production supervisor jobs

Near limerick, limerick
6Jobs Found

6 jobs found for production supervisor jobs Near limerick, limerick

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Production Supervisor

Microchip

Ennis
5 days ago
Ennis
5 days ago

Company Description

Microchip Technology Inc. is a leading provider of embedded control applications. Our product portfolio comprises general purpose and specialized 8-bit, 16-bit, and 32-bit microcontrollers, 32-bit microprocessors, field-programmable gate array (FPGA) products, a broad spectrum of high-performance linear, mixed-signal, power management, thermal management, radio frequency (RF), timing, safety, security, wired connectivity and wireless connectivity devices, as well as serial Electrically Erasable Programmable Read Only Memory (EEPROM), Serial Flash memories, Parallel Flash memories, and serial Static Random Access Memory (SRAM). We also license Flash-IP solutions that are incorporated in a broad range of products.

Job Description

Job Description: 

As production supervisor you will work with the Production Manager and a team of Supervisors and Production Specialists with other cross functional teams to achieve business goals in a busy high- volume production facility.

Responsibilities:

  • Responsible for managing and controlling resources to ensure production areas achieve the production plan while maintaining safety, quality, service and cost controls in place for the production line.
  • Regularly hold team meetings and line meetings.
  • Complete 1:1 performance reviews with operators on a quarterly basis.
  • Responsible for meeting production Plans & Schedules as agreed with the Production Control Department and Production Manager.
  • Be capable of leading and guiding the cross functional teams in providing permanent solutions to technical / quality issues.
  • Engage with all employees to foster teamwork ensuring everyone contributes to their full potential in pursuit of organizational objectives.
  • Maintain and foster a safe workplace environment.
  • Develop systems and procedures for continuous improvements utilizing lean tools, systems, procedures and techniques to drive continuous improvements across the production department and plant.
  • Report performance against agreed metrics
  • Drive practical problem-solving activity in order to meet all key performance metrics. Collaborating with key groups and stakeholders to conduct root cause analysis and eliminate re work.
  • Ensure compliance to regulatory requirements at all times. AS9100/ISO14001.
  • Understand and fully implement Microchip’s Guiding Values
  • Implement and monitor operational efficiencies throughout the production processes.

Job Requirements

Qualifications/Experience Required:

  • Education and experience equivalent to a related Diploma/Degree in Business Management or equivalent.
  • A minimum of 3 years experience of leading/managing people, preferably in a manufacturing environment.
  • Excellent communications skills, both written and verbal. Ability to communicate effectively with own team, other functions and the management team.
  • Action oriented and enjoys a challenge: drives for results: is versatile, flexible and is willing to work within constantly changing priorities with enthusiasm
  • Team player and ability to work on own initiative.
  • Excellent analytical skills, including the ability to identify improvements in manufacturing methods and processes.
  • Strong understanding of the pressures associated in leading a production team.

 

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Production Supervisor

Cook Group

Limerick
30+ days ago
Limerick
30+ days ago

The primary purpose of this position is to lead a team of QC Manufacturing Team Members in a production environment.

 

Reporting to: Quality Control Manager  

 

 

Find out more about Cook Medical here


  • Responsible for Quality Control of medical devices within Cook Medical including inspection of raw materials, in-process product, finished and sterilized devices.
  • Ensure that the work done by quality control personnel is in compliance with the requirements of the quality system.
  • Prepare or review SOP’s manufacturing/quality control instructions, which are required by the quality team.
  • Ensure that a high standard of cleanliness is maintained in the manufacturing areas in order to control product bio burden.
  • Ensure that changes to relevant procedures/instructions are relayed to those affected in production.
  • Ensure that training needs of employees in the QC area are constantly reviewed and that required training is given as appropriate.
  • Monitor employee performance and carry out performance appraisals with employees.
  • Maintain excellent communication channels with the production team and with other departments.
  • Work closely with other departments to meet delivery requirements.
  • Take ownership for assigned customer complaints, CAPA’s and determine root cause.
  • Monitor rejects from quality control processes and disposition through MRB process
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

