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Overarching Project Lead (all genders) - fulltime, permanent

AbbVie

Ludwigshafen am Rhein

Vor Ort

EUR 85.000 - 120.000

Vollzeit

Vor 13 Tagen

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Zusammenfassung

A leading pharmaceutical company in Ludwigshafen am Rhein seeks an Overarching Project Lead to lead a team of experts and develop global cross-functional strategies for drug product development. Candidates should have a PhD or comparable background, and at least 8 years of experience in parenteral Drug Products. This role involves managing teams, educating personnel on QbD approaches, and overseeing development initiatives while ensuring compliance with regulations. A flexible work model and a supportive environment are offered.

Leistungen

Attractive salary
Flexible work models
Comprehensive health programs
Mentorship during onboarding
Range of career opportunities

Qualifikationen

  • Pharmacist, Chemist, Biochemist, or Biologist with a comparable background required.
  • At least 8 years of experience in parenteral Drug Products.
  • Strong leadership skills and experience managing cross-functional teams.

Aufgaben

  • Lead the Overarching Project Group and develop global strategies.
  • Educate and train pharmaceutical personnel in QbD.
  • Manage global goals and initiatives to enhance parenteral development.

Kenntnisse

Leadership
Knowledge of regulations
QbD approaches
Collaboration

Ausbildung

PhD in relevant field
Jobbeschreibung

As Overarching Project Lead you are leading a group of highly skilled QRM experts and defining and aligning global cross-functional strategies regarding QbD and QRM development approaches. Furthermore your are representing the Drug Product (DP) team for a specific project and are responsible for activities related to drug product development and / or lifecycle management while considering legal requirements for pharmaceutical manufacturing in parenteral drug product development.

Your responsibilities are :

  • Leadership of Overarching Project Group within pPDS&T Drug Product Ludwigshafen including development and alignment of overarching development strategies as well as related framework and infrastructure in strong collaboration with partners and Representation of parenteral PDS&T organization in global project teams as DP Lead
  • Education and training of employees and pharmaceutical personnel in particular with regard to QbD approaches
  • Responsibility in developing globally aligned standardized QRM-based development approaches for parenterals in cross functional settings.
  • Development management and and guidance in the execution of global goals and initiatives to improve parenteral development and QbD strategies.
  • This includes the development of technical project plans and timelines aligned with quality risk management principles effective communication of project status and risks and clear appropriate presentation of data and strategies in alignment with regulatory expectations.
  • Creation and approval of GMP-compliant and regulatory documents (such as IMPD IND CTD for clinical trials and BLA NDA PAS for market submissions)

Qualifications :

This is how you make the difference :

  • You are a Pharmacist Chemist Biochemist Biologist or have a comparable background
  • You preferably have a PhD and at least 8 years of experience in relevant areas of parenteral Drug Products as well as a proven track‑record of advanced technical / scientific achievements
  • You possess the required knowledge of current regulations guidelines and the competitive landscape and are capable of working in a fast‑paced collaborative environment overseeing multiple projects and initiatives
  • Your strong leadership skills enable you to successfully manage cross‑functional teams and also act as direct people leader
  • You are experienced with QbD‑based development approaches

Zusätzliche Informationen :

Heres 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.

AbbVie setzt sich für Chancengleichheit ein und verpflichtet sich mit Integrität zu arbeiten Innovationen voranzutreiben Leben zu verändern und unserer Gemeinschaft zu dienen. Chancengleichheit bei Arbeitgeber / Veteranen / Behinderten.

Remote Work : No

Employment Type : Full‑time

Key Skills

Administrative Skills,Facilities Management,Biotechnology,Creative Production,Design And Estimation,Architecture

Experience : years

Vacancy : 1

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