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Regulatory Affairs Specialist

CHİL TIBBİ MALZEME SAN.VE TİC.LTD.ŞTİ.

İzmir(Çiğli)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Position Level

Specialist

Department

Quality

Quality

Application Count

155 application

Job Type

Full-Time

Position Level

Specialist

Application Count

155 application

Department

Quality

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QUALIFICATIONS AND JOB DESCRIPTION

We are looking for dynamic, friendly, hard working, enthusiastic, resilient, talented and most importantly an idealistic candidates for 'Regulatory Affairs Specialist' role.

Qualifications

  • Bachelor degree in Engineering or Science or Health/Life Sciences departments of universities. MSc, PhD is an assets.
  • Preferably 2 to 3 years experience in Regulatory Affairs Management in a multinational environment (medical industry would be an asset).
  • Working knowledge of regulatory registrations in local and international.
  • Working knowledge with ISO 13485, MDD (93/42/EC), IVDD (98/79 EC), FDA requirements and the other global regulations.
  • Good knowledge in MS Office software (Word, Excel, Powerpoint, Outlook) is required.
  • Excellent command of written & spoken English is compulsory.
  • Team player with excellent communication and presentation skills; able to develop collaborative relationships with various stakeholders and authorities both internal and external to achieve objectives.
  • Analytical thinking, result and solution oriented, innovative, proactive, flexible and strong ability on problem solving and reporting. Must be able to identify creative options for resolving issues that respond to multiple stakeholder and authorities interests and needs,
  • Strong and prompt planning, follow up, reporting, coordination and organization skills to achieve accurate and timely results.
  • Be confident, positive, self-motivated& able to work independently
  • Good communication skills
  • Teamwork oriented, ability to establish and maintain effective working relationships
  • Willing to learn, research and improvement


Job Description

  • Implement and support registration and re-registration tasks with the authorities.
  • Support the establishment and development of the RA sytem.
  • Responsible for coordination and implementation of RA activities in line with international regulations, Chil Ltd. policies and procedures.
  • Ensure the completion of regulatory certification/registration/notification/listing activities in a correct and timely manner.
  • Evaluate the effects of change control activities from regulatory perspective and implement required regulatory steps on a timely manner.
  • Follow the currency and delivery of quality documents and records to the third parties during registration activities.
  • Follow-up of developments and changes in the local & international regulatory policy rules, legislations and guidelines with impact to Chil Ltd. activities. Analyze available regulatory and compliance information.

    

  We look forward to receiving your application. 

Preferred Candidate

No experience preference
Bachelor’s(Graduate), Master’s(Graduate), Doctorate(Graduate)
Completed
English(Reading : Advanced, Writing : Advanced, Speaking : Advanced)
Class B

Regülasyon Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Regülasyon Uzmanı Regülasyon Uzmanı Maaşları Regülasyon Uzmanı Nasıl Olunur? Regülasyon Uzmanı Nedir? Regülasyon Uzmanı İş İlanları
Şirketin Aydınlatma Metni

1CHİL TIBBİ MALZEME SAN. VE TİC. LTD. ŞTİ. ÇALIŞANLARINA İLİŞKİN KİŞİSEL VERİLERİN KORUNMASI HAKKIND

Detaylı Bilgi

Regülasyon Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Regülasyon Uzmanı Regülasyon Uzmanı Maaşları Regülasyon Uzmanı Nasıl Olunur? Regülasyon Uzmanı Nedir? Regülasyon Uzmanı İş İlanları