Formulation Production Manager

and continuous improvement

* Understand operation process, perform self-evaluation and drive CI

* Work directly 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) 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 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. Formulation knowledge on process, quality and regulatory

* Team leadership and group process skills

* Fluent English in reading, writing & speaking