AbbVie Senior Scientist - Process Engineering Late Stage Drug Product Development (m/w/d) - (unbefristet / Vollzeit) in Ludwigshafen, Germany
AbbVies Mission ist es innovative Medikamente zu entdecken, die im Heute schwerwiegende Gesundheitsprobleme lösen und die medizinischen Herausforderungen von morgen angehen. Wir streben danach, in verschiedensten therapeutischen Schlüsselbereichen einen bemerkenswerten Einfluss auf das Leben der Menschen auszuüben: Immunologie, Onkologie, Neurowissenschaften, Augenheilkunde, Virologie, Frauengesundheit und Gastroenterologie sowie Produkte und Dienstleistungen aus dem gesamten Portfolio von AbbVie im Bereich der Allergan-Aesthetics. Für weitere Informationen über AbbVie besuchen Sie uns bitte unter www.abbvie.com . Folgen Sie @abbvie auf Twitter (https://twitter.com/abbvie) , Facebook (https://www.facebook.com/AbbVieGlobal) , Instagram (https://www.instagram.com/abbvie/?hl=en) , YouTube (https://www.youtube.com/user/AbbVie) und LinkedIn (https://www.linkedin.com/company/abbvie) .
Execute and lead late-stage drug product development projects. Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.
Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.
Willingness to travel to other AbbVie sites and third-party manufacturers to support and facilitate late-stage drug product projects and the technical transfer to Operations
Demonstrate the ability to lead late-stage development projects in CMC environment
Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
Publish research in peer-reviewed journals and present work at scientific conferences.
Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program.
Seize opportunities to pursue project relevant leads that are in line with the group’s strategy.
Maintain a high level of productivity in the lab.
Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.
You hold a Bachelor’s Degreeor equivalent education and typically 12 years of experience, Master’s degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience.
You are an effective writer and communicator of internal reports, external research, or other regulatory materials.
You have experience from previous positions in industry, especially around scale-up, technical transfer and data automation.
You are able to work in a structured manner and fully independent.
You are open to working effectively with people from all parts of the world.
Fluent English and German language
Ja, 10 % der Zeit
Job Level Code
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.