• Our Client is a well-established Pharmaceuticals MNC.

Responsibilities:

• Manage the regulatory submission process by ensuring timely supply of supporting information and regulatory dossier review to achieve timely approval from regulatory authorities.
• Manage questions from regulatory authorities concerning a regulatory submission by ensuring timely supply of response and supporting information to achieve timely approval from authorities.
• Manage the implementation of registered commitments to ensure continuous compliance with inspection requirements.
• Support site change control, investigations and batch release, improvement initiatives through the provision of regulatory advice and act as an initiator or enabler for change implementation.
• Support external and internal audits.
• Act as the QA for the review and subsequent implementation actions for changes to pharmacopoeia requirements.
• Conduct expert reviews of information, facilities and practices used by the business and external parties to ensure implementation of required regulatory strategies and compliance with standards.

Requirements:

• Bachelor Degree in related discipline.
• At least 3 years of relavent working experience, preferably from Pharmaceuticals industry.
• Able to start work immediately or within short notice.
• Ability to commit for the entire Contract period.

​​Other Information:

• Twelve (12) Months' Contract.
• Working Location: West.
• Working Hours: Mondays to Fridays, 8.30am to 5.30pm.
• Critical: Due to the organization's affirmed support and commitment to developing a Singaporean core, this role is only available to Singaporeans.

To apply, please visit www.gmprecruit.com and search for Job Reference: 20301.
To learn more about this opportunity, please contact Novita Tan at novita.tan@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Recruitment Services (S) Pte Ltd | EA License: 09C3051 | EA Personnel: Novita Tan | Registration No: R1220374