Maintenance Shift Supervisor
Team Horizon is seeking a skilled Maintenance Shift Supervisor to support the day-to-day maintenance requirements of Manufacturing Operations. This position reports to the Associate Director, Maintenance and has circa. 8 direct reports.
About the Role
The successful candidate will lead and manage a team of engineers and technicians to ensure the continuity and effectiveness of manufacturing. They will work Monday to Friday, from 4pm to 12 midnight.
Why You Should Apply
* This is an excellent opportunity to join a world-class manufacturing operation with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
* There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people's lives.
* Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
Key Responsibilities
* Responsible for continuity across shifts, throughout the week, including handovers.
* Responsible for timecard review and approval for all PSEs.
* Ensure adherence to training schedule, delivery of toolbox talks, WO coordination, WO reviews.
* Complete weekly review of PH sheets for accuracy and completeness.
* Arrange shift cover for A/L, approval of A/L requests.
* Set goals, performance management and development of all direct reports.
* Input to weekly planning meeting.
* Represent Engineering shift support at meetings.
* Resolve manufacturing escalations in a timely manner.
* Coordinate resources including outside contractors/services engineers and commissioning engineers, division equipment engineers etc.
* Work closely with Technical Shift Leaders/Operation Supervisors to ensure interdepartmental activities are planned and executed safely.
* Responsible for engineering compliance with all safety, environmental and quality related BOPs.
* Adhere to and follow all procedures policies and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines.
* Documentation of all activities in line with cGMP requirements.
* Cross train within the team and train new team members.
* Maintain the overall cGMP of the pharmaceutical processing areas.
* Build an ethos of Right First Time.
* And any other duties as assigned.
Requirements
* Diploma/Trade qualification in suitable science/engineering course and/or suitable experience.
* A minimum of 3 years' experience in a highly regulated industry in a similar role.
* Detailed functional knowledge of a wide range of manufacturing equipment is required.
* Proven instrumentation/troubleshooting ability.
* Strong interpersonal skills are essential as you will interact with external vendors, auditors, inspectors and other external parties.