Analytical Expert (80-100%) / no-380

Location
CH-Basel
Start
06.01.2025
End
05.07.2026
Workload
80-100 %
All-in / Hour
see job description
Total Hours
3120

Deadline:

Deadline
30.10.2024

 

Analytical Expert (80-100%) / no-380

Location
CH-Basel
Workload
80-100 %

Start

06.01.2025

End

05.07.2026

DEADLINE

Deadline
30.10.2024

  • CH-Basel
  • CH-Basel06.01.202505.07.202680-100 % 3120see job descriptionDeadline
    30.10.2024

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

  • Duration: 06.01.25 – 05.07.26

  • Workload: 80-100%

  • Location: Basel

  • Payrange, defined by client: 39,55 – 49,08 chf/h, Example: for a month with 160 worked hours*49,08 chf = 7.852,80 chf gross salry

Tasks & Responsibilities

14! This is the number of Radio Ligand Therapy (RLT) projects of our rich and fast-growing development pipeline. We are looking for an Analytical Expert to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Global Drug Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated, experienced Analytical Expert with a strong background and experience in parenteral development to join our team. Expertise in RLT or peptide analytics is an asset.

  • Plan, interpret and report results of scientific experiments for timely supply of drug substances (DS) and drug products (DP).

  • Write & review analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and align the corresponding activities within a global project team.

  • Manage interactions with internal and external stakeholders, including outsourced activities to CROs by providing scientific and technical guidance whenever necessary.

  • Proactively identify scientific, technological and GMP challenges, propose creative solutions and communicate key issues to the Analytical Project Leader or respective technical project team.

  • Work according to appropriate SOPs, GMP, Quality Directives, Health and Safety & internal our clients guidelines.

  • Provide valuable input to the analytical CMC documents and support regulatory submissions.

  • Drive, lead, and manage analytical activities including impurity profiling related to the analytical development of RLTs compounds (e. g. method development, validation, stability, and release testing).

  • Provide scientific guidance to the cross-functional and global project teams and thereby scientifically driving our exciting RLT portfolio.

  • Display a collaborative and inspired attitude within project teams and our stakeholders and partners is key.

Must Haves

  • PhD or minimum Master in analytical chemistry or equivalent

  • At least 2-4 years’ experience in the pharmaceutical industry with a track record in GMP activities for development or marketed products.

  • Profound expertise in analytical raw data documentation, documentation writing (Stability Report, Validation etc)

  • Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences, ability to perform in a highly dynamic environment.

  • Advanced knowledge of laboratory and/or technical tools (e.g. HPLC, LC-MS, Quality management systems, statistical evaluation tools …)

  • Good knowledge of commonly used software and computer tools.

  • Good scientific/technical writing skills.

  • Eager to develop new methods and assess new analytical techniques.

  • Proven leadership in guiding and mentoring colleagues

  • Strong coordination skills, collaborative spirit, self-driven attitude, high level of learning agility.

  • Strong quality focus

  • Excellent communication and role model skills

  • Fluent in English (oral and writing)

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-Basel06.01.202505.07.202680-100 % 3120see job descriptionDeadline
    30.10.2024

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

  • Duration: 06.01.25 – 05.07.26

  • Workload: 80-100%

  • Location: Basel

  • Payrange, defined by client: 39,55 – 49,08 chf/h, Example: for a month with 160 worked hours*49,08 chf = 7.852,80 chf gross salry

Tasks & Responsibilities

14! This is the number of Radio Ligand Therapy (RLT) projects of our rich and fast-growing development pipeline. We are looking for an Analytical Expert to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Global Drug Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated, experienced Analytical Expert with a strong background and experience in parenteral development to join our team. Expertise in RLT or peptide analytics is an asset.

  • Plan, interpret and report results of scientific experiments for timely supply of drug substances (DS) and drug products (DP).

  • Write & review analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and align the corresponding activities within a global project team.

  • Manage interactions with internal and external stakeholders, including outsourced activities to CROs by providing scientific and technical guidance whenever necessary.

  • Proactively identify scientific, technological and GMP challenges, propose creative solutions and communicate key issues to the Analytical Project Leader or respective technical project team.

  • Work according to appropriate SOPs, GMP, Quality Directives, Health and Safety & internal our clients guidelines.

  • Provide valuable input to the analytical CMC documents and support regulatory submissions.

  • Drive, lead, and manage analytical activities including impurity profiling related to the analytical development of RLTs compounds (e. g. method development, validation, stability, and release testing).

  • Provide scientific guidance to the cross-functional and global project teams and thereby scientifically driving our exciting RLT portfolio.

  • Display a collaborative and inspired attitude within project teams and our stakeholders and partners is key.

Must Haves

  • PhD or minimum Master in analytical chemistry or equivalent

  • At least 2-4 years’ experience in the pharmaceutical industry with a track record in GMP activities for development or marketed products.

  • Profound expertise in analytical raw data documentation, documentation writing (Stability Report, Validation etc)

  • Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences, ability to perform in a highly dynamic environment.

  • Advanced knowledge of laboratory and/or technical tools (e.g. HPLC, LC-MS, Quality management systems, statistical evaluation tools …)

  • Good knowledge of commonly used software and computer tools.

  • Good scientific/technical writing skills.

  • Eager to develop new methods and assess new analytical techniques.

  • Proven leadership in guiding and mentoring colleagues

  • Strong coordination skills, collaborative spirit, self-driven attitude, high level of learning agility.

  • Strong quality focus

  • Excellent communication and role model skills

  • Fluent in English (oral and writing)

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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