Packaging & Labeling Artwork Implementation Manager (Indonesia)

Posted 7 Days Ago
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DKI Jakarta
Hybrid
Mid level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Manage product labeling and artwork for regulatory compliance, lead projects, ensure communication with stakeholders, and advocate for labeling initiatives.
Summary Generated by Built In
Use Your Power for Purpose
We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines .
What You Will Achieve
You will lead the development and maintenance of product labeling and artwork for regulatory compliance and commercialization. You will serve as a regulatory liaison between markets, manufacturing plants, and project teams, providing strategic direction and ensuring compliance with regulations.
  • Provide guidance, lead/co-lead projects, and manage time to meet objectives .

  • Support the development of tools and processes for global label development and approval.

  • Plan, prioritize, and deliver labeling documents according to targets and requirements.

  • Communicate and present information effectively to stakeholders.

  • Develop local labeling documents with strategic and medical input.

  • Review and implement labeling updates, recording key decisions.

  • Serve as an SME for relevant tools and technologies in label development.

  • Ensure compliance with internal SOPs and regulatory requirements.

  • Contribute to continuous improvement of business practices.

  • Advocate for new labeling initiatives to stakeholders.

Here Is What You Need (Minimum Requirements)
  • BA/BS with 4 or more years of experience, or MBA/MS with 2 or more years of experience, or PhD/JD with 0 or more years of experience

  • Strong understanding of regulatory submission processes and requirements.

  • Demonstrated attention to detail and problem-solving skills.

  • Knowledge of external labeling guidelines and regulations and internal labeling policies and procedures.

  • Understand regulatory implications of product strategy with regards to the product label, assessment, and practical management of associated impacts.

  • Excellent written and verbal communication skills essential.

  • Proven project management skills with the ability to lead complex projects.

Bonus Points If You Have (Preferred Requirements)
  • Experience in the pharmaceutical industry.

  • Exceptional organizational skills and attention to detail.

  • Effective problem-solving and negotiation skills.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs

Top Skills

Labeling Tools And Technologies
Regulatory Compliance Tools

What the Team is Saying

Daniel
Anna
Esteban
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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Pfizer Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Typical time on-site: Not Specified
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