北京招聘

工作职责:

1. Work closely with local RA, GRA, commercial teams and manufacture sites to manage product label, package through ARTWORK according to the regulation and company requirements.

2. Collaborate with commercial marketing, legal, compliance colleagues to manage Veeva PromoMats, the company digital assets platform. Maintain and revise local SOPs, train and support local end users, review and approve promotional materials from RA point of view.

3. Support RA to communicate with Global colleagues and import agency to import samples and reagents. Update importation relevant regulations and mange import workflow to ensure that samples could be imported timely.

4. Conduct PV responsibilities as PV backup to support PV DPOC manage local PV QMS by following local regulations and company policies.

5. Other tasks assigned by management.

任职资格:

Education:

Master degree,

Major in veterinary pharmacological or Biological

Experience:

- 1-3 years of regulatory affairs experience in pharma or bio products, or R&D, QA , technical support on veterinary production.

Skills, abilities and other requirements:

- Proficient in English

- Knowing to learning

- Drive results

- Good communication skills

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