QC Administrator (d/f/m)
Novartis
Country: Slovenia
Location: Ljubljana (Sandoz)
Time Type: Full time
Posted On: November 19, 2024
Job Description Summary
The future is ours to shape.
Job Description
5500! is the number of batches of medicines we supply annually to the Slovenian, European, and global markets in the 14-member ESO (External Supplier Organisation) release team of Lek | Sandoz, which you will join as a QC Administrator.
As a QC Administrator, you will be responsible for the quality and timely inspection of the packaging and for the distribution of samples and documentation.
Your responsibilities include, but not limited to:
- Responsible for the archiving of Batch Records and release documents.
- Inspection of the packaging of medicinal products, checking that the packaging complies with the approved documentation.
- Compilation of documents for the release of medicines to the market.
- Reconciliation of priorities for the release of medicines to the market.
- Responsibility for personal and professional development.
- Other tasks as assigned by the supervisor, and tasks based on a specific appointment.
Essential Requirements:
- Secondary school degree (higher education degree is preferred) in pharmacy, chemistry or other related discipline.
- Basic knowledge of English and good knowledge of Slovene.
- Knowledge of Microsoft Office.
- Team spirit and good work ethic.
You’ll receive:
Employment at the most reputable employer in Slovenia offers Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), Unlimited learning and development opportunities.
Possible job locations: Slovenia (Ljubljana). For this position, we do not offer relocation.
We offer a temporary contract of one year (until 31.12.2025) with a probation period of 6 months.
You are kindly invited to submit your application, including your CV, by the 26th of November 2024.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
Commitment to Diversity & Inclusion:
Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpool
#Sandoz
Skills Desired
Continued Learning, Good Documentation Practice, Guideline, Qa (Quality Assurance), Quality Management, Regulation, Self-Awareness, Technological Expertise