no-039

Junior Regulatory Affairs Manager / no-039

Location
4056 Basel
Start
asap
End
31.01.2022
Workload
100 %
All-in / Hour
please ask us
Total Hours
1.920 h
Deadline
Deadline
29.01. 12am
no-039

Junior Regulatory Affairs Manager / no-039

Location
4056 Basel
Workload
100 %

Start

asap

End

31.01.2022

DEADLINE

Deadline
29.01. 12am

  • 4056 Basel
  • Applications have closed
  • no-0394056 Baselasap31.01.2022100 % 1.920 hplease ask usDeadline
    29.01. 12am

For our customer located in Basel/Switzerland we are currently looking for a: Junior Regulatory Affairs Manager(m/f/d)

  • Location: CH-4056 Basel
  • Branch: pharma
  • Duration: 1 year +

Tasks & Responsibilities

Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.

  • Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle
  • Prepare CMC responses to health authority questions during development, registration and product lifecycle
  • Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines
  • Identify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible
  • Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends
  • Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned
  • Establish and maintain sound working relationships with partners and customers
  • Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).

Must Haves

  • Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
  • Fluent English  (oral and written)
  • Regulatory experience preferred, and/or experience in drug/biopharmaceuticals
  • Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines
  • Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable
  • Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload
  • Effective planning, organizational and interpersonal skills
  • Reasonable approach to risk assessment
  • Excellent written/spoken communication and negotiation skills
  • Computer literacy

Nice to Haves

  • Good german skills (oral)
  • Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent

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: CMC, documentation, NCEs, regulatory submissions, strategy

  • 4056 Basel
  • Applications have closed
  • no-0394056 Baselasap31.01.2022100 % 1.920 hplease ask usDeadline
    29.01. 12am

For our customer located in Basel/Switzerland we are currently looking for a: Junior Regulatory Affairs Manager(m/f/d)

  • Location: CH-4056 Basel
  • Branch: pharma
  • Duration: 1 year +

Tasks & Responsibilities

Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.

  • Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle
  • Prepare CMC responses to health authority questions during development, registration and product lifecycle
  • Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines
  • Identify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible
  • Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends
  • Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned
  • Establish and maintain sound working relationships with partners and customers
  • Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).

Must Haves

  • Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
  • Fluent English  (oral and written)
  • Regulatory experience preferred, and/or experience in drug/biopharmaceuticals
  • Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines
  • Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable
  • Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload
  • Effective planning, organizational and interpersonal skills
  • Reasonable approach to risk assessment
  • Excellent written/spoken communication and negotiation skills
  • Computer literacy

Nice to Haves

  • Good german skills (oral)
  • Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent

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: CMC, documentation, NCEs, regulatory submissions, strategy

SIGN IN JOB ALERT

Click on the button to load the content from t2b64de1b.emailsys1a.net.

Load content