Associate Director Quality & RP

We are growing, grow with us!

Are you looking for a dynamic company with new challenges and opportunities every day? Then this is your career opportunity. Our client works with the pharma, biotech and medtech industries, supporting businesses from early strategic planning and non-clinical requirements, through clinical development and regulatory submissions, to post-approval and post-marketing activities.

Our client is a leading global healthcare company with its roots in pharmaceutical distribution.

The success of their company grows with the excellent expertise and high motivation of their valued employees.

If your profession is not just a job, but also a mission and you enjoy working with people and in a team, then you are very welcome to apply.

We are looking for you to join our successful team with immediate effect as:

Associate Director - Quality Management & Compliance/Responsible Person for GDP

Your Job

You will take over consultancy activities for our clients in quality related projects, handling various tasks including but not limited to:

• Deliver high-quality services to our clients in the different QMC areas, including Auditing, Remediation, Quality Systems and Compliance, and expert Technical Consulting and Training
• Managing, implementing, and successfully executing projects, including time scheduling and budgeting and in compliance with applicable standards and adjustments of services if confirmed and required
• Support in obtaining an EU manufacturing authorization, commercialization readiness and market launch
• Assuming responsibility as a “Responsible Person” according to GDP regulations
• Delivery of GxP projects incl. int./ext. Training for manufacturing support
• Identify leads and opportunities within clients outside of the current project scope and partner with the Business Development and Sales team on scoping calls for new work and proposals as needed
• Collaborate with Project Operations to identify and build areas of efficiency

Develop and implement best practice opportunities to apply across all QMC service lines, and other affiliate offices as necessary

• Maintain contact with our clients and take over clients’ communication

Your Profile

• Master’s Degree in Life Science - Chemistry, pharmacy, biotechnology or similar
• 5+ years relevant work experience in the Life Sciences industry and/or within a consulting environment in the field of Quality Management & Compliance services
• Effectively resolving compliance issues
• Project Management experience/competency in cross functional int./ext. teams as well as strong technical writing skills
• Change-resilient, flexible and problem solving personality
• Very strong communication skills of written and spoken English, ideally also in German

​We off

erCollab

• oration in a motivated teamPlenty
• of room for creative ideas, personal responsibility and developmentFlexib
• le working hours and the option to work from homeCompan
• y bonusCompan
• y pension scheme with employer contributionHealth
• management (including free Gympass membership)Supple
• mentary company health insurance and travel health insurance
  
  If y

o

u

are interested in joining our clients team taking over this challenging job opportunity in our future-oriented company, we are looking forward to receive your CV stating your earliest possible starting date, any visa requirements.
Salar

y

in circa of €110k plus bonus to 10 %, pension, health & holiday entitlement!