Operational and Technical
- Responsible for of batch manufacturing and changeover cleaning instructions in accordance with predefined procedures and training.
- Ensures batch is performed with adherence process critical steps and ensures flawless
- Provides inputs on operational and process related improvements to achieve site business targets and manufacturing excellence.
- Performs technical verification of batch related recipes (POMS and DeltaV) manual operations and adhoc manufacturing documentations
- Able to perform basic operational and process related troubleshooting and coordinate with other cross functions where required
- Tasked with preparing and cleaning equipment for pre and post maintenance related work
- Provides input in design of manufacturing recipe in DCS
- Make sure shift duties are communicated and handed over properly.
- Participate in digitalization projects and identify areas for process and operational streamlining.
Safety
- Adheres to safe work environment in accordance with regulatory and global/local EHS policies.
- Be part of the site Emergency Response Team.
- Participates in safety risks assessments or participates in process hazard analysis as an operations representative(PHA).
Quality
- Actively resolve batch related document errors in a timely manner.
- Communicates all events/issues effectively with relevant stakeholders.
- Ensure all documentation is completed in accordance with GMP and GDP guidelines.
- Provide inputs for investigation impact assessment and appropriate CAPA.
- Ensures overall plant upkeep during the shift and ensuring plant is always in audit ready mode.
- Fulfill all necessary training requirements by participating in scheduled sessions computerbased training (CBT) onthejob training (OJT) job safety analysis (JSA) and by reading and comprehending relevant materials.
Schedule
- Oversees deliverables ahead anticipates complexities and prevents potential delays.
- Ensures processes are running as per planned schedule with minimal delays. Highlights effectively to shift supervisor if delays are expected.
Qualifications :
- Diploma in Chemical Engineering/ Pharmaceutical Science or equivalent technical related diploma is required.
- At least 6 years of experience in working in a GMP manufacturing environment.
- Proficient in using DeltaV distributed control systems.
- Experience in using MES systems in batch and raw material consumption.
- Able to work comfortably in 12hour rotating shift (Day/Night).
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.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Fulltime