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- Aufgaben: Supervise compliance and manage Quality Agreements for drug production.
- Arbeitgeber: Join a leading pharmaceutical company in Visp, Switzerland.
- Mitarbeitervorteile: Gain experience in a dynamic environment with opportunities for professional growth.
- Warum dieser Job: Be part of a team that ensures high-quality standards in drug production.
- Gewünschte Qualifikationen: Bachelor's or Master’s in Life Sciences; 5-10 years in Quality Assurance required.
- Andere Informationen: Fluency in English is mandatory; German is a plus.
Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.
Location: Visp, Switzerland
Contract: Until end of the year
Languages: English (mandatory), German (a clear asset)
Job Overview:
We are seeking a highly skilled and experienced professional to supervise compliance and customer Quality Agreement (QAA) activities for drug production. This role requires close collaboration with Drug Product Services (DPS) in Basel/Stein sites (e.g., Slough/Visp) to establish and negotiate Quality Agreements.
Key Responsibilities:
- Establish, negotiate, and maintain Quality Agreements (QAA) in collaboration with DPS and DS sites.
- Act as the primary point of contact for Drug Product QA-related inquiries, topics, and customer complaints.
- Support and manage interactions in cases of changes, deviations, technical complaints, out-of-specification results, and other quality-related matters.
- Represent Quality Assurance in cross-functional teams and maintain interfaces with Manufacturing, QC, Support Functions, Project and Site Engineering for effective task execution.
- Serve as the QA representative in project teams and customer meetings during technical transfers.
- Act as the QA contact for specific projects, ensuring regular follow-ups on DR and CR with customers.
- Support and approve project/product-specific risk assessments, regulatory gap analyses, and risk evaluations.
- Review and release product-specific documentation, including process descriptions, workflows, recipes, manufacturing protocols, transfer documents, test plans, and parameter lists.
- Work closely with QC-Project Leaders (QC-PL) and MSAT for New Product Introductions (NPI).
- Assess, review, and approve quality records such as deviations, change control, CAPAs, investigations, effectiveness checks, and extensions in compliance with local SOPs.
- Author, review, and approve GMP-relevant documents and SOPs.
- Support continuous improvement programs to enhance the Quality Management System for Drug Product.
Qualifications & Experience:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
- 5-10 years of relevant experience in Quality Assurance within drug production or pharmaceutical manufacturing.
- Strong knowledge of GMP regulations and compliance requirements.
- Experience in negotiating and managing Quality Agreements with external partners.
- Ability to assess and resolve quality-related issues, including deviations, complaints, and investigations.
- Proven ability to work cross-functionally with Manufacturing, QC, Engineering, and Regulatory teams.
- Excellent communication and stakeholder management skills.
- Proficiency in English is mandatory; German is a strong asset.
If you are a detail-oriented QA professional with a strong background in compliance and quality agreements, we encourage you to apply and be part of our growing team!
Interested? Send your CV to Daria at or call +41445514407 for more info.
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QA PL Drug Product Arbeitgeber: Panda International
Kontaktperson:
Panda International HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: QA PL Drug Product
✨Tip Number 1
Familiarize yourself with the specific Quality Agreements (QAA) that are commonly used in the pharmaceutical industry. Understanding the nuances of these agreements will help you demonstrate your expertise during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, especially those involved in Quality Assurance. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Brush up on your knowledge of GMP regulations and compliance requirements. Being able to discuss these topics confidently will show your preparedness for the role.
✨Tip Number 4
If you speak German, make sure to highlight this skill during your interactions. It’s a strong asset for this position and can set you apart from other candidates.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: QA PL Drug Product
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the QA PL Drug Product position. Understand the key responsibilities and qualifications required, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 5-10 years of experience in Quality Assurance within drug production or pharmaceutical manufacturing. Be specific about your achievements and how they relate to the responsibilities outlined in the job description.
Showcase Language Skills: Since proficiency in English is mandatory and German is a strong asset, make sure to clearly state your language skills in your application. If you have certifications or relevant experiences that demonstrate your language abilities, include those as well.
Tailor Your Application: Customize your CV and cover letter to reflect the specific requirements of the job. Use keywords from the job description, such as 'Quality Agreements', 'GMP regulations', and 'cross-functional teams', to show that you are a perfect fit for the role.
Wie du dich auf ein Vorstellungsgespräch bei Panda International vorbereitest
✨Showcase Your Experience
Be prepared to discuss your 5-10 years of relevant experience in Quality Assurance. Highlight specific examples where you successfully managed Quality Agreements or resolved quality-related issues.
✨Demonstrate Cross-Functional Collaboration
Since this role requires working closely with various teams, share instances where you've effectively collaborated with Manufacturing, QC, and Engineering teams. This will show your ability to work cross-functionally.
✨Understand GMP Regulations
Brush up on your knowledge of GMP regulations and compliance requirements. Be ready to discuss how you've applied these in your previous roles, as this is crucial for the position.
✨Prepare for Language Proficiency
Since proficiency in English is mandatory and German is a strong asset, practice discussing your experiences in both languages. This will demonstrate your communication skills and readiness for the role.
