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Take lead in regulatory activities for the business to ensure company products are align with local regulations. Making sure all data are correct such as labeling, packaging, artwork etc.
Be part of one of the top global pharmaceutical companies in the industry. Take lead in RA Development strategy to obtain/maintain unmet medical needs.
Be part of one of the leading global bio-pharma companies in the industry. Take lead in post-RA activities for the company as well as lead a small team.
Be part of a top global pharmaceutical company in the industry. Take lead in CMC RA and QA activities as well as serving as the Hinseki.
Be part of one of the top life science business in the world. Take lead in RA activities to obtain/maintain business licenses and products.
Be part of one of the top global diagnostics companies in the industry. Take lead in product submissions/maintenance for IVD and MD areas.
Be part of one of the top global medical device companies in the industry. Lead in RA product applications for class I-IV products to obtain approval.
Be part of one of the leading biopharmaceutical companies in the industry. Take lead in RA development strategies as well as lead the RA team.
Take lead in RA activities to obtain product approval. Ensure effective submission requirements as well proper timelines of new/existing regulatory projects.
Lead in RA activities to obtain regulatory approval for company products. Expand the business into the Japanese market.
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