About this role
Job Description Summary
The QC Expert supports the evaluation of analytical test results, method transfer, and method validation as well as equipment life-cycle activities.In addition, he is involved in continuous process improvement and digitalization within QC.
Job Description
Your Key Responsibilities:
Your responsibilities include, but not limited to:
- Planning and execution of method transfers and method validations
Evaluation of analytical test results from method transfers and method validations
Assessment of OOS results and deviations
Subject matter expert and point of contact for complex analytical and technical processes
Statistical evaluation of raw data, including trend analysis
Support of QC in continuous process improvement and digitalization
Review and approval of test protocols
Qualification activities for QC equipment
Life‑cycle management of QC equipment
What you’ll bring to the role:
Scientific degree, e.g., in chemistry, pharmacy, or a comparable field
Collaborating across boundaries.
Several years of professional experience in the pharmaceutical industry, ideally with expertise in instrumental analytics
Experience in QC within the pharmaceutical industry
Analytical and solution‑oriented mindset
Excellent organizational and planning skills
Very good English skills, both written and spoken
Strong GxP knowledge
You’ll receive:
Sandoz has an employee-first approach and that’s why your personal growth is so important to us. You will have access to Coursera and other learning platforms with more than 200,000 learning videos and 5000+ courses.
In addition to the various learning opportunities, we offer company benefits, such as:
30 days of annual leave
Holiday allowance
Additional rewards for special occasions (e.g. service length awards, marriage celebration, etc.)
Company pension schemes and capital formation benefits
Parental leave
Other offerings, such as bike leasing
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:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Hiring decisions are only based on the qualification for the position, regardless of gender, ethnicity, religion, sexual orientation, age and disability.
The law provides for severely disabled / equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you would like to request this, please let us know in advance as a note on your CV.
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Skills Desired
Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological IntelligenceOther facts
About Sandoz
Sandoz is the global leader in generic and biosimilar medicines.
Our Purpose is to pioneer access to medicines for patients globally. We are on a mission to drive innovation in the healthcare industry by freeing up resources sustainably and responsibly while continuing to address global health challenges such as antimicrobial resistance.
We are present in more than 100 countries and our medicines serve some 500 million people every year. We have two main global businesses: Generics - divided between standard generics and complex generics - and Biosimilars.
Read our community engagement guidelines: http://bit.ly/4ofoggc
What you'll do
- The QC Expert is responsible for planning and executing method transfers and validations, evaluating analytical test results, and assessing OOS results. They also support continuous process improvement and digitalization within QC and manage the life-cycle of QC equipment.
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