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- Aufgaben: Supervise quality agreements and manage customer interactions for Drug Product.
- Arbeitgeber: Join a leading company in chemical manufacturing with a focus on quality assurance.
- Mitarbeitervorteile: Full-time position with potential for extension and a collaborative work environment.
- Warum dieser Job: Be part of cross-functional teams and contribute to impactful quality management initiatives.
- Gewünschte Qualifikationen: 5-10 years of experience; fluent in English, German is a plus.
- Andere Informationen: Position based in Visp, with a contract until 31/12/2025.
Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.
For a company we are looking for a
QA PL Drug Product (m/f/d) – 100%
Tasks and responsibilities
- Supervise Compliance & Customer quality agreement (QAA) activities for Drug Product Visp.
- Establish and negotiate Quality Agreements (QAA) in close collaboration with Drug Product Services DPS in Basel / Stein and LONZA Drug Substance (DS) sites (e.g. Slough / Visp).
- Act as point of contact for Drug Product QA related questions, topics and complaints from customers related to the manufacturing operations. Support and manage interactions in cases of changes, deviations, technical complaints, out of specification results and others.
- Represent Quality Assurance in cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project- and Site Engineering project / technology transfer to effectively execute tasks related to Drug Product processes.
- Act as QA representative in Project teams and represent QA in customer meetings during Technical Transfer.
- Act as QA contact for specific projects and realize the interface for DR and CR with the customer (routine follow-up’s).
- Support and approve project / product specific risk assessments or regulatory specific risk or gap assessments.
- Review and release product specific documentation such as process descriptions and workflows, recipes, manufacturing protocols, transfer documents, test plans, parameter lists, etc.
- Work closely with QC-Project Leader (QC-PL) and MSAT for New-Product-Introductions (NPI).
- Assess, review and approve quality records e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions in line with current local SOPs.
- Author, review and approve GMP-relevant documents and SOPs.
- Support continuous improvement programs to establish an effective Quality Management System for Drug Product.
- Support and approve project / product specific risk assessments.
Your profile
- Work experience 5- 10 years
- Fluent in English, German is a plus
General information
- Duration of employment: 31/12/2025 (with possible extension)
- Place of work: Visp
Your application
If you are interested in this opportunity, please send your CV in English to:
Work: +41 76 349 92 60
Seniority level
- Associate
Employment type
- Full-time
Job function
- Other
- Chemical Manufacturing
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QA PL Drug Product (m/f/d) - 100% Arbeitgeber: Gi Group
Kontaktperson:
Gi Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: QA PL Drug Product (m/f/d) - 100%
✨Tip Number 1
Make sure to familiarize yourself with the specific Quality Agreements (QAA) relevant to Drug Products. Understanding these agreements will help you demonstrate your expertise during interviews and show that you can effectively negotiate and establish quality standards.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in QA roles. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations, which can be beneficial when discussing your fit for the role.
✨Tip Number 3
Prepare to discuss your experience with cross-functional teams and how you've successfully managed interactions during technical transfers or project implementations. Highlighting these experiences will showcase your ability to collaborate effectively in a complex environment.
✨Tip Number 4
Stay updated on current trends and regulations in Quality Assurance within the pharmaceutical sector. Being knowledgeable about recent changes can give you an edge in discussions and demonstrate your commitment to continuous improvement in quality management systems.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: QA PL Drug Product (m/f/d) - 100%
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the QA PL Drug Product position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 5-10 years of relevant work experience in quality assurance, particularly in drug product processes. Use specific examples that demonstrate your expertise in compliance, quality agreements, and project management.
Showcase Language Skills: Since fluency in English is required and German is a plus, make sure to clearly state your language proficiency in your application. If you have certifications or relevant experiences, include those as well.
Tailor Your Documents: Customize your CV and cover letter to reflect the specific requirements of the job. Use keywords from the job description to ensure your application stands out and aligns with what the company is looking for.
Wie du dich auf ein Vorstellungsgespräch bei Gi Group vorbereitest
✨Understand Quality Agreements
Make sure you have a solid grasp of what Quality Agreements (QAA) entail. Be prepared to discuss your experience in establishing and negotiating these agreements, as well as how you've collaborated with different teams in the past.
✨Showcase Your Problem-Solving Skills
Be ready to provide examples of how you've managed deviations, technical complaints, or out-of-specification results. Highlight your approach to resolving these issues and how you ensure compliance with quality standards.
✨Highlight Cross-Functional Collaboration
Since the role involves working with various teams, emphasize your experience in cross-functional collaboration. Discuss specific projects where you acted as a liaison between QA and other departments, showcasing your communication skills.
✨Prepare for Technical Questions
Expect technical questions related to quality management systems and GMP-relevant documents. Brush up on your knowledge of risk assessments, CAPAs, and SOPs, and be ready to discuss how you've applied these in your previous roles.
