Über AbbVie
AbbVie ist ein globales, forschendes BioPharma-Unternehmen. Unsere Mission ist es, innovative Therapien zu erforschen und bereitzustellen, um die medizinischen Herausforderungen von heute und morgen anzugehen. AbbVie will einen echten Unterschied im Leben der Menschen machen – über verschiedene Therapiegebiete hinweg: Immunologie, Onkologie, Neurologie, Augenheilkunde und Virologie sowie mit dem Portfolio von Allergan Aesthetics in der medizinischen Ästhetik. In Deutschland ist AbbVie an seinem Hauptsitz in Wiesbaden und seinem Forschungs- und Produktionsstandort in Ludwigshafen vertreten. Weitere Informationen findest du unter Folge @abbvie_de auf X oder besuche unsere Profile auf YouTube oder LinkedIn. Unter findest du umfangreiche Informationen zu den Therapiegebieten, in denen AbbVie tätig ist.
Job Description
The job that makes possibilities real in patients' lives. And yours.
The job that helps you get ahead in life. Moving mountains together.
Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!
Moving mountains together – as PostDoc - Assay Development Specialist for Novel Modalities (all genders) (full-time, temporary for 24 months)
The Program Manager, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for early phase (uncomplicated) compounds. The completion of clinical trials is the rate-limiting step for filing of new drug applications and, ultimately, to product commercialization. The on-time initiation, uninterrupted conduct, and completion of clinical studies is dependent on the timely delivery of clinical supplies of top quality to the clinical sites.
Responsibilities
* Develop complex bioanalytical methods to assess the pharmacokinetic properties and immunogenicity of various biologic therapeutic modalities (peptides, antibodies, antibody-drug conjugates, fusion proteins, gene- and cell therapies, siRNAs, etc.) in toxicokinetic and clinical trials, in accordance with international guidelines (e.g., FDA, EMA, ICH, OECD).
* Expand the existing method portfolio, including the implementation of new technologies, particularly in the peptide drug and cell and gene therapy area.
* Perform troubleshooting and engage in scientific discussions to develop solution strategies for complex analytical problems.
* Collaborate with international multidisciplinary teams to advance project goals.
* Prepare and maintain GLP/GCP-compliant documentation
Qualifications
Qualifications
* Ph.D. in Biochemistry or a related scientific discipline.
* Relevant experience in establishing complex bioanalytical methods for various biological modalities
* Strong expertise in protein biochemistry and bioanalytical techniques, eg. ligand-binding assays
* Cell culture expertise and experience with the automation of bioanalytical methods are desirable.
* Excellent ability to critically evaluate existing methods and guidelines and develop innovative solutions.
* Proficiency in spoken and written English
* Strong computer skills.
* Knowledge of bioanalytically relevant regulations (FDA, EMA, ICH, OECD) and experience working under GxP quality standards are desirable.
Here's how we can move mountains together
* with a diverse work environment where you can have a real impact
* with an open corporate culture
* with an attractive salary
* with an intensive onboarding process with a mentor at your side
* with flexible work models for a healthy work-life balance
* with a corporate health management that offers comprehensive health and exercise programs
* with company social benefits
* with a wide range of career opportunities in an international organization
* with top-tier, attractive development opportunities
* with a strong international network
Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.
Have questions? Email TalentAcquisition.de@abbvie.com– We look forward to hearing from you!
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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