the team.
• Operates under Quality and Regulatory directives and Abbott policies and procedures.
• Follows local regulations and international industry/ Quality System standards.

What You'll do:

• Supports the Manager QA Region to ensure Europe/ EEMEAP and Region Quality System effectiveness and compliance.
• Performs internal and supplier audits.
• Supports external audits.
• Review & approve locally developed AdPromo material in local language on behalf of Regulatory Affairs.
• Supports the Europe/ EEMEAP common Quality System and QS processes: e.g. Field communications, supplier evaluation, audits and CAPA, AdPromo, document control and record keeping.
• Review Abbott policies & procedures, and update Quality documentation accordingly.
• Participates in Quality System improvements and implementation projects.

Required qualifications and background:

• Scientific background (i.e. Lab Technician, Biology, Chemistry, Pharma, M.D., Engineer) preferred.
• Prior relevant experience in QA, RA within diagnostics, medical devices or pharmacy is highly desirable (min. 1 year)
• Quality Assurance in a commercial affiliate at the diagnostic/ medical device/ pharmaceutical industry is preferred.
• Excellent command of written and spoken English is a must.
• Readiness to travel (approx. 10% of time).
• Experience to work in international environment/ projects is preferred.
• Ability to work in a hybrid model (4 days per week from the office).

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

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