Manufacturing Process Engineer
Manufacturing Process Engineer
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Job Description
We are looking for a Manufacturing Process Engineer to join our Engineering Team in Abbvie Westport. This position reports to the Associate Director of Pharma Maintenance. The successful candidate provides technical assistance for equipment/machinery and all aspects of performance around the manufacturing and aseptic filling of AbbVie products to customer requirements FDA HPRA EPA and safety standards within budget parameters. You need to have active communication and engagement with many stakeholders within the business (i.e. E&T Validations QA Vendors Contractors etc. to achieve the Site goals.
Roles and Responsibilities
- Assist with management engineering process improvement equipment reliability and control system activities.
- Identify plan schedule manage and communicate on production related projects to all affected stakeholders.
- Implement lean technologies such as standard work visualisation boards.
- Support the business by developing robust process & systems to ensure delivery of effective quality.
- Ensure that line processes equipment and materials are maintained to deliver consistent reliable and predictable process performance and product quality.
- Develop & implement systems & structure to minimise technical downtime on the line.
- Resolve and lead technical issues in an effective & timely manner with the technical team to support operations.
- Drive continuous improvement and process efficiency programs i.e. MEP OEE OPEX RCA RCM and productivity output for the business.
- Manage external vendors and services for equipment and technology
- Manage the technical documentation reports files logs and records for the department.
- Assist with the trending monitoring performance of equipment and the reduction of unplanned downtime.
- Help manage track and monitor the relevant KPIs for the Technical Team.
- Assist with the trending monitoring and reduction of repeat deviations associated with the equipment and technology. Generate and approve associated change controls and relevant protocols.
- Help support the BU during regulatory and compliance audits.
- Become an SME for the Aseptic Fill and Packaging operations equipment
Qualifications :
- Degree in Mechanical Electrical or Process Engineering
- 4 years experience working in a regulated environment (Pharmaceutical/Medical Device).
- Detailed knowledge of regulatory requirements in a pharmaceutical GxP environment.
- Computer literate with experience of: Maximo SAP Trackwise and working with Microsoft Office (Word Excel PowerPoint etc..
- Strong ability to evaluate diagnose and troubleshoot problems.
- Flexibility to respond to issues outside normal business hours.
- Ability to learn new and different technologies.
- Experience in high volume automation Pharmaceutical manufacturing environment.
- Ability to organize workload and work on own initiative.
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:
No
Employment Type :
Fulltime
Employment Type
Full-time
