no-953

Compliance & Governance Training Lead (Oncology Medical Affairs) / no-953

Location
CH-Basel
Start
asap
End
07.08.22
Workload
100 %
All-in / Hour
see job description
Total Hours
1900
Deadline
Deadline
31.08.21
no-953

Compliance & Governance Training Lead (Oncology Medical Affairs) / no-953

Location
CH-Basel
Workload
100 %

Start

asap

End

07.08.22

DEADLINE

Deadline
31.08.21

  • CH-Basel
  • Applications have closed
  • no-953CH-Baselasap07.08.22100 % 1900see job descriptionDeadline
    31.08.21

For our customer located in Basel (CH) we are currently looking for a

Compliance & Governance Training Lead (Oncology Medical Affiars) (m/f/x)

 

  • Gross Rate: 68-77 chf gross per hour (given by client)
  • Typical monthly salary with max rate e.g.: 160 h * 77 chf = 12.320 chf gross

Tasks & Responsibilities

  •  Lead design and implementation of “Just-In-Time (JIT)” training concept for OMA
  • Operate and monitor execution of JIT training
  • Advise Pharma Medical Affairs on JIT training implementation
  • Support OMA Global GxP Director on training management and operations (incl assignments and training compliance monitoring)
  • Provide ad-hoc support to key projects (namely GEMS rollout, HCP Experience)

Must Haves

  • Minimum: Scientific qualification (PhD, MSc or Bachelor’s Degree) in an appropriate scientific discipline or quality-related field with an in-depth knowledge of the international pharmaceutical product development process
  • A minimum of 2 years’ experience with GxP requirements, quality management system including risk management and regulatory requirements from main Heath Authorities.
  • Expertise in the principles and practices of Quality Risk management and / or GxP audits
  • Pharma experience
  • FDA Knowledge is an Advantage
  • Should be familiar with Quality management, Risk management, documentations in a compliant way, should be hands-on
  • Strong analytical and planning skills
  • Able to understand and work with enterprise and functional systems & data
  • Experienced in implementing and deploying projects/ changes in an organization
  • A broad understanding of Quality Management, GCP / GVP and Risk Management processes
  • A broad understanding of main Health Authorities standards (e.g. FDA, EMEA) and ICH regulations and guidelines.
  • Proven self-starter with experience in building capabilities based on defined business needs across geography and functions.
  • Fluent in written and spoken English. Strong and confident communicator both internally at all levels and externally with outside and industry bodies.

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.

Tagged as: compliance, fda, GxP, regulatory, Risk Management

  • CH-Basel
  • Applications have closed
  • no-953CH-Baselasap07.08.22100 % 1900see job descriptionDeadline
    31.08.21

For our customer located in Basel (CH) we are currently looking for a

Compliance & Governance Training Lead (Oncology Medical Affiars) (m/f/x)

 

  • Gross Rate: 68-77 chf gross per hour (given by client)
  • Typical monthly salary with max rate e.g.: 160 h * 77 chf = 12.320 chf gross

Tasks & Responsibilities

  •  Lead design and implementation of “Just-In-Time (JIT)” training concept for OMA
  • Operate and monitor execution of JIT training
  • Advise Pharma Medical Affairs on JIT training implementation
  • Support OMA Global GxP Director on training management and operations (incl assignments and training compliance monitoring)
  • Provide ad-hoc support to key projects (namely GEMS rollout, HCP Experience)

Must Haves

  • Minimum: Scientific qualification (PhD, MSc or Bachelor’s Degree) in an appropriate scientific discipline or quality-related field with an in-depth knowledge of the international pharmaceutical product development process
  • A minimum of 2 years’ experience with GxP requirements, quality management system including risk management and regulatory requirements from main Heath Authorities.
  • Expertise in the principles and practices of Quality Risk management and / or GxP audits
  • Pharma experience
  • FDA Knowledge is an Advantage
  • Should be familiar with Quality management, Risk management, documentations in a compliant way, should be hands-on
  • Strong analytical and planning skills
  • Able to understand and work with enterprise and functional systems & data
  • Experienced in implementing and deploying projects/ changes in an organization
  • A broad understanding of Quality Management, GCP / GVP and Risk Management processes
  • A broad understanding of main Health Authorities standards (e.g. FDA, EMEA) and ICH regulations and guidelines.
  • Proven self-starter with experience in building capabilities based on defined business needs across geography and functions.
  • Fluent in written and spoken English. Strong and confident communicator both internally at all levels and externally with outside and industry bodies.

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.

Tagged as: compliance, fda, GxP, regulatory, Risk Management

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