  • Level 8 in Manufacturing Engineering or related discipline preferable.
  • Minimum 5 years previous experience in a supervisory position desirable.
  • Strong communication and inter-personal skills.
  • Knowledge of medical device quality standards ISO13485/FDA practices and GMP or similar regulated industry standards.
  • Knowledge of Lean Manufacturing desirable
  • Good computer skills including knowledge of Microsoft® Office.
  • Excellent organisational and team building skills.
  • High self-motivation.
  • Willingness and availability to travel on company business.

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Production Supervisor

Cook Group

Limerick
30+ days ago
Limerick
30+ days ago

Overview

The primary purpose of this position is to lead a team of QC Manufacturing Team Members in a production environment.

 

Reporting to: Quality Control Manager  

 

 

Find out more about Cook Medical here

Responsibilities

  • Responsible for Quality Control of medical devices within Cook Medical including inspection of raw materials, in-process product, finished and sterilized devices.
  • Ensure that the work done by quality control personnel is in compliance with the requirements of the quality system.
  • Prepare or review SOP’s manufacturing/quality control instructions, which are required by the quality team.
  • Ensure that a high standard of cleanliness is maintained in the manufacturing areas in order to control product bio burden.
  • Ensure that changes to relevant procedures/instructions are relayed to those affected in production.
  • Ensure that training needs of employees in the QC area are constantly reviewed and that required training is given as appropriate.
  • Monitor employee performance and carry out performance appraisals with employees.
  • Maintain excellent communication channels with the production team and with other departments.
  • Work closely with other departments to meet delivery requirements.
  • Take ownership for assigned customer complaints, CAPA’s and determine root cause.
  • Monitor rejects from quality control processes and disposition through MRB process
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

Qualifications

  • Level 8 in Manufacturing Engineering or related discipline preferable.
  • Minimum 5 years previous experience in a supervisory position desirable.
  • Strong communication and inter-personal skills.
  • Knowledge of medical device quality standards ISO13485/FDA practices and GMP or similar regulated industry standards.
  • Knowledge of Lean Manufacturing desirable
  • Good computer skills including knowledge of Microsoft® Office.
  • Excellent organisational and team building skills.
  • High self-motivation.
  • Willingness and availability to travel on company business.

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Production Supervisor

Edwards Lifesciences

Shannon
30+ days ago
Shannon
30+ days ago
The Company: Edwards Lifesciences is driven by a passion to help patients. The company collaborates with the world’s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives.
The Role : Supervise employees and activities across areas of production for smooth and continuous operations.
Key Responsibilities:
• Supervise employees and manufacturing activities pertaining to the production of products and/or manufacturing processes in - and with manufacturing/technical knowledge of - 2 or more production areas, depending on the complexity of the areas, in addition to conducting performance reviews, including resolving performance issues.
• Lead improvement projects, partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assures documentation content is valid
• Accountable for productivity and quality metrics of staff, and provide regular progress reports and manufacturing metrics to management and cross-functional stakeholders.
• Oversee the scheduling of work orders and team performance metrics.
• Ensure appropriate staffing for all positions.
• Accountable to ensure staff is appropriately trained to perform assigned work.
• Document owner for assigned product line assembly procedures
• Monitor raw material usage and availability required in daily production
• Monitor material and labor variances to meet established standards
• On time arrival to work, regular attendance without excessive absenteeism, and working a full 8 hour or longer work period
• Other incidental duties (e.g. occasional photo copying or deliveries)
Education and Experience:
Bachelor's Degree
2 years years experience previous related experience required with full responsibility for all personnel including hire/fire authority and handling all aspects of employee relations in manufacturing, quality and/or product development engineering
Experience working in multi-cultural teams with cultural sensitivity
Experience working in a medical device industry
Additional Skills:
• Project management experience
• Proven expertise in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system, preferably JDE
• Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives, as well as mediating differences to achieve consensus
• Full understanding of manufacturing procedures related to all stages of own area of responsibility
• Demonstrated ability to supervise teams and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations
• Ability to analyze and identify potential line/operation layouts adjustments to improve efficiency
• Full understanding of processes and equipment used in assigned work
• Ability to work and excel within a fast paced, dynamic, and constantly changing work environment
• Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
• Knowledge of Lean Manufacturing concepts and Six Sigma
• Supervise a section of production activity to accomplish tasks, projects and operations
• Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.
For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
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Quality Systems Supervisor

