API Maintenance Lead

Sligo - Ireland

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

We have an exciting opportunity for a Maintenance Lead to join our engineering team in Sligo. This position reports to the Drug Product Engineering Manager. The successful candidate will lead and manage a team of plant support engineers and technicians to support manufacturing continuously efficiently and effectively.

Roles and Responsibilities

Ensure continuity across shifts throughout the week including a.m. handovers.
Complete timecard review and approval for all PSEs.
Responsible for adherence to training schedule delivery of toolbox talks WO coordination WO reviews.
Complete weekly review/accuracy/completeness of PH sheets.
Arrange shift cover for Annual Leave approve Annual Leave and other requests.
Set goal manage performance and development activities for all direct reports.
Input to weekly planning meeting.
Represent Engineering shift support at Tier 1 morning meetings.
Resolve manufacturing escalations in a timely manner.
Coordinate resources and assign tasks and activities.
Work closely with Technical Shift Leaders/Operation Supervisors to ensure interdepartmental activities are planned and executed safely.
Ensure Engineering compliance with all safety environmental and quality related BOPs.
Document all activities in line with cGMP requirements.
Cross train team members and train new team members.
Maintain the overall cGMP of the pharmaceutical processing areas.

Qualifications :

Diploma/Trade qualification in suitable science/engineering course and/or suitable experience.
3 years experience in a highly regulated industry performing an equivalent position.
Detailed functional knowledge required of a wide range of manufacturing equipment is essential.
Proven instrumentation/troubleshooting ability.
Good knowledge of procedures policies and guidelines required to comply with cGMP and HPRA/FDA guidelines.
Must be flexible and support the business through working shift and adhering to the standby schedule.

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 :

Employment Type :

Full-time

We have an exciting opportunity for a Maintenance Lead to join our engineering team in Sligo. This position reports to the Drug Product Engineering Manager. The successful candidate will lead and manage a team of plant support engineers and technicians to support manufacturing continuously efficient...

Roles and Responsibilities

Ensure continuity across shifts throughout the week including a.m. handovers.
Complete timecard review and approval for all PSEs.
Responsible for adherence to training schedule delivery of toolbox talks WO coordination WO reviews.
Complete weekly review/accuracy/completeness of PH sheets.
Arrange shift cover for Annual Leave approve Annual Leave and other requests.
Set goal manage performance and development activities for all direct reports.
Input to weekly planning meeting.
Represent Engineering shift support at Tier 1 morning meetings.
Resolve manufacturing escalations in a timely manner.
Coordinate resources and assign tasks and activities.
Work closely with Technical Shift Leaders/Operation Supervisors to ensure interdepartmental activities are planned and executed safely.
Ensure Engineering compliance with all safety environmental and quality related BOPs.
Document all activities in line with cGMP requirements.
Cross train team members and train new team members.
Maintain the overall cGMP of the pharmaceutical processing areas.

Qualifications :

Diploma/Trade qualification in suitable science/engineering course and/or suitable experience.
3 years experience in a highly regulated industry performing an equivalent position.
Detailed functional knowledge required of a wide range of manufacturing equipment is essential.
Proven instrumentation/troubleshooting ability.
Good knowledge of procedures policies and guidelines required to comply with cGMP and HPRA/FDA guidelines.
Must be flexible and support the business through working shift and adhering to the standby schedule.

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 :

Employment Type :

Full-time

Key Skills

Graduate Engineering
Corporate Risk Management
Adobe Photoshop
Big Data
Clinical
Asic

Apply Now

About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

View Profile View Profile

AI AutoApply

Apply to 100+ jobs with one click