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 documentations 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 require 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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 t...
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 documentations 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 require 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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