Group Analytical Specialist QC (m/f/d) - Method Validation

Group Analytical Specialist QC (m/f/d) – Method Validation

Octapharma is a global company whose products support patients in 118 countries worldwide. Our medicines are high-quality human proteins extracted from human plasma and human cell lines.
Octapharma Produktionsgesellschaft Deutschland mbH (OPGD) in Springe near Hanover is one of five state-of-the-art production sites. There, our approximately 800 employees manufacture the finished medicinal product albunorm as well as intermediate products for further processing.

We look forward to continuing our growth together with you (m/f/d) asGroup Analytical Specialist QC (m/f/d) – Method Validation starting immediately.

What is the best thing about working with us?

• You help save lives – every day is meaningful because we manufacture life-saving medicines
• Social benefits – employer-funded company pension scheme, Hansefit, benefits portal with advantageous offers, bicycle leasing, external health coaching and regular company parties
• Skills development – We offer various internal and external employee and management training courses, trainee programmes and digital solutions
• With us, you can start your weekend early with a short Friday

What are your responsibilities as Group Analytical Specialist QC (m/f/d) – Method Validation?

• Prepare validation documents and other GMP-relevant documents with the support of senior analyticalspecialists and team leaders
• Develop and validate methods
• Support troubleshooting in the QC laboratories
• Manage sample administration and follow-up of validation-related testing in the QC and R&D laboratories
• Support method transfer and the issue/update of product specifications
• Administer documents required for submission and assist with inspection tasks
• Prepare statistical evaluations of data and reports using Excel

Your profile that will convince us:

• University degree (MSc, PhD, or equivalent) in Chemistry or Biosciences
• Work experience in the pharmaceutical industry, especially in the field of method validation (GMPenvironment), is a plus
• Willingness to travel for business (approx. 5% per year, domestically and internationally)
• Good knowledge of MS Word and MS Excel
• English communication skills (oral and written)
• Strong social and presentation skills
• Strong problem-solving, organizational, and time-management skills. Ability to multitask and a high level offlexibility

Apply now!

Nils Krummland (HR Business Partner) looks forward to receiving your application, including details of your availability and salary expectations, via our career portal.

Find out more about the Springe location on our website and follow us onLinkedIn !

#J-18808-Ljbffr