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Specialist, International Labeling Support

atMSD (Thailand) Co., Ltd.

Job Description Specialist, International Labeling Support The Opportunity Exciting opportunity to join an innovative and trusted Global biopharmaceutical company Permanent Full-time opportunity Work autonomously whilst being supported, encouraged and being part of a trusted Global leading Pharmaceutical organization The Specialist, International Labeling Support (ILS) will partner cross functionally within Global Regulatory Affairs & Clinical Safety (GRACS) and cross divisionally where applicable to ensure Labeling and Artworks regulatory operational activities within scope of ILS are planned, managed, and executed timely, accurately and in a compliant way. The role is responsible for supporting local labeling implementation activities, maintaining regulatory records and databases, and driving operational excellence through continuous process improvement initiatives. What you will do: Prepares high-quality labeling and artwork package aligned in accordance with company requirements and provides operational support to Country Regulatory Affairs (CRA) for regulatory activities (database maintenance, regulatory record management) within the ILS scope of work. Ensure labeling and artwork deliverables are completed accurately and within established timelines. Supports the preparation of the metrics for the designated business process. Collaborates with Global Labeling, CRA, and other stakeholders to resolve labeling and artwork-related queries. Supports necessary updates to process documentation, work instructions, and training materials. Participate in cross-functional initiatives that identify opportunities to improve, simplify, and streamline processes and tools. What You Must have Bachelor's degree (Pharmaceutical Sciences, Biotechnology, Life Sciences, Pharmacy, or a related discipline is preferred) Minimum 2 years of experience in the pharmaceutical, biotechnology, healthcare, or related industry. Prior experience in Regulatory Affairs, labeling and artwork management, CMC, quality, compliance, or regulatory operations is preferred. Experience with regulatory systems, databases, or document management systems is an advantage. Strong organizational skills with the ability to manage multiple priorities and meet deadlines. Good interpersonal and communication skills, with the ability to collaborate effectively across functions and regions. Detail-oriented with a strong focus on quality, accuracy, and compliance. Proficient in Microsoft 365 applications Open to exploring emerging technologies, including AI-enabled solutions, and applying them creatively and responsibly to enhance business processes and ways of working. Required Skills: Biological Sciences, Biotechnology, Business Processes, Continuous Process Improvement, Detail-Oriented, Emerging Technologies, Life Science, Operational Excellence, Pharmaceutical Regulatory Affairs, Pharmaceutical Sciences, Process Documentation, Regulatory Affairs Compliance Preferred Skills: Communication, Creativity, Customer Engagement, Empathy, FDA Regulations, Global Force Management, Incentive Compensation, Medical Affairs, Organizational Behavior, Regulatory Compliance, Sales Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 08/28/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Experience required
  • 2 years
Salary
  • Negotiable
Job function
  • Quality Assurance
  • Legal
Job type
  • Full-time

Company overview

Size:2000-5000 employees
Industry:Advertising / Media
Location:Bangkok
Website:www.merck.com
Founded in:2004
Ranking:4/5

Merck & Co., Inc. (Merck) is a global research-driven pharmaceutical company that discovers, develops, manufactures and markets a range of products to improve human and animal health. The Company?s operations are principally managed on a products basis and comprises of two business segments: the Pha ... Read more

Why join us: Joining MSD Thailand means becoming part of a team that values diversity, inclusion, and a shared commitment to making a difference. We offer a career experience like no other, empowering you both professionally and personally. Our 'Total Rewards' philosophy includes competitive compensation, compre ... Read more

Head office: 999/9 DI OFFICE SET AND CENTRAL WORLD BUILDING CHAN 37 HONG M H 3701-3712 THANON RAMA I
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