Total 1 project director job vacancies in d22 jurong jurong island tuas

Purpose Statement

• Responsible for design, operation and optimization of chemical / biologic processes.
• Coordinate and deliver projects actively leading the integration of technical activities with operations including providing technical support to ongoing operations.
• Analyze new processes and evaluate them to assess needs and feasibility of introduction of these processes into the existing facility.

Responsibilities

• Responsible for design, operation, control and optimization of chemical / biological processes.
• To drive the commissioning and qualification effort of the process equipment and associated systems.
• Design, install and commission new production units, monitoring modifications and upgrades and troubleshooting existing processes.
• Improve process capability and production volume while maintaining and improving quality standards.
• In a cGMP environment, lead modifications and changes to processes and equipment, troubleshooting, deviation investigation, identification and completion of corrective and preventative actions.
• Propose and evaluate modifications to equipment, processes and operations to improve safety, increase efficiency and enhance company goals.
• Maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, costs and changeovers.
• To actively seek avenues to improve operational efficiency accruing benefits to the Abbvie businesses in Singapore.
• Actively engaged in developing specifications for process equipment and assist in FAT / SAT of related equipment as part of the new build-outs.
• Participate and lead, when required, in all investigations (contaminations, deviations, and discrepancies) relating to the manufacturing process.
• Develop and implement systems that ensure the process works at the optimum level, to the right rate and quality of output, in order to meet supply needs
• Provide operational support for the successful and uninterrupted operation of manufacturing systems used in manufacture of API and biologic products.
• Act as one of the key contact points and local SME for investigations into utility excursions and deviations and provides resources to ensure fixes.
• Supervise engineers and provide day to day guidance on technical issues.
• To mentor and coach reports.
• Identify equipment and assess plant production capacity.
• Identify means to resolve equipment bottlenecks & optimize production capacity.

Basic Qualifications:

• Bachelor’s degree or a diploma in Engineering.
• At least 9 years of relevant work experience.

Preferred Qualifications:

• Knowledge of cGMP is highly preferred.
• Strong technical knowledge coupled with hands-on working experience in a pharmaceutical / biotech facility.
• Working experience in start-ups, commissioning & qualification of process systems in an operating plant is a plus.
• Excellent leadership and communication skills.
• Ability to lead teams including external contractors.
• Excellent team player willing to work for the common goal.
• Mentoring and coaching skills.