Senior Expert Science & Technology / no-552

Location
CH-Basel
Start
asap
End
28.02.23
Workload
100 %
All-in / Hour
rate: see jobdescription
Total Hours
1440

Deadline:

Deadline
30.05.22

 

Senior Expert Science & Technology / no-552

Location
CH-Basel
Workload
100 %

Start

asap

End

28.02.23

DEADLINE

Deadline
30.05.22

  • CH-Basel
  • Applications have closed
  • CH-Baselasap28.02.23100 % 1440rate: see jobdescriptionDeadline
    30.05.22

For our customer located in Basel/Switzerland we are currently looking for a: Senior Expert Science & Technology (m/f/x)

 

 

Pay Rate Range (given by client): 55,77 – 62,74 chf/hr gross

Tasks & Responsibilities

Profile Details

  • Design, plan, perform, interpret and report results of scientific experiments for the
    preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD strategies and goals.

 

Management Track

  • Lead a team for the development of pharmaceutical/biological/cell-gene therapies working
    in a multidisciplinary environment. Execute and support developing the functional strategy
    and drive operational excellence in line with TRD vision and strategy. Ensure full
    portfolio support in line with GDD, Sandoz, NTO and NIBR plans.

 

Team Lead:

  • -Lead and manage a team developing generic products, processes and procedures in line with global technical development strategy and objectives; apply scientific/technical/ GMP
    and/or quality-related expertise to address complex R&D issues; coach team members; manage operational aspects in lab; develop strategies on science and technologies.

 

(Principal) Scientist: 

  • Lead and manage all project/local network activities and contribute
    to strategic decisions; design, plan, perform, document and interpret scientific/developmental experiments or GMP testing or pilot plant processes for the preparation and timely delivery of generic products, processes or procedures within a multi functional project team coordinated by a Project Manager/Leader; maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned.

 

Major Accountabilities

  • Oversee and lead all activities of assigned teams /projects; meet customer needs.

  • Work according to appropriate standards for quality, ethics, health, safety, environment,protection and information security; lead initiatives to ensure continuous improvement; allactivities have to be aligned with organizational workflows and procedures.

     

  • Evaluate and interpret results, draw relevant conclusions; supervise project related
    activities; perform complex tasks without having established procedures.

     

  • Oversees and may also write protocols, scientific reports, lab procedures or process. related SOPs; write scientific documents intended for external partners or for generation
    of registration documents; interact with authorities.

     

  • Communicate, address and solve problems within own and broader area of responsibility,
    communicate effectively across organizational interfaces; lead the transfer of know how to
    other departments or external contractors, including troubleshooting and on-site training.

     

  • For technical development units: Develop complex methods (lab or plant); lead the
    optimization of project related scientific /technical activities or processes, co-ordinate
    local team(s); guide development and implementation of new technologies.

     

  • For GMP units: ensure compliance to cGMP.

  • For technology focused role: Provide scientific and technical guidance; actively foster
    knowledge exchange. Develop, mentor and coach other scientific associates; present
    scientific /technical results internally and contribute to publications, presentations and
    patents.

     

  • For project-focused role: Lead assigned teams; represent own technical function in teams
    and fulfil all project tasks and responsibilities related to the own discipline.

     

  • Broadly uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.

     

  • Contributes to many cost center goals and objectives; may contribute to service line goals

  • Responsible for providing scientific leadership and project management for multiple projects.
  • Plan, coordinate, implement and take full responsibility for all designated tasks associated with formulation development.
  • Develop detailed plans and timelines with the manager, develop formulation strategies and plans for designated projects from development to cGMP manufacture.
  • Ensure accurate, speedy reports are produced to enable regulatory filings.

Must Haves

  • Language English written and spoken (highly proficient)

  • German is an advantage

  • We will need candidates with preferably PhD and working experience in analytics in the field of cell biology, as well as experience in cell culture and preferably in bioassays.

     

     

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.

  • CH-Basel
  • Applications have closed
  • CH-Baselasap28.02.23100 % 1440rate: see jobdescriptionDeadline
    30.05.22

For our customer located in Basel/Switzerland we are currently looking for a: Senior Expert Science & Technology (m/f/x)

 

 

Pay Rate Range (given by client): 55,77 – 62,74 chf/hr gross

Tasks & Responsibilities

Profile Details

  • Design, plan, perform, interpret and report results of scientific experiments for the
    preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD strategies and goals.

 

Management Track

  • Lead a team for the development of pharmaceutical/biological/cell-gene therapies working
    in a multidisciplinary environment. Execute and support developing the functional strategy
    and drive operational excellence in line with TRD vision and strategy. Ensure full
    portfolio support in line with GDD, Sandoz, NTO and NIBR plans.

 

Team Lead:

  • -Lead and manage a team developing generic products, processes and procedures in line with global technical development strategy and objectives; apply scientific/technical/ GMP
    and/or quality-related expertise to address complex R&D issues; coach team members; manage operational aspects in lab; develop strategies on science and technologies.

 

(Principal) Scientist: 

  • Lead and manage all project/local network activities and contribute
    to strategic decisions; design, plan, perform, document and interpret scientific/developmental experiments or GMP testing or pilot plant processes for the preparation and timely delivery of generic products, processes or procedures within a multi functional project team coordinated by a Project Manager/Leader; maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned.

 

Major Accountabilities

  • Oversee and lead all activities of assigned teams /projects; meet customer needs.

  • Work according to appropriate standards for quality, ethics, health, safety, environment,protection and information security; lead initiatives to ensure continuous improvement; allactivities have to be aligned with organizational workflows and procedures.

     

  • Evaluate and interpret results, draw relevant conclusions; supervise project related
    activities; perform complex tasks without having established procedures.

     

  • Oversees and may also write protocols, scientific reports, lab procedures or process. related SOPs; write scientific documents intended for external partners or for generation
    of registration documents; interact with authorities.

     

  • Communicate, address and solve problems within own and broader area of responsibility,
    communicate effectively across organizational interfaces; lead the transfer of know how to
    other departments or external contractors, including troubleshooting and on-site training.

     

  • For technical development units: Develop complex methods (lab or plant); lead the
    optimization of project related scientific /technical activities or processes, co-ordinate
    local team(s); guide development and implementation of new technologies.

     

  • For GMP units: ensure compliance to cGMP.

  • For technology focused role: Provide scientific and technical guidance; actively foster
    knowledge exchange. Develop, mentor and coach other scientific associates; present
    scientific /technical results internally and contribute to publications, presentations and
    patents.

     

  • For project-focused role: Lead assigned teams; represent own technical function in teams
    and fulfil all project tasks and responsibilities related to the own discipline.

     

  • Broadly uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.

     

  • Contributes to many cost center goals and objectives; may contribute to service line goals

  • Responsible for providing scientific leadership and project management for multiple projects.
  • Plan, coordinate, implement and take full responsibility for all designated tasks associated with formulation development.
  • Develop detailed plans and timelines with the manager, develop formulation strategies and plans for designated projects from development to cGMP manufacture.
  • Ensure accurate, speedy reports are produced to enable regulatory filings.

Must Haves

  • Language English written and spoken (highly proficient)

  • German is an advantage

  • We will need candidates with preferably PhD and working experience in analytics in the field of cell biology, as well as experience in cell culture and preferably in bioassays.

     

     

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.

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