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16238en
- Contract
- English
- Not Applicable*
- Digital & Technology
- Bern
- Healthcare & Life Sciences
Skills
2-3 years of experience; knowledge of quality management systems and regulatory standards; experience with test methods, design control, and risk management.
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We are seeking a Packaging and Device Engineer to join our client in the pharmaceutical industry. You will help develop and improve packaging materials, medical devices, and combination products in this role. You will work with teams across the company, such as Regulatory, Quality Assurance, Production, and Supply Chain, to ensure products meet quality and compliance standards.
Key Responsibilities:
- Select, assess, and implement new and existing packaging materials and devices.
- Support the design and maintenance of released products and manage product updates and improvements.
- Collaborate with different teams to address product complaints, perform root cause analysis, and ensure compliance.
- Ensure all designs meet regulatory standards and quality requirements (ISO 13485, 21CFR820, ISO14971).
- Build and manage relationships with suppliers and external partners.
- Develop plans for Human Factors Engineering and write study protocols.
Requirements:
- Degree in engineering, biotechnology, or a related field.
- At least 5 years of experience in pharmaceutical device development.
- Knowledge of quality management systems and regulatory standards.
- Experience with test methods, design control, and risk management.
This is an 11-month contract, and they are seeking someone who can start as soon as possible.
Key Responsibilities:
- Select, assess, and implement new and existing packaging materials and devices.
- Support the design and maintenance of released products and manage product updates and improvements.
- Collaborate with different teams to address product complaints, perform root cause analysis, and ensure compliance.
- Ensure all designs meet regulatory standards and quality requirements (ISO 13485, 21CFR820, ISO14971).
- Build and manage relationships with suppliers and external partners.
- Develop plans for Human Factors Engineering and write study protocols.
Requirements:
- Degree in engineering, biotechnology, or a related field.
- At least 5 years of experience in pharmaceutical device development.
- Knowledge of quality management systems and regulatory standards.
- Experience with test methods, design control, and risk management.
This is an 11-month contract, and they are seeking someone who can start as soon as possible.
I manage this role