You will conduct pharmaceutical process development studies and document the results while supporting analytical testing and the manufacturing of drug product samples, all while ensuring safety and compliance.
Anforderungen
- •Master's degree or equivalent experience
- •Knowledge of fill and finish process for pharmaceuticals
- •Experience in a pharmaceutical process development lab preferred
- •Excellent collaboration skills
- •Flexible and proactive mindset
- •Eagerness to learn
- •English required, good working level
Deine Aufgaben
- •Conduct small-scale pharmaceutical process development studies.
- •Document data in accordance with lab procedures.
- •Evaluate results and summarize findings in short reports.
- •Implement and execute analytical tests for pharmaceutical development.
- •Support manufacturing of non-GMP drug product samples.
- •Apply aseptic techniques while ensuring compliance with health and safety standards.
Original Beschreibung
# Intern Process Development (Filling and Lyophilisation) 80-100% (m/f/d)
**CH - Basel** | **Full time**
Due to an increase of workload in our department, we are looking for an intern to support plan and perform pharmaceutical development studies for liquid and lyophilized parenteral drug products of biologics (e.g. monoclonal antibodies, novel formats, ADCs, peptides) under the responsibility of a Scientist.
Key responsibilities:
Complete in the laboratory and report small scale pharmaceutical process development studies for parenteral (mixing hold time, VHP stress, filtration, filling behaviour and lyophilization) studies under the supervision of a senior scientist.
* Document data following applicable lab procedures, current documentation practices and aligning with data integrity standards, evaluate results and summarize in short reports
* Support implementation and execution of analytical tests for pharmaceutical development (e.g. HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, visible particles, subvisible particles).
* Support manufacturing non-GMP drug product samples for supportive stability studies and preclinical use (e.g. GLP tox studies) applying aseptic working techniques. Ensure compliance to health and safety standards.
Key requirements:
* Masters degree or equivalent experience
* Knowledge in the process steps of fill and finish for parenteral pharmaceutical products. Ideally experience in a process development lab for pharmaceuticals.
* A strong standout colleague with excellent collaboration skills
* Flexible, proactive, and eager to learn
* Languages: English required (proficiency, or at a minimum good working level in written and spoken language)
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.