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Analytical Project Leader, 100%

Corden Pharma Switzerland LLC

Employment type
Full-time
Location
Liestal
Company
Corden Pharma Switzerland LLC, Eichenweg 1, 4410 Liestal
First posted
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Analytical Project Leader (APL), 100% (m/w/d) CordenPharma is a leading provider for the development and manufacture of active pharmaceutical ingredients (APIs), excipients, finished dosage forms, and packaging activities with more than 2,600 employees worldwide. With our services, we support pharma and biotech companies in the manufacture of medicines with the primary goal of improving people's lives. Our network in Europe and the USA offers flexible and specialized solutions on five technology platforms: Peptides, Lipids & Carbohydrates, Injectable, Highly Potent & Oncology; and Small Molecules. We are committed to delivering the highest quality in all these areas for the benefit of patients. At the earliest possible date, we are looking for at the Liestal location a/an Analytical Project Leader (APL), 100% (m/w/d) Liestal by arrangement Full-time permanent Your exciting area of responsibility You are the central single point of contact (SPOC) for all analytical work packages in development and production projects for the manufacture of APIs and excipients and ensure their timely, quality, and budget-compliant implementation for our customers. You are responsible for and lead all analytical activities, such as method development, validations, and troubleshooting, across all project phases (Early to Late Stage). In doing so, you bring your expertise at the API location Liestal particularly in the areas of peptides, lipids, and small molecules. You plan, coordinate, and prioritize the analytical work packages in close cooperation with internal and external stakeholders. You monitor the project progress, report regularly to stakeholders, and initiate appropriate measures for complex analytical issues. You assume technical responsibility for the analytical project team, e.g., analytical experts and analytical scientists, in a matrix organization. Responsibility for the analytical contribution within the framework of project evaluations. Creation, revision, and review of GMP-relevant project documents (plans, reports, methods). You create and check SOPs in your area of responsibility and ensure their technical currency and regulatory compliance. You ensure that analytical SOPs and processes always comply with current regulatory requirements. You drive the further development of analytical processes, documentation, and tools and support the establishment of modern methodical and procedural standards in the field of analytics. You coach APL colleagues, support recruitment and the induction of new employees, and promote the further development of analytical competencies within the team. Your profile Completed studies in analytical chemistry, pharmacy, or a comparable natural science field Several years of experience in analytical project management across several development phases (Early to Late Stage), ideally with customer contact Sound knowledge in instrumental analysis (e.g., HPLC, GC, MS) as well as experience with peptides, lipids, and small molecules are an advantage Confident handling of cGMP and regulatory requirements Very good communication skills and confidence in dealing with complex analytical issues Independent, structured, and customer-oriented way of working as well as high reliability and ability to work in a team Very good German as well as good English skills in speaking and writing. What we offer you Dynamic and exciting working environment An attractive workplace with a high level of responsibility Corden Pharma offers you interesting and diverse tasks in a highly motivated team. Through practical induction, we help you to gain technical security in order to be able to work independently with a high level of personal responsibility. Could this fit? If you enjoy working in a team and it is a matter of course for you to think and act beyond your own area, then you have come to the right place! We look forward to your application documents. Städtler Director, Head of Human Resources jpidc7aef61jm jit0727jm jiy26jm

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