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Senior Process & Project Engineer II

AbbVie · Singapore · Full-time

8+ years Posted 23 Jan 2026

Quick Summary

  • Assist in design, operation, control and optimization of chemical/biological processes.
  • Lead modifications, troubleshooting, and deviation investigations in cGMP environment.
  • Provide operational support for manufacturing systems of API and biologic products.

Full Description

Company Description:

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description:

 

  • Assist in the design, operation, control and optimization of chemical / biological processes.
  • To be part of 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.
  • Participate in improvement efforts leading to  higher 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.
  • Assist in development of 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.
Qualifications:
  • Bachelor’s Degree in Engineering.
  • At least 8+ years of relevant work experience.
  • 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.
  • Good communication skills.
  • Ability to work well with teams including external contractors.
  • Excellent team player willing to work for the common goal.
Additional Information:

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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