Vice Manager (m/f/d) Pharmaceutical Analytics

Date: May 5, 2022

Location: Hanau, HE, DE, 63450

Company: Heraeus

[title]
Vice Manager (m/f/d) Pharmaceutical Analytics
Location Hanau
Permanent 
Full Time
 

Imagine a job where you will have the opportunity to do exciting and challenging work while collaborating with extraordinary colleagues. A company that invests in you and your career, providing the training, mentoring, development, and support you need to be successful now and in the future. If you want a career without limits with a market-leading, family-owned, global company where you can make an impact, then imagine an opportunity at Heraeus. Every day, our worldwide team of around 14,800 employees brings forward new ideas and solutions that are impacting and transforming everything from healthcare and renewable energy to e-mobility, high-tech, and telecommunications.

 
 

The following Challenges await you:

  • In your role, you will work in the Quality Control (QC) department of the Pharmaceutical Ingredients business line and you will act as deputy head of QC.
  • You coordinate various projects within QC, such as the implementation of new software systems, e.g. a LIMS system, and take responsibility for the data integrity aspect, among others.
  • As part of the implementation of the LIMS system, you will set up and check master data and higher-level processes.
  • Your versatile activities include device and material qualifications, method validations as well as the creation and revision of standard operating procedures (SOP).
  • This also includes creating and reviewing validation protocols and validation reports, releasing analytical data as part of validation projects, and processing QABs and "out of specifications" (OOS). 
  • You will represent the QC Laboratory during customer audits and regulatory inspections and participate in GMP audits at external contract laboratories and internal interfaces.
  • Last but not least, you will be responsible for handling customer inquiries and staff qualifications/training.

 

Your Profile:

  • Academic scientific or technical education
  • Sound professional experience in the above-mentioned area of responsibility or in a comparable position
  • Very good knowledge in computer system validation (esp. LIMS) as well as in GMP (Good Manufacturing Practice)
  • Experience in project management desirable
  • Very good English, written and spoken
  • Resilient personality with an independent working style as well as customer- and solution-oriented action
  • Very good comprehension, analytical and strategic way of thinking and team spirit