Senior Manufacturing Engineer

Allergan; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company in Singapore seeks a manufacturing specialist to support API production and ensure quality compliance. The ideal candidate will have a Bachelor’s in Engineering, 5+ years of experience in pharmaceutical manufacturing, and the ability to work 12-hour shifts. Responsibilities include continuous improvement initiatives, liaising with engineering, and ensuring compliance with EHS and cGMP standards. This role demands a high level of integrity and problem-solving skills, alongside proficiency in Delta V and MES.

Qualifications

• Bachelor Degree in Engineering (Chemical/Pharmaceutical Engineering) or equivalent technical Degree.
• Minimum of 5 years of pharmaceutical manufacturing experience.
• Able to work comfortably in 12-hour rotating shift (Day/Night).
• Ability to quickly know products and processes to assess performance issues.
• Demonstrates the highest levels of integrity and a strong work ethic.
• Proficiency in Delta V and MES.
• Good knowledge of GxP requirements and regulations.
• Good level of decision making and problem solving.
• Good planning and scheduling skills.
• Good communication skills both verbal and written.
• Good interpersonal skills.

Responsibilities

• Accountable for continuous improvement activities for the manufacturing department.
• Develop and enhance capacity model, implementing programs to improve production efficiency.
• Liaise with Tech Ops and Engineering for new product processes.
• Facilitate troubleshooting activities for timely closure of investigations.
• Communicate company policies and objectives effectively.
• Ensure compliance with EHS performance and legal obligations.
• Review and update manufacturing documentation for cGMP compliance.
• Identify areas for training and operational streamlining.
• Oversee troubleshooting activities in processing issues.

Job 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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose Statement:

Support all API manufacturing activities to deliver to the business production plan, while meeting quality and safety compliance. Identify and drive production productivity improvement through yield improvement, waste and cycle-time reduction.

Major Responsibilities:

• Accountable for the continuous improvement activities/initiative for the manufacturing department.
• Develop and enhance capacity model, implement programs and reporting to improve production efficiency.
• Liaise with Tech Ops and Engineering to ensure the design of appropriate process fit in order to facilitate the introduction of new products.
• Work with all the support function to facilitate any trouble shooting activities resulting in timely closure of investigation and CAPA.
• Communicate effectively company policies, objectives and results as appropriate.
• Ensure accountability and commitment in achieving the goals of continuous improvement of EHS performance and maintaining legal compliance through active participation in AbbVie EHS programs.
• Review and update manufacturing documentation to meet cGMP and safety compliance.
• Identify areas for process, operator training and operational streamlining. Be involved in continuous Improvement (CI) projects.
• Oversee in all troubleshooting activities in processing issues, deviations and coordinating with other functions when required immediate and preventive actions.

Qualifications

• Bachelor Degree in Engineering (Chemical/ Pharmaceutical Engineering) or equivalent technical Degree. Master Degree desired but not required.
• Minimum of 5 years of pharmaceutical manufacturing experience.
• Able to work comfortably in 12-hour rotating shift (Day/Night)
• Ability to quickly know products and processes in order to assess performance issues.
• Demonstrates the highest levels of integrity and a strong work ethic.
• Proficiency in Delta V and MES
• Good knowledge of GxP requirements and regulations.
• Good level of decision making and problem solving.
• Good planning and scheduling skills.
• Good communication skills both verbal and written.
• Good interpersonal skills.

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