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- Aufgaben: Lead analytical projects and collaborate with cross-functional teams in drug development.
- Arbeitgeber: Join a cutting-edge pharmaceutical company focused on innovative drug manufacturing.
- Mitarbeitervorteile: Enjoy a dynamic work environment with opportunities for professional growth and collaboration.
- Warum dieser Job: Be part of impactful projects that contribute to life-saving medications and clinical trials.
- Gewünschte Qualifikationen: Master's or Ph.D. in relevant fields with 3+ years in the pharmaceutical industry required.
- Andere Informationen: Position based in Basel, project planned until 2028.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
Analytical Project Leader Scientist (m/f/d) – 100%
This position is located in Analytical Development Synthetic Molecules within Pharma Technical Development. Analytical Development is responsible for the development of resource and cost-efficient analytical methods for all materials used during drug manufacturing using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas Chromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of their work is a robust control strategy to release pharmaceutical products for clinical trials, and finally for commercial supply.
Tasks and responsibilities
- Cover all analytical aspects during the project development lifecycle
- Work in close collaboration with peers, lab technicians and cross-functional partners from e.g. process development, material sciences, manufacturing, regulatory affairs, and quality assurance
- Plan and document experiments/results independently, and prepare for regulatory submissions such as IND (Investigational New Drug) and NDA (New Drug Application)
- Be part of larger Technical Development Teams in which you regularly report out your progress
- Collaborate with stakeholders from different disciplines, varying with the clinical phase of the project
- Network closely with external partners such as CMOs and CROs
Main requirements
- Master or Ph.D. in chemistry, pharmacy, biotechnology or biochemistry
- Minimum 3 years professional experience in the pharmaceutical industry
- Experience in analytical development with Oligonucleotides, Peptides, biologically derived molecules and their advanced formulations is a plus
- Knowledge in analytical methodologies such as e.g. PCR sequencing is a plus
- Strong quality mind-set and excellent attention to detail
- Experience in applying GMP requirements where necessary, understanding how to exert them in different clinical phases
- Ideally experience of working in a paperless environment with strong IT skills to support digital transformation initiatives
- Open-minded, goal-oriented, and able to work in a fast-developing environment
- Takes challenges as opportunities and ability to respectfully collaborate with team members, customers and stakeholders
- Fluent in English, German is a plus
General information
- Planned duration: project planned until 2028
- Workplace: Basel
If you are interested in this position, please send your CV in English.
Seniority level
- Associate
Employment type
- Temporary
Job function
- Science
Industries
- Pharmaceutical Manufacturing and Research Services
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Wissenschaftler:in Arbeitgeber: Gi Group
Kontaktperson:
Gi Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Wissenschaftler:in
✨Tip Number 1
Make sure to highlight your experience with analytical methodologies like HPLC, GC, and MS during networking opportunities. Engaging in discussions about these techniques can showcase your expertise and make you stand out.
✨Tip Number 2
Connect with professionals in the pharmaceutical industry through platforms like LinkedIn. Join relevant groups and participate in discussions to increase your visibility and learn more about the latest trends in analytical development.
✨Tip Number 3
Consider attending industry conferences or workshops focused on pharmaceutical development. These events are great for networking and can provide insights into the skills and knowledge that are currently in demand.
✨Tip Number 4
Familiarize yourself with regulatory submissions like IND and NDA. Understanding these processes will not only prepare you for the role but also demonstrate your commitment to the field during interviews.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Wissenschaftler:in
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Analytical Project Leader Scientist position. Understand the key responsibilities and requirements, especially the analytical methodologies mentioned, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your professional experience in the pharmaceutical industry, particularly in analytical development. Mention any specific projects or methodologies you've worked with that align with the job requirements.
Showcase Your Skills: Clearly outline your skills related to analytical methods such as HPLC, GC, and MS. If you have experience with Oligonucleotides or Peptides, make sure to highlight this, as it is considered a plus for the role.
Prepare Your Application in English: Since the job requires submitting your CV in English, ensure that your application documents are well-written and free of errors. Use clear and concise language to convey your qualifications and enthusiasm for the position.
Wie du dich auf ein Vorstellungsgespräch bei Gi Group vorbereitest
✨Showcase Your Analytical Skills
Be prepared to discuss your experience with analytical methodologies like HPLC, GC, and MS. Highlight specific projects where you successfully developed or implemented these techniques.
✨Demonstrate Collaboration Experience
Since the role involves working closely with cross-functional teams, share examples of how you've effectively collaborated with peers from different disciplines in past projects.
✨Prepare for Regulatory Discussions
Familiarize yourself with the regulatory submission processes such as IND and NDA. Be ready to discuss your experience in planning and documenting experiments that align with these requirements.
✨Emphasize Your Quality Mindset
Discuss your attention to detail and how you apply GMP requirements in your work. Provide examples of how you ensure quality in your analytical development processes.
