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PharmEng Technology supports multiple small to multinational company MNC clients in the field of Regulatory Affairs Consulting, Pharmacovigilance, GMP Validation & Qualification Engineers, QA QC, Manufacturing Technicians, etc. There will be various job openings via outsourcing with our Clients thoughout the year, in Singapore, Malaysia and even other countries. Feel free to drop your CV with us at for various consulting opportunities, where you can gain work experience for recognition in the pharmaceutical industry. We will contact you with the detailed job description when the right fit comes along!  

Current Job Openings - Click on links to see full Job Description
Regulatory Affairs Positions

Various tasks. On-site local and / or regional positions, junior to senior level Regulatory Consulting opportunities. Upkeep the Chemistry Manufacturing and Controls (CMC) part of dossier, gap analysis, product submissions, maintain product life cycle variations, project management etc., for multi product category submissions for NDA, NCE, Generics, Biologics, BIosimilars, Medical Devices, Cosmetics, Health Supplements etc

Others: Quality Assurance, SOP writing, management of Quality Management Systems, Good Manufacturing, Good Distribution Practice Consulting etc. 

Support Pharmaceutical and Biologic Manufacturing plants in various Technical positions, Engineering Facility design and support roles, maintenance roles in building, environment, production, oversee the asset care and maintenance of all mechanical equipment, comply to company EHS guidelines with cGMP, HSE, Statutory, Regulatory/Authority requirements in executing maintenance, troubleshooting and repair activities following procedures and instructions. Produce high-quality documentation in line with guidelines, to work collaboratively with different stakeholders from cross functional teams/ experts to deliver Manufacturing process documentation on time etc.

Role summary

If you are passionate about Quality, Safety and Efficacy of pharmaceutical, biological products and medical devices, and would love to be part of our team to ensure regulatory compliance of these products for the benefit of the patient or consumer, email your CV to and we will be in touch with you for further discussion.


Requirement summary

At least 2 years experience in Regulatory Affairs, Engineering and/or Quality Assurance in the Pharmaceuticals and Biotechnology space, with at least Bachelors of Science, Pharmacy or Egineering in relevant field.

Note that only shortlisted candidates will be notified.



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