Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Regulatory Affair Specialist

Job

PROCESS ENGINEERING SPECIALISTS PTE. LTD.

Hauppauge, NY (In Person)

$72,000 Salary, Full-Time

Posted 6 days ago (Updated 1 day ago) • Actively hiring

Expires 8/6/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
71
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

PROCESS ENGINEERING SPECIALISTS PTE. LTD. TYPICALLY REPLIES IN 30
DAYSRegulatory Affair Specialist
MCF-2026-1130146
Islandwide Full Time Senior Executive 3 years exp Engineering $5,000to$7,000 Monthly 19 applicationsPosted 02 Jul 2026Closing on 01 Aug 2026 Roles & Responsibilities PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients. This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date. We are currently looking for a Regulatory Affairs Specialist to join us on a permanent role to help us deliver various projects in the Life Sciences Industry. Key Responsibilities Manage product registrations, renewals, variations, and lifecycle activities across Singapore, Thailand, Malaysia, and Taiwan. Support Quality Management System (QMS) maintenance, including SOPs, document control, change control, and CAPA. Ensure compliance with local medical device regulations, ISO 13485, and regional regulatory requirements. Support internal audits, audit readiness, supplier quality, and quality system improvements. Review product labeling, IFUs, complaint handling, post-market surveillance (PMS), and vigilance activities. Collaborate with regional cross-functional teams to support regulatory submissions, quality initiatives, and business objectives. We are currently looking for candidates in Singapore If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Sruthi Srikanth (careers@pes-international.com). If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on
LinkedIn:
 https://www.linkedin.com/company/processengineeringspecialists/mycompany/