Regulatory Specialist

Gravitiq; Singapore; Remote; SGD 75,000 - 100,000; Full time

Job summary

Gravitiq is seeking a Compliance Specialist with expertise in regulatory affairs, particularly in the medical device sector. The role involves ensuring compliance with international standards, conducting audits, and maintaining documentation. This full-time position offers a permanent remote setup, performance-based bonuses, and a collaborative and youthful work environment.

Benefits

Performance-based bonus

Paid annual leaves & UK banking holidays

Annual salary reviews

Supportive and fun environment

Qualifications

• At least 5 years of experience in the regulatory arena, ideally with medical devices.
• Strong background in compliance documentation and audits.
• Exceptional organizational skills and ability to manage multiple tasks.

Responsibilities

• Partner with compliance team to assess compliance risks and document management.
• Steer product launches ensuring compliance with legal requirements.
• Conduct audits of supplier documentation for material compliance.

Skills

Regulatory Compliance

Problem-Solving

Time Management

Organizational Skills

Education

Bachelor's degree in Pharmacy, Life Sciences, or Regulatory Affairs

Tools

MS Office

Slack

Monday.com

Job description

Who We Are:Gravitiq is an e-commerce company based in the United Kingdom. We're at the forefront of the health and wellness revolution and beyond, strategically leveraging digital transformation across diverse consumer sectors like supplements, beauty, and health products. As the world increasingly embraces online channels, we empower businesses with cutting-edge technology and data-driven strategies to achieve scalable and efficient growth.What youll be doing: Partner with our compliance team to proactively identify and assess compliance risks, particularly within the medical device industry, keeping us ahead of the curve. Steer new product launches and market expansions smoothly, ensuring meticulous compliance with legal requirements and managing all essential documentation. Review product categories against international standards, providing expert advice on necessary adjustments to product materials and online listings. Conduct thorough audits of supplier documentation and certifications, ensuring material compliance and fostering strong supplier relationships. Conduct in-depth research on international regulations, providing critical insights to support our global compliance strategy. Uphold and enhance our Quality Management System (QMS), ensuring adherence to regulatory standards and maintaining impeccable documentation. Manage communication with regulatory bodies and authorities, ensuring clear and effective information flow. Organize compliance-related meetings, manage regulatory summaries, and provide vital administrative support to the team.What youll bring into the table: At least 5 years of experience in the regulatory arena, ideally with a focus on medical devices. A Bachelor's degree from a reputable university, preferably in Pharmacy, Life Sciences, or Regulatory Affairs. Proficiency in the MS Office suite and top-tier time management skills. Bonus points for experience with Slack, Monday.com Exceptional organizational skills, the ability to juggle multiple tasks like a pro, and stellar problem-solving and decision-making abilitiesWhy You'll Love Working Here:We're not just about the work; we're about creating a supportive and fun environment where you can thrive. Here's a glimpse of what you can expect and what you should be amenable to: Permanent remote set-up. Independent contractor agreement Long-term and full-time engagement Usage of a time tracker during probation Working only during weekdays, 10AM-7PM UK time zone Performance-based bonus Paid annual leaves & UK banking holidays Annual salary reviews Fun and a youthful environment!If you think you suit the role and youre happy with the above-mentioned terms, please feel free to submit your updated CV and our recruitment team will contact you should you get shortlisted!Job Type: Full-timeBenefits: Work from homeSchedule: Monday to Friday Performance bonusApplication Question(s): Do you have experience on SUPPLEMENTS category Experience: Regulatory: 3 years (Preferred)Work Location: Remote,

• Job Tags qms, quality management, quality assurance

Sign-in & see how your skills match this job

Sign-in & Get noticed by top recruiters and get hired fast