Hlavní stranaZaměstnáníNabídky

Zaměstnání - Nabídky

 

Regulatory Affairs Associate

Typ práce: hlavní pracovní poměr

For my client, prestigious biotechnological company I am looking for Regulatory Affairs Associate.

Job Requirement & Education:

The ideal candidate would have the following academic and personal attributes:

  • Education to at least Bachelor’s level in a scientific discipline
  • Prior experience in a GXP regulated environment
  • Good knowledge of the Common Technical Document (CTD) format
  • Good project management skills with the ability to manage several projects and competing priorities
  • Excellent grammatical, editorial and proofreading skills
  • Very good English

In this role, you will provide regulatory support for product development projects, including product development documents and regulatory agency submissions, implementing/managing project regulatory activities, and supporting project teams. More specifically, you will:

  • Define content of regulatory submission dossiers and initiate review and approval of change control as required. Develop and Agree regulatory deliverables and conduct project delivery activities both with internal and external stakeholders to ensure all timelines are met.
  • Ensure quality authoring of core-administrative parts of submissions.
  • Contribute to or prepare administrative and technical components of regulatory agency submissions primarily for the global conduct of clinical trials (EU, US, China and other regions as required) and if applicable in the future for product registration, for post-approval maintenance, in common technical document (CTD) format.
    Contribute to the preparation of regulatory agency meetings and provide all administrative support for these agency interactions.
  • Manage and/or operationalize the delivery of day-to-day regulatory activities for assigned project according to agreed timelines and strategies.
  • Participate as regulatory support on multidisciplinary project teams, which may include nonclinical, clinical science, clinical operations, CMC and other technical subject matter experts, to develop products throughout their life cycle.
  • Ensure compliance with ICH/regional/country-specific regulatory requirement and the company’s policies and processes.
  • Prepare training materials for internal stakeholders and share best practices in the regulatory area.
  • Participate as regulatory support in internal or external project audits and on internal cross-functional initiatives.
  • Conduct as required research of existing product data and published literature relative to global or regional regulatory requirements for the preparation of gap analyses or product development plans.

 

Offer:

  • Interesting work
  • Very good salary
  • Company benefits (e.g. bonus, pension contribution, 1 week extra holiday, sick days, multisport, meal vouchers etc.)
  • Professional growth, good team

Start date is upon agreement.

 

In sending your CV you give your consent to processing and holding of your personal data in accordance to Act. No. 101/2000 Coll. regarding personal data protection by LD Human Resources s.r.o., ID: 24275336 until a written form revocation. Your personal data can be provided to third persons in order to obtain employment, namely after prior approval.

 

Kontaktní osoba:
Ing. Lada Drobišová, MBA

E-mail:
lada.drobisova@LDHR.cz

Telefon:
+420 722 950 10

Vloženo: 7.6.2018

 

OPPI, MPO, EU
Czech Bio

Doporučujeme

Biosimilars

CEBIO a I. etapa JVTP

  • CEBIO
  • BC AV CR
  • Budvar
  • CAVD
  • CZBA
  • Eco Tend
  • Envisan Gem
  • Gentrend
  • JAIP
  • Jihočeská univerzita
  • Madeta
  • Forestina
  • ALIDEA

Provozovatel

Jihočeská agentura pro podporu inovačního podnikání o.p.s.

Články na přání


[načítám anketu]

LinkedIn