トレンド企業

Baxter International
Baxter International

(Sr) RA Specialist

職種オペレーション
経験シニア級
勤務地Taipei, Taiwan
勤務オンサイト
雇用正社員
掲載2ヶ月前
応募する

必須スキル

Project Management

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Summary:

This role is part of organization Taiwan regulatory affairs, involves drugs registration responsibility in Taiwan.Under limited supervision responsible for role-based activities (e.g.: the delivery of regulatory documents/deliverables/packages in support of Baxter’s products/projects. Development/maintenance of Regulatory systems, trackers and databases. Evaluation and dissemination of new/changing regulations, guidance and standards.)

Essential Duties and Responsibilities:

  • Regulatory Strategy: Coordinate with GRA and BU to implement regulatory strategies for product development and commercialization.
  • Document Preparation: Prepare and submit all necessary regulatory documents, such as New Drug Applications (NDA), Plant Master File (PMF), Drug Master File (DMF), Post-marketing activities (License Renewal, Variations) and other submissions to regulatory authorities.
  • Compliance: Ensure ongoing compliance with global regulatory standards, including those set by the Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Taiwan FDA.
  • Agency Liaison: Act as a primary point of contact with regulatory agencies, responding to their inquiries and providing requested information.
  • Cross-Functional Collaboration: Work closely with R&D, QA, PV, manufacturing, BU and marketing teams to ensure regulatory considerations are integrated into all stages of product development.
  • Product Labeling and Advertising: Assess and approve product labeling, packaging, and advertising materials to ensure compliance with regulations and accurate scientific claims.

Qualifications:

  • Expert knowledge of drug regulations• Good communication and problem-solving skills
  • Excellent time management and project management skills
  • Ability to collaborate with cross-functions
  • Pharmacists are preferred.

Education and/or Experience:

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice:

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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Baxter Internationalについて

Baxter International

Baxter International Inc. is an American multinational healthcare company with headquarters in Deerfield, Illinois.

10,001+

従業員数

Deerfield

本社所在地

$11.2B

企業価値

レビュー

10件のレビュー

3.5

10件のレビュー

ワークライフバランス

3.2

報酬

2.8

企業文化

4.1

キャリア

2.9

経営陣

2.7

65%

知人への推奨率

良い点

Supportive team and colleagues

Good benefits and health coverage

Flexible hours and work-life balance

改善点

Heavy workload and high pressure

Poor management and lack of direction

Low compensation and entry-level pay

給与レンジ

0件のデータ

Junior/L3

Intern

Senior

Manager

Junior/L3 · Software Engineer 2

0件のレポート

$121,000

年収総額

基本給

-

ストック

-

ボーナス

-

$102,850

$139,150