Edwards Lifesciences

Shannon
19 days ago
Shannon
19 days ago
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world’s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives.
Duties:
+ Supervise employees and quality activities pertaining to the change control process, training process and Analysis of Data, including Quality Data Review
+ Conduct performance reviews and resolve performance issues as needed
+ Oversee the assignment of ECR PCS review and initiation tasks and team performance metrics
+ Ensure appropriate staffing to support project and line support ECR activities at the Draper and Ireland sites
+ Oversee the assignment of tasks to the Training Team and QS Analyst
+ Accountable to ensure staff is appropriately trained to perform assigned work
+ Accountable for productivity and quality metrics of staff, and provide regular progress reports and quality metrics to management and cross-functional stakeholders
+ Partner with engineering and management team to set priorities of incoming work to meet business objectives
+ Communicate with corporate partners to ensure work aligns with procedural requirements
Requirements
+ Bachelors Degree
+ Minimum one years experience Supervising a Quality/Manufacturing team
+ Good computer skills in usage of MS Office Suite; Experience in ERP preferred
+ Excellent written and verbal communication skills and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives, as well as mediating differences to achieve consensus
+ Good problem-solving and critical thinking skills
+ Experience with project management and project management software tools preferred
+ Solid knowledge and understanding of Edwards policies, procedures, and regulatory (e.g., medical, pharmaceutical) guidelines relevant to documentation
+ Solid understanding of medical device documentation development activities, knowledge of ISO13485
+ Ability to manage confidential information with discretion
+ Ability to analyze and identify potential adjustments to improve efficiency
+ Demonstrated ability to supervise teams, provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to manage competing priorities in a fast paced environment
+ Must be able to work with cross-functional teams as well as with colleagues from other departments within assigned area
+ Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.
For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
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Packaging Team Leader/Manager

Aerie Pharmaceuticals

Ireland, We
28 days ago
Ireland, We
28 days ago
 
The Packaging Team Leader leads Aerie’s secondary packaging operations in Athlone through the completion of secondary packaging manufacturing activity.
 
Packaging operations involve high speed packaging of sterile eye drop bottles including brite stock packaging, finished packaging include labelling, cartoning, bundling, case packing and palletisation. The packaging team leader is also responsible for the resulting manufacturing batch records used to record manufacturing activity and to enable the release of product batches to the market.

