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Senior Regulatory Affairs Associate (GMP/PAC)
full-timeTaiwan

Summary

Location

Taiwan

Type

full-time

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About this role

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities:

Act as primary RA representative for local Commercial and medical team: adopt a business perspective, explore opportunities and translate this thinking into actionable plans that fit with strategy.

Assess and mitigate impact of changes with local team

Project Execution

  • Responsible for product and GMP registration dossier preparation and submission of assigned projects.
  • Responsible for timely ordering of registration sample, dossier, certificates etc.
  • Contribute to the discussion of registration plan with both local and global team.
  • Track the registration status in TFDA and timely report to the line manager.
  • Address technical questions from TFDA.
  • Communicate with global/ regional teams on issues related to product registration, TFDA lab product testing
  • Review of promotional materials and labeling.
  • Monitor regulation changes and report in timely manner.
  • Ensure regulatory activities comply with internal Code of Conduct and SOPs
  • Regulatory support to cross functions and department
  • Responsible for product and GMP registration dossier preparation and submission of assigned projects.
  • Responsible for timely ordering of registration sample, dossier, certificates etc.
  • Contribute to the discussion of registration plan with both local and global team.
  • Track the registration status in TFDA and timely report to the line manager.
  • Address technical questions from TFDA.
  • Communicate with global/ regional teams on issues related to product registration, TFDA lab product testing
  • Review of promotional materials and labeling.
  • Monitor regulation changes and report in timely manner.
  • Ensure regulatory activities comply with internal Code of Conduct and SOPs
  • Regulatory support to cross functions and department
  • Works effectively within a team environment but may work independently delivering services within their area of competence

  • Works within broad project guidelines as directed by the project lead and/or technical SMEs

  • Takes initiative to prioritize work to achieve specified project outcomes while confirming alignment with project lead and line manager

  • Capitalizes on opportunities to improve one’s own performance and seeks feedback from the project lead and colleagues

  • Applies information provided by the project lead or senior colleagues to complete assigned project activities

  • Produces quality work that meets the expectations of project lead and the client

  • May serve as a Project Lead for small scale projects or a Work Stream Lead on larger projects, and would be responsible for project planning and set-up and routinely interacts with the assigned Project Specialist (PS) or Project Manager (PM) to appropriately control the project (e.g. project set-up, forecasting and financial entries, invoicing, etc.)

  • Functions as the main client contact and ensures accurate project reporting is in place

  • Ensures that the project team delivers to meet the client expectations for quality and timeliness

  • Ensures that appropriate risk identification and issue-escalation procedures are in place

  • Ensures project specific training compliance of the project team

  • Ensures and/or manages project financials including provision of accurate revenue forecasts

  • Ensures that the project team understand and work to the scope of the contract

  • Identifies new opportunities through Change In Scope or add-on business from existing work

  • Ensures timely project close-out activities are completed

Consulting Activities and Relationship Management

  • Follows and implements the organization’s consulting models and methodologies under the guidance of the project lead and/or Technical SME

  • Delivers consulting services within personal area of expertise under the guidance of the project lead and/or Technical SME

  • Completes assigned activities within project scope and objectives with an understanding of issues which may impact project profitability under the direction of the Project Lead and/or Technical SME

  • Identifies project and internal issues to senior colleagues and Project Lead and/or technical SME and provides proposed solutions

  • Interacts professionally at all working levels within a client organization and within Parexel

  • Identifies project and/or client needs to the Project Lead and or Technical SME and collaborates with senior staff to define a proposed solution

  • Interactions result in clients expressing satisfaction with service provided

  • May assist in preparing and/ or delivering a presentation with the support of senior colleagues

  • Identifies and alerts PC management to opportunities for follow-on business or necessary changes in project scope

Business Development

  • Continue to build a network of industry colleagues through relationships formed during project engagements or through other industry experience

  • Communicates potential new business leads to PC management and account managers

  • May participate in project scoping calls and/or proposal preparation with the support of senior colleagues

Parexel-Related Activities

  • Meets established metrics as specified in scorecard on an annual basis

  • Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, training compliance, project deliverable archiving, participation in internal initiatives/projects as requested by management

  • Defines self-development activities in order to keep current within the industry (i.e. maintain membership in a relevant industry and/or scientific/technical association)

Skills:

  • Project management knowledge

  • Client-focused approach to work

  • Results orientation

  • Teamwork and collaboration skills

  • Excellent interpersonal and intercultural communication skills, both written and verbal

  • Critical thinking and problem-solving skills

  • Proficiency in local language and extensive working knowledge of the English language

Knowledge and Experience:

  • Few years of experience in an industry-related environment

Education:

  • Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline

Other facts

Tech stack
Project Management,Client-Focused Approach,Results Orientation,Teamwork,Collaboration Skills,Interpersonal Skills,Intercultural Communication,Critical Thinking,Problem-Solving Skills,Proficiency in Local Language,Working Knowledge of English

About Parexel

Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 24,000+ professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™ We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award.

Community Guidelines

Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.

We reserve the right to remove comments that do not adhere to our guidelines and report users who violate the rules of our page.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing

What you'll do

  • The Senior Regulatory Affairs Associate will act as the primary regulatory affairs representative for local commercial and medical teams, ensuring compliance with regulations and managing product registration processes. They will also track registration status and communicate with global teams regarding product registration issues.

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Frequently Asked Questions

What does a Senior Regulatory Affairs Associate (GMP/PAC) do at Parexel?

As a Senior Regulatory Affairs Associate (GMP/PAC) at Parexel, you will: the Senior Regulatory Affairs Associate will act as the primary regulatory affairs representative for local commercial and medical teams, ensuring compliance with regulations and managing product registration processes. They will also track registration status and communicate with global teams regarding product registration issues..

Why join Parexel as a Senior Regulatory Affairs Associate (GMP/PAC)?

Parexel is a leading Pharmaceutical Manufacturing company.

Is the Senior Regulatory Affairs Associate (GMP/PAC) position at Parexel remote?

The Senior Regulatory Affairs Associate (GMP/PAC) position at Parexel is based in Taiwan. Contact the company through Clera for specific work arrangement details.

How do I apply for the Senior Regulatory Affairs Associate (GMP/PAC) position at Parexel?

You can apply for the Senior Regulatory Affairs Associate (GMP/PAC) position at Parexel directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Parexel on their website.