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- Aufgaben: Lead quality projects, analyze data, and support audits in a biotech environment.
- Arbeitgeber: Join Octapharma, a leading global biopharmaceutical company focused on innovative human protein therapies.
- Mitarbeitervorteile: Enjoy flexible hours, 30 vacation days, training opportunities, and a subsidized company restaurant.
- Warum dieser Job: Be part of a growing team making a real impact in patient care with cutting-edge technology.
- Gewünschte Qualifikationen: Degree in natural sciences and 3+ years in GMP; project management skills are a plus.
- Andere Informationen: Work in an international team with a modern workspace in Heidelberg.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
Job Description
Octapharma Biopharmaceuticals GmbH
a subsidiary of the Octapharma group founded in 1997 is a successful and expanding biotech company in Heidelberg. Our core business is the development of recombinant proteins produced in human cell lines for therapeutic use in humans. We strive for effective treatments with an improved tolerability and convenience for our patients.\\nWe are looking for a Project Manager Quality (m/f/d) at our site in Heidelberg for the next possible date.\\nProject Manager Quality (m/f/d)\\nWhat will you be doing as Project Manager Quality?
Lead and support of quality related projects\\nCompiling and reporting of project related data and documents\\nCompiling, analyzing and presenting KCIs related to processes\\nFallow up on change controls in TW related to quality related projects\\nSupport other departments regarding different topics and projects (improvement of existing quality systems, implementation of new quality systems, QAAs and supplier overview etc.)\\nSupport for audit/inspection preparation and inspection readiness
Who are you?
Successfully completed studies in natural sciences (e.g. biochemistry, biology, biotechnology, chemistry, pharmacy)\\nKnowledge of project management tools and experience in project leading\\nGood GMP knowledge (e.g. US-FDA, EU directives and guidelines, ICH, AMG, AMWHV) and at least three years of professional experience in the GMP environment\\nPersonal responsibility, resilience, team spirit and analytical thinking\\nPrecise and structured way of working\\nGood knowledge of German and English\\nGood computer skills and knowledge in MS Office
What’s the best thing about working with us?
A permanent position in full-time (40 hrs./week) in a constantly growing company\\nA modern, "state of the art" working environment\\nFlexible working hours\\nRegular opportunities for further training\\n30 days vacation\\nOwn company restaurant with subsidies\\nFree drinks such as coffee, tea and water\\nJob ticket or parking space for bicycle or car\\nAn international team in an international corporate environment\\nA collegial environment with many opportunities for activities\\nAbout Octapharma\\nHeadquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines.\\nOctapharma employs nearly 12,000 people worldwide to support the treatment of patients in 118 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care.\\nOctapharma has seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany and Sweden, and operates more than 195 plasma donation centres across Europe and the US. Octapharma has 40 years of experience in patient care.\\nFor more information, please visit
www.octapharma.com\\nApply Today!
Please apply via our web portal only. (reference number
59396 )
Contact person:\\nDorothee Schaupp – Human Resources\\nTel: +49 (0)6221 – 1852 546\\nwww.octapharma.com
Project Manager Quality (m/f/d) Arbeitgeber: Octapharma Biopharmaceuticals GmbH
Kontaktperson:
Octapharma Biopharmaceuticals GmbH HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Project Manager Quality (m/f/d)
✨Tip Number 1
Make sure to familiarize yourself with the specific GMP regulations and guidelines relevant to the biopharmaceutical industry. Understanding the nuances of US-FDA, EU directives, and ICH guidelines will give you a significant edge during the interview process.
✨Tip Number 2
Highlight your experience with project management tools in your discussions. Be prepared to share specific examples of how you've successfully led quality-related projects in the past, as this will demonstrate your capability to handle the responsibilities of the role.
✨Tip Number 3
Showcase your analytical thinking skills by discussing how you've approached problem-solving in previous roles. Providing concrete examples of how you've improved quality systems or handled audits can set you apart from other candidates.
✨Tip Number 4
Since the role requires good knowledge of both German and English, practice discussing technical topics in both languages. This will not only boost your confidence but also demonstrate your communication skills during the interview.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Project Manager Quality (m/f/d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Project Manager Quality at Octapharma. Highlight your relevant experience in quality-related projects and your knowledge of GMP regulations in your application.
Tailor Your CV: Customize your CV to reflect your background in natural sciences and project management. Emphasize your experience with GMP guidelines and any specific tools or methodologies you have used in previous roles.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your skills and experiences to the job description. Mention your analytical thinking, team spirit, and how you can contribute to improving quality systems at Octapharma.
Proofread Your Application: Before submitting, carefully proofread your application for any errors in spelling or grammar. Ensure that your documents are well-structured and clearly present your qualifications and motivation for the role.
Wie du dich auf ein Vorstellungsgespräch bei Octapharma Biopharmaceuticals GmbH vorbereitest
✨Understand GMP Regulations
Make sure you have a solid grasp of Good Manufacturing Practices (GMP) and relevant regulations like US-FDA and EU directives. Be prepared to discuss how your experience aligns with these standards.
✨Showcase Project Management Skills
Highlight your experience with project management tools and methodologies. Be ready to provide examples of projects you've led, focusing on your role in quality-related initiatives.
✨Demonstrate Analytical Thinking
Prepare to discuss how you approach problem-solving and data analysis. Use specific examples to illustrate your analytical skills and how they have contributed to successful project outcomes.
✨Communicate Effectively in Both Languages
Since the role requires good knowledge of both German and English, practice discussing your qualifications and experiences in both languages. This will show your versatility and readiness for an international team environment.