Essential Duties, Functions and Responsibilities:
  • Works with manufacturing and quality colleagues as part of an Operation’s team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site.
  • Prioritises safety personally and within the team to ensure a safety first culture when operating equipment within packaging – champions safe working always.
  • Ensures focus on the quality performance of the packaging area to ensure system and human errors are minimised through SOP and MBR design and through daily focus on quality culture.
    • Leads the packaging area and the manufacture of products in accordance with the production schedule, BOMs and finished product specifications.
    • Coordinates manufacturing activity according to schedules agreed with Supply Chain and ensure engagement of support areas required to assist in packaging performance.
    • Monitors and reports on key area performance metrics across safety, quality, delivery and cost.
    • Leads the recruitment, training and performance management of the members of the Packaging manufacturing team.
    • Leads the packaging area in nurturing a continuous improvement culture and the deployment of appropriate lean ways of working to enable that continuous improve drive.
  • Lead Packaging Operations on the site’s New Product Introduction team.
    • Represent Packaging Operations as the manufacturing SME at regulatory audits and lead the area in preparing for these audits.
    • Provides manufacturing support for product PPRs (Periodic Product Review) from a Packaging perspective.
  • Ensures effective manufacturing investigation into deviations and process/equipment downtime.
  • Supports validation activity as required.
Aerie Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Skills/Knowledge Required: 
  • Strong knowledge of finished product packaging operations and track record leading in a high volume regulated environment.
    • Understanding of pharmaceutical industry regulatory requirements as they apply to packaging.
    • Strong leader of operations personnel with direct supervision experience.
    • Strong communication and interpersonal skills. Highly motivated with ability to work effectively with multidisciplinary teams.
    • Strong team player with proactive approach & manner.
Education Required:
  • Bachelor’s Degree in Science/Manufacturing/Engineering or equivalent.
Experience Required:
  • 5+ years relevant experience in a pharmaceutical manufacturing or similar environment with at least 3+ in a supervision/leadership capacity.
  • Demonstrated experience in managing the day-to-day activities of a packaging/manufacturing team.
  • Skilled at motivating a multifunctional team to achieve organizational goals.
  • Comfortable developing and implementing a timeline to achieve targets.
  • Demonstrated experience in managing performance, delegating tasks and coaching and training team members to maximize their potential.
 
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Posted

5 days ago

Description

Company Description

Microchip Technology Inc. is a leading provider of embedded control applications. Our product portfolio comprises general purpose and specialized 8-bit, 16-bit, and 32-bit microcontrollers, 32-bit microprocessors, field-programmable gate array (FPGA) products, a broad spectrum of high-performance linear, mixed-signal, power management, thermal management, radio frequency (RF), timing, safety, security, wired connectivity and wireless connectivity devices, as well as serial Electrically Erasable Programmable Read Only Memory (EEPROM), Serial Flash memories, Parallel Flash memories, and serial Static Random Access Memory (SRAM). We also license Flash-IP solutions that are incorporated in a broad range of products.

Job Description

Job Description: 

As production supervisor you will work with the Production Manager and a team of Supervisors and Production Specialists with other cross functional teams to achieve business goals in a busy high- volume production facility.

Responsibilities:

  • Responsible for managing and controlling resources to ensure production areas achieve the production plan while maintaining safety, quality, service and cost controls in place for the production line.
  • Regularly hold team meetings and line meetings.
  • Complete 1:1 performance reviews with operators on a quarterly basis.
  • Responsible for meeting production Plans & Schedules as agreed with the Production Control Department and Production Manager.
  • Be capable of leading and guiding the cross functional teams in providing permanent solutions to technical / quality issues.
  • Engage with all employees to foster teamwork ensuring everyone contributes to their full potential in pursuit of organizational objectives.
  • Maintain and foster a safe workplace environment.
  • Develop systems and procedures for continuous improvements utilizing lean tools, systems, procedures and techniques to drive continuous improvements across the production department and plant.
  • Report performance against agreed metrics
  • Drive practical problem-solving activity in order to meet all key performance metrics. Collaborating with key groups and stakeholders to conduct root cause analysis and eliminate re work.
  • Ensure compliance to regulatory requirements at all times. AS9100/ISO14001.
  • Understand and fully implement Microchip’s Guiding Values
  • Implement and monitor operational efficiencies throughout the production processes.

Job Requirements

Qualifications/Experience Required:

  • Education and experience equivalent to a related Diploma/Degree in Business Management or equivalent.
  • A minimum of 3 years experience of leading/managing people, preferably in a manufacturing environment.
  • Excellent communications skills, both written and verbal. Ability to communicate effectively with own team, other functions and the management team.
  • Action oriented and enjoys a challenge: drives for results: is versatile, flexible and is willing to work within constantly changing priorities with enthusiasm
  • Team player and ability to work on own initiative.
  • Excellent analytical skills, including the ability to identify improvements in manufacturing methods and processes.
  • Strong understanding of the pressures associated in leading a production team.

 

Source: Microchip