Responsibilities

Manage all PET activity including coordination of support staff, scheduling and continuous improvement

• Understand operation process, perform self-evaluation and drive CI
• Work direcly with PET core team members to remove systemic obstacles that block our ability to achieve sustainable success
• Advise and influence the development and/or adoption of lean tools
• Producing resource planning and scheduling on a daily basis

Manage and control documentation and reports

• Maintaining documentation that compliance to cGMPs, i.e.SOP, internal audit change control, training programme, deviation report and CAPA
• Maintaining compliance to other regulatory
• Maintaining compliance to SOX

Typical People Management responsibility

• Responsible for the process operation (here refer to OSD Packaging) within the PET, to defined process and operational standards.
• Process Facilitators manage teams directly, or via Team Leaders. They are capable leaders and coaches. They manage performance & development of both the team and individuals.
• Delivering hands-on coaching of multiple packing teams by daily meetings, planning, self-organizations, collaborations etc.
• Facilitating frequent status meeting where the team member report to each other, commit to work and identify barriers
• Expanding the understanding and practice of lean process and principles through the organization
• Develop production team and operators capability through coaching, training program and task assignment etc
• Communicate company policies & decisions within process group and ensure they are well understood and followed by staff

Responsibility for GMP/Compliance/SHE

Requirements

• Bachelor degree or above, major in Pharmaceutical engineering or chemical engineering.
• 5 Years of working experience in related sector, 3 years above leadership role in MNC working experience
• Pharma.Packing knowledge on process, quality and regulatory
• Team leadership and group process skills
• Fluent English in reading, writing & speaking