Lead Process Project Engineer
Lead Process Project Engineer
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Job Description
- 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 buildouts.
- 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.
Qualifications :
- Bachelors degree or a diploma in Engineering.
- At least 9 years of relevant work experience.
- Knowledge of cGMP is highly preferred.
- Strong technical knowledge coupled with handson working experience in a pharmaceutical / biotech facility.
- Working experience in startups 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.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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No
Employment Type :
Fulltime
Employment Type
Full-time
