Seniority level:
General manager
Skills:
Leadership
, 3 yrs.
Team Management
, 3 yrs.
Team Leadership
, 3 yrs.
Team Oriented
, 2 yrs.
Languages:
English
C1 - Advanced
Experience:
8 yrs.
minimum
in
Life sciences
Monthly salary (gross):
3000
€
Contract type:
Full-time
Location:
Vilnius
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Job description
Quality Director
Position: Quality Director / Head of Quality Unit
We are looking for:
- A leader who can take over an existing quality system of a pharmaceutical company, supervise it, improve it, implement innovations, and ensure compliance with Good Manufacturing Practice requirements and European Union and Lithuanian legislation.
- A team member who would like to contribute to the creation and maintenance of a quality system capable of providing global services to international pharmaceutical companies.
Requirements:
- Strategic thinking and leadership skills.
- Ability to take responsibility.
- Ability to lead the Quality Assurance and Control team.
- Proficiency in English, ability to communicate with foreign clients.
- Proficiency in Lithuanian, ability to communicate with local authorities.
- Managerial experience (minimum 1 year).
- Excellent knowledge of Good Manufacturing Practice requirements.
- Minimum of 3 years of experience in working with GMP and Quality Assurance or Quality Control in a pharmaceutical company.
- Ability to fill out applications to the State Medicines Control Agency (VVKT) would be an advantage.
- Ability to find solutions and creativity.
- Positivity, problem-solving, and openness.
- Ambition and willingness to learn how to create and maintain a quality system that meets global standards.
Main Responsibilities:
- To form and maintain the Quality Assurance and Quality Control team.
- To take over an existing Quality system, supervise it, improve it, and digitize it.
- To implement innovations and ensure compliance with Good Manufacturing Practice requirements and European Union and Lithuanian legislation.
- To lead the Quality Assurance and Quality Control teams.
- To supervise and organize internal and external audits.
- To communicate with the State Medicines Control Agency and timely submit applications for compliance with GMP and Manufacturing licenses.
- To prepare and supervise Quality agreements.
- To mediate with other company groups and individuals to ensure timely project completion.
- To develop, nurture, and care for the Quality System within the company, provide recommendations for improving the Quality System, and ensure the qualification of oneself and the team.
About Profarma
European Laboratory holding MIA license as well as GMP certificate and serving Pharma Industry with EU Batch Release Testing, QP Batch Release, and Product Development. Profarma‘s expertise includes small molecules, peptides, and biologics, including active pharmaceutical ingredients (API), intermediate stages, and final drug products. Our clients come to us at different stages of the drug product life cycle, starting from early development and drug registration to routine commercial supply for the EU market. We help to assure product quality by performing QC testing and opening doors to complex European markets.
The application period for this job listing has expired.