Senior Regulatory CMC Manager

  • Beschäftigungsart Temporär - bis auf weiteres
  • Ort
    BASEL
  • Referenz 127516-372-2
  • Beginn des Einsatzes 1.9.21
  • Sektor Chemie & Life Sciences
  • Publikationsdatum 13.09.2021
  • Bewerben

You have a degree in a field relating to Life Sciences and gathered experiences in Regulatory Affairs?

Senior Regulatory CMC Manager

Ihr Einsatz

-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)

Ihr Profil

-Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent.
-Languages: Fluent English required (oral and written), Good German (oral and written) desirable
-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

Interessiert?

This multifaceted project provides the opportunity to apply and increase your expert knowledge in one of the largest pharmaceutical companies worldwide. To submit your complete CV including diplomas and references just use the button ‘Apply'. We are looking forward receiving your application today!

Über Manpower
Manpower Schweiz weist über 55 Jahre Erfahrung in der Rekrutierung, Evaluierung und Vermittlung von temporären und festen Mitarbeitenden sowie der Erbringung von HR-Lösungen auf. Mit 50 Agenturen in allen Sprachregionen, 20 000 temporären Mitarbeitenden, 1500 Feststellenvermittlungen und über 5000 Kundenunternehmen aller Grössenordnungen und aus allen Wirtschaftszweigen gehört Manpower zu den Branchenführern in der Schweiz.
 
Unsere 3 Versprechen
„Wir lieben, was wir tun. Dank unserer Leidenschaft haben Sie die besten Einsatzchancen.“
„Wir mögen Menschen. Wie Sie. Darum setzen wir auf eine vertrauensvolle Zusammenarbeit.“
„Wir übernehmen Verantwortung. Das verschafft Ihnen Sicherheit und interessante Perspektiven.“
 
 

Ich will den Job!

Ihr/e Manpower-Berater/in
Sabrina Martino

Life Sciences Competence Center
Picassoplatz 4
4052 Basel

T: +41 58 307 2441



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