Thermo Fisher Scientific Jobs

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

When you’re part of Thermo Fisher Scientific, you’ll do ambitious work, and be a member of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.

Do you want to be part of our journey into the future? We produce products which are used in break-through technologies, lifesaving assays and clinical applications that demand a high attention to quality assurance in all steps of the production and control processes. Our customers are world leading pharma and diagnostics companies which have chosen us as their business partner. This means that we as a company must continue to develop and improve our quality assurance systems on an elite level.

Quality Specialist

Vilnius

We are now looking to find a new colleague to join our Quality Shared Service Team based in Vilnius. The team is a highly motivated with a passion for providing the quality services our customers rely upon.

Your key responsibilities will be to:

• Manage Vilnius Site CoC (Certificate of Conformance) requests by ensuring smooth and timely document preparation and maintaining effective communication with responsible departments;

• Handle global CoA (Certificate of Analysis) and CoO (Certificate of Origin) requests: directly communicate with customers and specific departments of the Company in order to ensure fast and high-quality dissemination of information;

• Support the customer complaint management process for equipment manufactured at the Singapore Site: collect data from different sources/databases, visualize data according to a template, perform a summarized complaint data analysis within the stipulated time frame;

• Serve as a backup for global and Site-specific documents‘ management, including reviewing, correcting and releasing documents in OCPLM (electronic document management system);

• Maintain and update standard work procedures and instructions related to processes;

• Participate in and lead projects related to these activities;

• Participate in the development and implementation of management systems in the Company, initiate their improvement;

• Actively use PPI tools and methods: participate and lead JDI and Kaizen, go to GEMBA walks and implement 5S.

Who we are looking for:

• You have a strong desire for continuous improvement;

• Your work is of high quality, and you transfer your standards and expectation of quality to your colleagues;

• You are service minded and helpful to others;

• You empower and communicate well with everyone and at all levels in-house;

• You thrive on influencing others and are results driven;

• You enjoy working independently as well as in team settings;

• You are highly organized, a strong self-starter, detailed and patient.

Experience/Qualifications needed to succeed:

• Bachelor's degree or higher (natural sciences is an advantage);

• Proficiency in English language (spoken and written);

• Proficiency in computer applications and MS Outlook, Word, Excel;

• Knowledge of Good Documentation Practice requirements is an advantage;

• Knowledge of ISO 13485 and/or ISO 9001 Quality Management Systems is an advantage;

• Experience in Medical Device or Pharmaceutical Industry is an advantage.

We Offer:

• The innovative environment of the rapidly growing international company.

• Hard-working, supportive working team and management with outstanding development possibilities to increase your potential.

• Monthly salary from 1980 to 2970 Eur before taxes and additional benefits package.

Compensation and Benefits

The salary range estimated for this position based in Lithuania is €23 800,00–€35 650,00.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.