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

Job title:

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

Company

Octapharma

Job description

Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.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) as Group Analytical Specialist QC (m/f/d) – Method Validation starting immediately.Ihre Aufgaben– 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

Ihr Profil

• 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

Wir bieten

• 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

Expected salary

Location

Wien

Job date

Thu, 28 Aug 2025 06:35:54 GMT

To help us track our recruitment effort, please indicate in your email/cover letter where (jobsjobs.org) you saw this job posting.