Johnson & Johnson Careers

Quality Assurance Specialist

Vilnius, Lithuania
Quality (Generalist)


Job Description

Requisition ID: 1805696303W

At Janssen, we are dedicated to addressing and solving some of the most important unmet medical needs of our time in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases.  Driven by our commitment to patients, we bring innovative products, services and solutions to people throughout the world. Janssen is a pharmaceutical company of Johnson & Johnson.  Please visit www.janssen.com for more information 
 
Janssen, part of Johnson & Johnson Family of Companies is now looking for Quality Assurance Specialist:
 
Quality Assurance Specialist
Located in Lithuania
Full-time contract
 
Role Overview:
The Quality Assurance Specialist is responsible for the quality of, and meeting the applicable requirements for, the products that the LOC markets, or the products that it produces for other companies. He/she is also responsible for compliance with the elements of the Johnson & Johnson Quality Policy and J&J QMS that are applicable to the GMP/GDP activities the LOC / Cluster undertakes.
 
As Quality Assurance Specialist, you will have the following areas of responsibility:
  • As part of the Baltic Quality team maintain, develop and improve the Quality Management System.
  • Responsible for GDP compliance of UAB Johnson & Johnson and branches.
  • Handle quality related issues; deviations, product complaints, change controls etc.
  • Close collaboration with internal teams as supply chain, pharmacovigilance and regulatory affairs.
  • Be the quality contact person for customers and suppliers of Janssen Baltic.

Qualifications
Qualifications and experience of the successful candidate:
  • Pharmaceutical degree
  • 2-3 years of experience in either pharmaceutical industry or wholesaling.
  • Good knowledge of national and European GDP is an advantage
  • Experience from managing of all common quality systems/ processes, such as: Deviations, CAPAs, Complaints, etc. is an advantage
  • Understanding of pharmaceutical product development, qualification, manufacturing, packaging, validation, testing, release and distribution processes
  • Your self-leadership skills are well developed, and you work independently
  • Proven self-starter with good initiative and enthusiasm
  • Strong work ethic, structure and results orientation
  • Flexible and comfortable with ambiguity in a dynamic and changing environment
  • Able to prioritize in a highly matrixed environment
  • You are a fluent speaker of Lithuanian and have proficiency in oral and written English.
  • You are proficient in common computer programs (Microsoft Office and others).
     
     
If you are interested in this role and you fulfill the requirements set above, do not hesitate to send us your CV and cover letter in English.

Primary Location
Lithuania-Vilnius--
Organization
UAB Johnson & Johnson (7766)
Job Function
Quality (Generalist)
Requisition ID
1805696303W