4 дня назад
Scientist Process Development
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientist Process Development (Pharmaceutical Process Development): Executing laboratory studies for liquid and lyophilized parenteral drug products, including biologics, with an accent on fill-finish processes, aseptic techniques, and pharmaceutical analytics. Focus on designing and documenting development studies, qualifying laboratory equipment, evaluating scientific data, and maintaining GMP and data integrity compliance.
Location: Basel Stücki, Switzerland; work includes laboratory-based pharmaceutical development activities in Basel and Stein.
Company
is a life sciences company supporting customers in developing and manufacturing medicines across a globally connected network of sites.
What you will do
- Execute and report small-scale process development studies for parenteral products, including mixing hold time, VHP stress, filtration, filling behavior, and lyophilization.
- Support pharmaceutical development studies for liquid and lyophilized biologic drug products, including monoclonal antibodies, novel formats, ADCs, and peptides.
- Install, qualify, and maintain laboratory equipment and facilities in line with current practices and regulations.
- Implement and perform analytical tests such as HPLC, CE, UV content testing, pH, osmolality, and particle analysis.
- Prepare non-GMP drug product samples for stability studies and preclinical use using aseptic techniques.
- Document, interpret, and summarize results while following GMP, data integrity, health, and safety standards.
Requirements
- MSc in Pharmaceutical Sciences, Chemical Engineering, Biochemical Engineering, or a related discipline; laboratory technician training or equivalent experience may also be considered.
- Knowledge of fill-finish process steps for parenteral pharmaceutical products; experience in a pharmaceutical process development laboratory is advantageous.
- Strong reporting, scientific interpretation, and documentation skills.
- Good communication skills.
- Excellent written and spoken English is required.
Culture & Benefits
- 12-month fixed-term contract with full-time employment at 80–100%.
- Agile career opportunities and a dynamic work culture.
- Inclusive and ethical workplace.
- Performance-focused compensation programs.
- Collaborative environment focused on developing medicines and improving patient treatment.
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