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Regulatory Affairs CMC Associate Manager
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client
Projektbeschreibung
For our client in BASEL we are looking for a REGULATORY AFFAIRS CMC ASSOCIATE MANAGER for a 1-YEAR contract.
DURATION: 1 YEAR
LOCATION: BASEL
WORKLOAD: 100%
ABOUT THE ROLE:
Under supervision the candidate will provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.
THE CANDIDATE'S PROFILE:
- Degree in Science (eg Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
- Preferred: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent
- Fluent English
- Preferred: English, German
- Regulatory experience preferred (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.
TASKS & RESPONSIBILITIES:
1. 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 life cycle.
2. Prepare CMC responses to health authority questions during development, registration and product life cycle.
3. Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
4. 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.
5. Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.
6. Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.
7. Establish and maintain sound working relationships with partners and customers.
8. 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).
For further details please contact Beata Arciszewska:
email: (see below)
DURATION: 1 YEAR
LOCATION: BASEL
WORKLOAD: 100%
ABOUT THE ROLE:
Under supervision the candidate will provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.
THE CANDIDATE'S PROFILE:
- Degree in Science (eg Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
- Preferred: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent
- Fluent English
- Preferred: English, German
- Regulatory experience preferred (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.
TASKS & RESPONSIBILITIES:
1. 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 life cycle.
2. Prepare CMC responses to health authority questions during development, registration and product life cycle.
3. Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
4. 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.
5. Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.
6. Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.
7. Establish and maintain sound working relationships with partners and customers.
8. 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).
For further details please contact Beata Arciszewska:
email: (see below)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges