Packaging / Medical Device development Project Leader / no-841

Location
CH-Basel
Start
asap
End
12 months
Workload
100 %
All-in / Hour
rate: see job description
Total Hours
1920

Deadline:

Deadline
15.06.22

 

Packaging / Medical Device development Project Leader / no-841

Location
CH-Basel
Workload
100 %

Start

asap

End

12 months

DEADLINE

Deadline
15.06.22

  • CH-Basel
  • CH-Baselasap12 months100 % 1920rate: see job descriptionDeadline
    15.06.22

For our customer located in Basel/Switzerland we are currently looking for a: Packaging / Medical Device development Project Leader (m/f/x)

 

  • Gross rate Range (given by client): 55,77-62,74 chf/h gross

Tasks & Responsibilities

The successful candidate for this position will need to be able to lead the technical development of packaging and/or drug delivery systems within the Global Device & Packaging Development Department, from early phase activities up to commercialization and production scale up. In addition to outstanding project management and inter-personal skills, a strong technical background in medical devices and in pharmaceutical packaging development is crucial to support, monitor and challenge internal and external development partners.

 

Tasks and responsibilities would typically include:

 

  • Thorough project planning and execution
  • Leading the definition of product requirements for packaging, medical devices, delivery systems, e.g. drug/device combination products in which the device is generally already registered but sometimes to be developed
  • Leading the collaboration with external development partners:
    • Monitor work progress according to plan
    • Monitor, support and challenge technical development as well as test and verification work
    • Monitor development and implementation of manufacturing processes
  • Managing the collaboration with internal development partners and stakeholders
  • Provide primary packaging and device expertise in a broader cross-functional drug product development team
  • Evaluating and challenging technical solutions
  • Supporting and coordinating the manufacturing of clinical material and the production scale up
  • Supporting cross functional project teams in the development, review and submission of regulatory dossiers
  • Managing and monitoring Human Factors Engineering activities
  • Leading Risk management activities
  • Planning and monitoring of design verification activities (in-house)
  • Leading and authoring technical documentation
  • Ensuring a high quality Design History file
  • Transfer of Design History File to production

Must Haves

  • Bachelor’s or Master degree in Packaging Science/Engineering or Mechanical Engineering or University level Engineering education.
  • An ideal candidate would have a relevant degree in engineering and at least 7 years’ experience in leading device development technical teams in a similar area
  • Fluency in English language incl. technical writing.
  • Proficiency in German/French advantageous.
  • Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation)
  • Development and writing of technical documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects

 

Desired experience:

  • Good understanding of pharmaceutical development in general
  • Experience in project / program management of complex projects
  • Good experience of managing external suppliers
  • Mechanical engineering in general
    • Product design/Design for manufacture
    • Test and verification, incl. development of methods and equipment
  • General understanding of Human Factors Engineering, risk management and clinical studies processes and requirements
  •  Good communication and conflict solving skills

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Basel
  • CH-Baselasap12 months100 % 1920rate: see job descriptionDeadline
    15.06.22

For our customer located in Basel/Switzerland we are currently looking for a: Packaging / Medical Device development Project Leader (m/f/x)

 

  • Gross rate Range (given by client): 55,77-62,74 chf/h gross

Tasks & Responsibilities

The successful candidate for this position will need to be able to lead the technical development of packaging and/or drug delivery systems within the Global Device & Packaging Development Department, from early phase activities up to commercialization and production scale up. In addition to outstanding project management and inter-personal skills, a strong technical background in medical devices and in pharmaceutical packaging development is crucial to support, monitor and challenge internal and external development partners.

 

Tasks and responsibilities would typically include:

 

  • Thorough project planning and execution
  • Leading the definition of product requirements for packaging, medical devices, delivery systems, e.g. drug/device combination products in which the device is generally already registered but sometimes to be developed
  • Leading the collaboration with external development partners:
    • Monitor work progress according to plan
    • Monitor, support and challenge technical development as well as test and verification work
    • Monitor development and implementation of manufacturing processes
  • Managing the collaboration with internal development partners and stakeholders
  • Provide primary packaging and device expertise in a broader cross-functional drug product development team
  • Evaluating and challenging technical solutions
  • Supporting and coordinating the manufacturing of clinical material and the production scale up
  • Supporting cross functional project teams in the development, review and submission of regulatory dossiers
  • Managing and monitoring Human Factors Engineering activities
  • Leading Risk management activities
  • Planning and monitoring of design verification activities (in-house)
  • Leading and authoring technical documentation
  • Ensuring a high quality Design History file
  • Transfer of Design History File to production

Must Haves

  • Bachelor’s or Master degree in Packaging Science/Engineering or Mechanical Engineering or University level Engineering education.
  • An ideal candidate would have a relevant degree in engineering and at least 7 years’ experience in leading device development technical teams in a similar area
  • Fluency in English language incl. technical writing.
  • Proficiency in German/French advantageous.
  • Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation)
  • Development and writing of technical documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects

 

Desired experience:

  • Good understanding of pharmaceutical development in general
  • Experience in project / program management of complex projects
  • Good experience of managing external suppliers
  • Mechanical engineering in general
    • Product design/Design for manufacture
    • Test and verification, incl. development of methods and equipment
  • General understanding of Human Factors Engineering, risk management and clinical studies processes and requirements
  •  Good communication and conflict solving skills

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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