Aktuelle Jobs im Zusammenhang mit Validation Specialist - Le Locle, Neuenburg - Randstad
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Validation Specialist
vor 3 Wochen
Le Locle, Neuenburg, Schweiz Randstad VollzeitJob Title: Validation SpecialistWe are seeking a skilled Validation Specialist to join our team at Randstad. As a Validation Specialist, you will be responsible for ensuring the quality and safety of medical devices by developing and executing validation protocols. Your primary goal will be to guarantee that our clients' products meet the highest standards...
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Validation Specialist
Vor 4 Tagen
Le Locle, Neuenburg, Schweiz Randstad VollzeitJob DescriptionWe are seeking a Validation Specialist for a dynamic and friendly working environment. This role is for an open-ended temporary contract. Fluency in French is required.Your ResponsibilitiesGeneration and execution of qualification/validation protocols, including documentation.Collaboration with project teams to develop a validation strategy...
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Validation Specialist
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Supplier Quality Assurance Specialist
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Supplier Quality Assurance Specialist
vor 4 Wochen
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Quality Assurance Specialist
vor 4 Wochen
Le Locle, Neuenburg, Schweiz Integra Lifesciences Switzerland SAS VollzeitJob Title: Supplier Quality EngineerAt Integra Lifesciences Switzerland SAS, we are committed to creating a better future for healthcare. As a Supplier Quality Engineer, you will play a crucial role in ensuring the quality and reliability of our products.Responsibilities:Lead the development and implementation of quality assurance strategies for contract...
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Supplier Quality Assurance Specialist
vor 4 Wochen
Le Locle, Neuenburg, Schweiz Integra Lifesciences Switzerland SAS VollzeitJob Title: Supplier Quality EngineerAt Integra Lifesciences Switzerland SAS, we are seeking a highly skilled Supplier Quality Engineer to join our team. As a key member of our quality assurance team, you will be responsible for ensuring the quality of our suppliers and contract manufacturers.Key Responsibilities:Lead supplier audits and assessments to ensure...
Validation Specialist
vor 2 Monaten
We are seeking a skilled Validation Engineer to join our team at Randstad. As a key member of our team, you will be responsible for ensuring the quality and compliance of our medical devices.
Key Responsibilities:
- Develop and execute qualification/validation protocols, including the generation and approval of summary documentation.
- Collaborate with project teams to develop validation strategies and statistically sound tests to support product testing.
- Complete test method validation, gauge R&R studies, and other qualifications or studies to support product testing.
- Schedule coordination, material allocation, and personnel alignment to successfully complete validation assignments.
- Develop statistically based sampling plans for in-process and final test sequencing.
- Ensure compliance with cGMP, cGLP, QSR, ISO, and other applicable requirements.
- Support and address comments and suggestions associated with validation and engineering documentation.
- Generate and approve protocol, deviation, and summary reports.
- Provide change control, non-conformance, and CAPA support.
Requirements:
- Bachelor's Degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry).
- 2 to 5 years of experience in a Validation or Quality Assurance role for a medical device or pharmaceutical environment.
- Fluency in French and good command of English.
- Excellent organizational and communication skills.
- Experience with qualifying medical devices, manufacturing equipment, or external components.
- Excellent technical writing skills with a thorough understanding of good documentation practice.
- Competent in tracking and updating schedules to provide upper management visibility of milestones and achievements.
- Proficient in Microsoft Office tools.
- Knowledge of statistical techniques.
