NordsonBoyle, 35 km from Sligo
Nordson Medical*, a global leader in the medical device industry, is seeking an experienced and highly motivated individual to join our team in *Boyle*, Ireland as a *NPI Engineer*. We are committed to creating a diverse and inclusive workplace...
Sligo
CQV Engineer (Process Equipment)
Team Horizon is seeking a CQV Engineer (Process Equipment) for a high-value expansion pharmaceutical in the North-West. In this role the CQV Engineer will be responsible for all aspects of the process equipment...
Sligo
Team Horizon is seeking a Validation Engineer on a permanent basis for our client’s manufacturing facility in the Northwest.
Why you should apply:
• You will get the opportunity to coordinate, implement and actively participate in the site...
Team HorizonSligo
Senior Project Engineers - Process Equipment
Senior Project Engineers - Biologics Process Equipment
Team Horizon is seeking a Senior Project Engineers - Biologics Process Equipment for a leading pharmaceutical company in Sligo.
Why you should...
Team HorizonSligo
CQV Engineer (Process Equipment)
Team Horizon is seeking a CQV Engineer (Process Equipment) for a high-value expansion pharmaceutical in the North-West. In this role the CQV Engineer will be responsible for all aspects of the process equipment...
Team HorizonCounty Sligo
CQV Engineer (Process Equipment)Team Horizon is seeking a CQV Engineer (Process Equipment) for a high-value expansion pharmaceutical in the North-West. In this role the CQV Engineer will be responsible for all aspects of the process equipment package, involved in the entire project lifecyle from des...
Team HorizonCounty Sligo
Senior Project Engineers - Biologics Process EquipmentTeam Horizon is seeking a Senior Project Engineers - Biologics Process Equipment for a leading pharmaceutical company in Sligo. Lead your regular weekly / bi-weekly Project review meetings with your Project team.
Liaise with Senior Engineering Ma...
Headcount Solutions LimitedSligo
ESSENTIAL Requirements * Degree in a relevant Engineering Discipline (Mechanical/Chemical/Process) * 5 years + strong site experience in API Manufacturing / OSD Manufacturing / BioPharm but will consider more junior (3 years) if they have relevant project site experience.
Experience in process eng...
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Quality Manufacturing Supervisor / Front Line Leader
Abbott Laboratories | Sligo | www.jobs.abbott |
About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Our 113,000 colleagues serve people in more than 160 countries.
Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs over 5,000 people across ten sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo.
Abbott has commercial, support operations and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
Abbott Ireland Nutrition Sligo
We understand that proper nutrition is the foundation for living the best life possible. That’s why we develop science-based nutrition products for people of all ages. Our products help babies and children grow, keep bodies strong and active, and support the unique nutrition needs of people with chronic illnesses — to make every stage of life a healthy one.
Abbott is a leader in providing enteral nutrition feeding devices, including enteral feeding pumps and pump sets. Enteral feeding (also known as tube feeding) is a means of providing nutrition to people who cannot obtain nutrition by swallowing.
Enteral nutrition contains all the calories and vitamins a person needs
Primary Function / Goals / Objectives
As Quality Manufacturing Supervisor / Front Line Leader, you will be reporting to the Site Quality Director with responsibility for maintaining the site quality system in compliance with all applicable quality system standards and regulations as well as Abbott policies and procedures.
Major Responsibilities
• Documenting and establishing a Quality System which assures compliance with them requirements of I.S. EN ISO 13485, EC Directive (93/42/EEC), MDR (2017/745) and Abbott Corporate and International Quality Policies and Procedures.
• Establishment of procedures and plans that define those elements necessary to meet regulatory, business and customer requirements.
• Ensure that quality procedures and instructions are understood, implemented, maintained and accessible to the appropriate personnel.
• Liaison with Abbott Nutrition Quality Assurance and regulatory authorities bodies.
• Ensure all manufactured products meet the requirements of regulatory authorities, end users and Abbott.
• Responsibility for measuring performance of the Quality System and providing metrics for management review meetings, monthly reports etc and at other frequencies as defined in relevant quality system procedures.
• Monitoring quality performance and advising management personnel on major quality issues
• Ensure management are kept informed of all system failures on a regular basis to ensure corrective or preventive action is undertaken where required.
• Supervision of relevant quality personnel.
• Review and approval of change control / validation packages.
• Coordination of product actions (recall, withdrawal or stock recovery) from the marketplace, where required.
• Tracking and Trending of Pest activity for the site on a monthly basis and implementing corrective and preventive action when required.
Supervisory/Management Responsibilities:
• The position has responsibility for managing several direct reports in the Quality Department.
Additionally, the position will require a role in the following areas:
• Frequent contacts with Abbott personnel at many levels, Division, Affiliate and other plants.
• Close contact with plant personnel at all levels.
EHS Responsibilities:
• Ensure Environmental Health & Safety standards are met and all EHS regulations and procedures are adhered to. Foster an awareness of Environmental Health & Safety in the plant and promote a culture of continuous improvement.
• Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Abbott’s EHS Program
• Ensure employees report any work-related injuries or illness to employee health and are promptly investigated
• Active participation and support of Abbott’s EHS programs
• Attend EHS training assigned and ensure that employees who report to you attend required training
• Investigate all employee-related H&S incidents, spills, releases to the environment and near misses, provide follow-up of corrective actions and ensure close-out
• Conduct staff meetings in which EHS is part of the agenda at least once per month.
Education Required:
• Diploma / Degree in a Quality Related, Engineering or Business-related discipline.
Knowledge/Experience:
• A minimum of 6 years relevant work experience at least 2 of which in a regulated manufacturing environment.
• Previous experience in Team Management a distinct advantage.
• Excellent communication skills.
• Strong Team building skills.
• Enthusiastic and energetic with the ability to integrate quickly into a team environment.
• Demonstrated flexible and innovative approach to work.
Accountability / Scope
• The position impacts directly on product quality and thus the financial and regulatory exposure of decisions could be significant.
• The position has scope for decision making within confines of agreed responsibilities. Activities broadly defined by agreed impact goals. Supervision is received through meetings and one on one meeting with the Quality Assurance Director. Periodic goal reviews, annual performance and career development reviews will also occur.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Our 113,000 colleagues serve people in more than 160 countries.
Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs over 5,000 people across ten sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo.
Abbott has commercial, support operations and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
Abbott Ireland Nutrition Sligo
We understand that proper nutrition is the foundation for living the best life possible. That’s why we develop science-based nutrition products for people of all ages. Our products help babies and children grow, keep bodies strong and active, and support the unique nutrition needs of people with chronic illnesses — to make every stage of life a healthy one.
Abbott is a leader in providing enteral nutrition feeding devices, including enteral feeding pumps and pump sets. Enteral feeding (also known as tube feeding) is a means of providing nutrition to people who cannot obtain nutrition by swallowing.
Enteral nutrition contains all the calories and vitamins a person needs
Primary Function / Goals / Objectives
As Quality Manufacturing Supervisor / Front Line Leader, you will be reporting to the Site Quality Director with responsibility for maintaining the site quality system in compliance with all applicable quality system standards and regulations as well as Abbott policies and procedures.
Major Responsibilities
• Documenting and establishing a Quality System which assures compliance with them requirements of I.S. EN ISO 13485, EC Directive (93/42/EEC), MDR (2017/745) and Abbott Corporate and International Quality Policies and Procedures.
• Establishment of procedures and plans that define those elements necessary to meet regulatory, business and customer requirements.
• Ensure that quality procedures and instructions are understood, implemented, maintained and accessible to the appropriate personnel.
• Liaison with Abbott Nutrition Quality Assurance and regulatory authorities bodies.
• Ensure all manufactured products meet the requirements of regulatory authorities, end users and Abbott.
• Responsibility for measuring performance of the Quality System and providing metrics for management review meetings, monthly reports etc and at other frequencies as defined in relevant quality system procedures.
• Monitoring quality performance and advising management personnel on major quality issues
• Ensure management are kept informed of all system failures on a regular basis to ensure corrective or preventive action is undertaken where required.
• Supervision of relevant quality personnel.
• Review and approval of change control / validation packages.
• Coordination of product actions (recall, withdrawal or stock recovery) from the marketplace, where required.
• Tracking and Trending of Pest activity for the site on a monthly basis and implementing corrective and preventive action when required.
Supervisory/Management Responsibilities:
• The position has responsibility for managing several direct reports in the Quality Department.
Additionally, the position will require a role in the following areas:
• Frequent contacts with Abbott personnel at many levels, Division, Affiliate and other plants.
• Close contact with plant personnel at all levels.
EHS Responsibilities:
• Ensure Environmental Health & Safety standards are met and all EHS regulations and procedures are adhered to. Foster an awareness of Environmental Health & Safety in the plant and promote a culture of continuous improvement.
• Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Abbott’s EHS Program
• Ensure employees report any work-related injuries or illness to employee health and are promptly investigated
• Active participation and support of Abbott’s EHS programs
• Attend EHS training assigned and ensure that employees who report to you attend required training
• Investigate all employee-related H&S incidents, spills, releases to the environment and near misses, provide follow-up of corrective actions and ensure close-out
• Conduct staff meetings in which EHS is part of the agenda at least once per month.
Education Required:
• Diploma / Degree in a Quality Related, Engineering or Business-related discipline.
Knowledge/Experience:
• A minimum of 6 years relevant work experience at least 2 of which in a regulated manufacturing environment.
• Previous experience in Team Management a distinct advantage.
• Excellent communication skills.
• Strong Team building skills.
• Enthusiastic and energetic with the ability to integrate quickly into a team environment.
• Demonstrated flexible and innovative approach to work.
Accountability / Scope
• The position impacts directly on product quality and thus the financial and regulatory exposure of decisions could be significant.
• The position has scope for decision making within confines of agreed responsibilities. Activities broadly defined by agreed impact goals. Supervision is received through meetings and one on one meeting with the Quality Assurance Director. Periodic goal reviews, annual performance and career development reviews will also occur.