FPL Support – Formulation Manufacturing Project Leader / no-167

Location
CH-Basel
Start
01/11/2021
End
31/10/2022
Workload
100 %
All-in / Hour
please ask us for more details
Total Hours
2.088

Deadline:

 

FPL Support – Formulation Manufacturing Project Leader / no-167

Location
CH-Basel
Workload
100 %

Start

01/11/2021

End

31/10/2022

DEADLINE

  • CH-Basel
  • CH-Basel01/11/202131/10/2022100 % 2.088please ask us for more details

For our customer located in Basel/Switzerland we are currently looking for a:  FPL Support (m/f/d)

  • Location: Basel
  • Branch: Pharma
  • Duration: 12 months 

Tasks & Responsibilities

Job purpose to support drug product manufacturing process related development and supply activities for parenteral and ocular small molecule drug products in Post POC phase. This includes the scientific evaluation and presentation of data, authoring of technical and GMP documentation, integrity checks against raw data and on-site manufacturing support to technical and clinical manufacturing campaigns. You work in a cross-functional team with manufacturing operations, analytics and QA and contribute to the overall Technical Research and Development strategies and goals. You work under minimal guidance of more experienced formulation project leaders.

  • support drug product formulation development and manufacturing activities at internal or external manufacturing sites for assigned projects in line with the project plan, guidelines and procedures
  • collaborate with operational colleagues working on your process at the respective manufacturing sites
  • take accountability for formulation and manufacturing process deliverables incl. GMP related aspects and change control
  • author manufacturing instructions for clinical manufacturing campaigns, compile data and interpret results, evaluate data, draw relevant conclusions and contribute to development reports and Quality risk assessment documents in close collaboration with the project teams
  • perform document reviews and data integrity checks against raw data
  • support deviation investigations and drive change control
  • exchange regularly within your project team as well as seek guidance with internal experts on diverse aspects

Must Haves

  • Master degree or higher in life sciences, ideally in the Pharmaceutical field
  • Ideally more than 5 years industrial experience in the development and / or clinical manufacturing of pharmaceutical formulations for small molecules and with experience in late phase development and launch activities.
  • Experience in ocular or parenteral development preferable.
  • Interdisciplinary thinking and interest in collaboration with other functions
  • Good knowledge of GMP and GLP
  • Good knowledge of ocular and/or parenteral dosage form technologies and laboratory and/or technical tools
  • Good scientific / technical writing skills
  • Good collaboration skills and team spirit enabling you to work in a matrix environment, good communication and negotiation skills
  • Fluent in English (oral and written), German is an advantage

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-Basel01/11/202131/10/2022100 % 2.088please ask us for more details

For our customer located in Basel/Switzerland we are currently looking for a:  FPL Support (m/f/d)

  • Location: Basel
  • Branch: Pharma
  • Duration: 12 months 

Tasks & Responsibilities

Job purpose to support drug product manufacturing process related development and supply activities for parenteral and ocular small molecule drug products in Post POC phase. This includes the scientific evaluation and presentation of data, authoring of technical and GMP documentation, integrity checks against raw data and on-site manufacturing support to technical and clinical manufacturing campaigns. You work in a cross-functional team with manufacturing operations, analytics and QA and contribute to the overall Technical Research and Development strategies and goals. You work under minimal guidance of more experienced formulation project leaders.

  • support drug product formulation development and manufacturing activities at internal or external manufacturing sites for assigned projects in line with the project plan, guidelines and procedures
  • collaborate with operational colleagues working on your process at the respective manufacturing sites
  • take accountability for formulation and manufacturing process deliverables incl. GMP related aspects and change control
  • author manufacturing instructions for clinical manufacturing campaigns, compile data and interpret results, evaluate data, draw relevant conclusions and contribute to development reports and Quality risk assessment documents in close collaboration with the project teams
  • perform document reviews and data integrity checks against raw data
  • support deviation investigations and drive change control
  • exchange regularly within your project team as well as seek guidance with internal experts on diverse aspects

Must Haves

  • Master degree or higher in life sciences, ideally in the Pharmaceutical field
  • Ideally more than 5 years industrial experience in the development and / or clinical manufacturing of pharmaceutical formulations for small molecules and with experience in late phase development and launch activities.
  • Experience in ocular or parenteral development preferable.
  • Interdisciplinary thinking and interest in collaboration with other functions
  • Good knowledge of GMP and GLP
  • Good knowledge of ocular and/or parenteral dosage form technologies and laboratory and/or technical tools
  • Good scientific / technical writing skills
  • Good collaboration skills and team spirit enabling you to work in a matrix environment, good communication and negotiation skills
  • Fluent in English (oral and written), German is an advantage

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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