ABOUT US We have begun a journey towards growth, as part of a shift in adapting to the new generation of workforce. We are dedicated to our build teams differently to focus on servant leadership in our management. We believe every talent can bring and find their life purpose through the efforts that we all invest into our work. We apply leadership principles in our everyday discussions to deliver the best results from creating new value through projects and empowering our team to make great decisions. We are the leaders in innovation of our industry and we want you to be part of our innovation environment where you will find yourself being great innovators who bring value to the world and always pursuing to be a better version of yourself. THE ROLE & REQUIREMENTS The role will be responsible for the oversight and execution of quality related activities through all stages of clinical development to global commercialisation. Responsibilities will include leading the development and implementation of policies, procedures and protocols to control GMP activities, implementation of GMP standards and on-going compliance initiatives and regulations. The role will obviously involve interaction with global colleagues, internal stakeholders and external suppliers. Other key responsibilities will include but not be limited to:

• Serve as GMP Quality Management for assigned programs.

\xc2\xb7 Develop and follow procedures for the oversight of quality aspects of pharmaceutical development in an outsourcing environment, including the quality aspects of process and formulation development, manufacturing, analytical testing, packaging, product release and associated stability programs.

• Perform quality activities such as: validation protocols, report, review and approval, specification review and approval, batch record review, approval and release to ensure timely delivery of finished products to support the clinical development plan as well as commercial sales plan.
• Oversee supplier quality management activities for assigned suppliers. Oversight will include confirmation of compliance, management/conduct of quality audits and inspection readiness activities and appropriate resolution of CAPA plans as required.
• Perform and participate in internal audits as assigned.

Successful applicants must be able to demonstrate excellent quality experience as well as 5+ years of hands on QA/QMS experience ideally within a cosmetics manufacturing or any relevant environment. You must also be able to show: \xc2\xb7 A demonstrated ability to develop and implement procedures which ensure compliance to GMP and regulatory standards. \xc2\xb7 Demonstrated audit conduct and management experience. \xc2\xb7 Demonstrated knowledge, understanding and application of GMP guidelines and regulations. \xc2\xb7 Fluent English communications skills (written & spoken).
Considerable knowledge of cosmetic development process, ISO 13485,HALAL, ISO22716, NPRA guidelines and GMPs. Job Type: Full-time Salary: RM2,500.00 - RM3,500.00 per month Benefits:

• Maternity leave
• Opportunities for promotion
• Parental leave
• Professional development

Schedule:

• Day shift
• Monday to Friday

Education:

• Bachelor\'s (Preferred)

Experience:

• Pharmaceutical QMS Executive: 3 years (Required)

Expected Start Date: 04/15/2024