Shift Production Supervisor
FRS Recruitment
Togher, Cork
We are seeking a Shift Production Supervisor for our client that operate in the waste recycling sector. Located on the South side of Cork city, the role of the Shift Production Supervisor is to manage the shift and the staff on the shift.
Reporting to the Operations Manager you will ensure the smooth running of the production process and that all products are produced to the specified quality and specifications. You will ensure all target and deadlines are met and that all staff complies with the company's Health and Safety procedures
Shift pattern: 2 x 12 hours weekends or weekends + 3 x days/evening shift
With direct reports such as Line Operators, Team Leaders, Machine Operators and Yard Operators your responsibilities will include the following:-
Key Responsibilities
º To take responsibility of the shift in terms of management of staff, management of production and quality targets and to ensure the smooth running of the production processes
º Responsible for the quality of the product that is produced within the shift in line with the companies quality systems, processes and procedures
º Monitor, measure and report on production related process performance and maintenance issues
º Ensure good communication is given verbally or written to all staff members
º Ensure that Health and Safety rules and regulations are adhered to during the shifts. Carry out regular Health and Safety meeting with safety reps.
º Problem solving and troubling shooting skills are used to ensure that all team members can identify root causes and take fast effective action to resolve the problems in hand
º Work closely with other Team Leaders/Supervisors to ensure smooth production handovers
º Identify and ensure that training skills are met for current and future shifts
º Maintain housekeeping standards to ensure a clean and safe workplace
º Be able to make appropriate decisions while following the company's organisational structure
º Maintaining and record a high level of timekeeping and non- absenteeism across all shifts
º Cary out "return to work interviews" following illness or non-appearance.
º Report and document any injury or "near miss" incident in the work place.
We are seeking candidates that have previously managed staff, working at a Team Leader level and who aspire to progress their career. If you can prove what it takes to be successful in this role, my client will reward you accordingly.
Manufacturing Production Supervisor (Shift)
Tandem Project Management
Dublin, DublinSummary:
Our client, a Global Life Science company in North Dublin, is seeking to recruit a 4 cycle (24/7) Manufacturing Production Supervisor (non- unionised position) to join the Manufacturing Operations Department. Reporting to the Shift Manager, the successful candidate will be responsible for ensuring the Process area operates in safe and GMP compliant manner at all times. The incumbent will manage a team of process chemists and/or chemical process operators.
Responsibilities:
- The role will be to build upon and improve existing process design to optimize process, facility and equipment use while conforming to SOPs and cGMP requirements.
- Lead and develop the team, to ensure safe and timely completion of all process activities according to cGMP's.
- Coordinate the workload of your team in order to meet schedules and timelines.
- Lead any Safety Investigations from your area identify and implement CAPA's.
- Mentor and coach your team in order to drive full performance and development.
- Set performance goals and objectives for team, and conduct performance appraisals.
- Work with the Shift Team Leads/Shift Manager (Shift Leadership Team) and track area progress on key issues.
- Drive Shift Metrics for your team.
- Fully Support all New Product Introduction (NPI) activities, to ensure Right First Time introduction of new products.
- Participate in and attend cross-functional (multidiscipline) meetings.
- Lead project-related working groups (cross-functional) in order continuously improve process and performance, with specific focus on Human Error reduction.
- Involved in recruitment and development of team.
- Lead investigations and corrective action follow-up to ensure closure of events/investigations in line with department metrics.
- Act as interface between management team and functional team.
- Assist with the creation and maintenance of area SOPs and validation documents for equipment and procedures, and assist in the writing of area status reports, regulatory documents, and process descriptions.
- Drive implementation and embedding of Lean Tools in the area (Standard Work, 5S, Yellow Belt).
Qualifications & Experience:
- Relevant degree level qualification.
- 4 to 5 years of working experience in a GMP regulated manufacturing environment.
- API experience is required.
- Prior relevant team leadership experience in a regulated manufacturing operations environment.
- Working knowledge of production operations, scheduling, design, planning, etc.
- Knowledge of lean management systems.
- Previous experience defining and establishing policies and SOPs.
Excellent leadership, communication, and interpersonal skills. - An ability to work independently and as a member of a team in a dynamic, fast-paced and goal driven environment.
Production Manager
HRM Recruit
Cork, Cork
Our client is an innovative food manufacturer who heavily supplies both the Irish and UK markets. Due to their continued expansion, they require a Production Manager to join their Cork team.
The Position:
- You will lead and manage the production team and will be a member of the management team reporting to the plant manager.
- It is your responsibility to create a culture that drives safe and efficient production which meets the requirements for quality, delivery, and total costs within the production area.
- Monitor, deliver and report against Site Metrics and KPI's
- You must lead continuous improvements efforts through employee engagement to deliver improved results in efficiencies, quality, cost, safety, and delivery to get to the root cause of systemic issues.
- Creating and developing a high performing cross-functional team driven by developing talent, visible leadership and creating a supportive team-based culture.
- You will be compliant with the company Health & Safety Policy and Procedures in the Low Care Area and continue working to improve H&S. As well as with the company Quality/Hygiene Systems and GMP/BRC standards.
- It will be a focus for you to train and develop supervisors, line leaders and operators.
- Execution of the daily plan. Liaising with Planning Dept. to improve planning.
- Liaising with Maintenance Dept. to ensure machinery is kept in full working order, serviced correctly and operators are appropriately trained.
- Achieving minimal levels of waste.
The Person:
For this role you will need:
- 5+ years' experience in a similar position within the food or ingredients industry.
- A degree in a relevant field.
- Strong leadership capabilities.
- A passion for continuous improvement centred around food production.
To learn more about this role apply online or contact Cian Breheny on +353 1 6321866 for a confidential discussion.
Quality Supervisor Job Cork
FRS Recruitment
Cork, Cork
Our client, based in Cork city environs, requires an Electronics Quality Supervisor.
You will be working within a supportive quality team, and reporting into the Quality and Lean Manager.
Based in Cork for over 30 years this company have an excellent track record of retaining their staff and is continually investing in the growth and development of their people and many of their employees have gone on to further their education and skill set through company sponsored programs.
This role offers a fantastic opportunity to progress your career & the benefits package includes a generous salary, healthcare, life assurance, pension scheme & bonus scheme as well as extensive training and development.
Do you have a formal degree qualification? Electronics/Quality/Engineering?
Do you have 5 years experience working in quality in an Electronics production facility?
Have you worked in an EN9100 certified facility, working on IPC610 and JSTD001 standards?
The Quality Inspection Supervisor is responsible for the leadership and development of the team, and for promoting best quality inspection practices in line with the company's strategy, goals and objectives.
The Quality Inspection Supervisor is responsible for effective and efficient management of quality inspection tasks, understanding and prioritising customers and programme's needs and for positive and constructive collaboration across different departments.
Specific Responsibilities:
- Inspection planning for incoming inspection
- Inspection planning for outgoing inspection of circuit card assemblies
- Inspection planning for outgoing inspection of system assemblies
- Inspection planning for outgoing inspection of aftermarket products
- Review of customer quality requirements
- Implementation and verification of customer quality requirements
- First Article Inspection
- Reporting and analysis of internal product related quality issues
- Internal yield measurements and analysis of data
- Reporting on quality performance / KPIs
- Support to continuous improvement and LEAN activities
If you would like to hear more about this exciting new job opportunity, please apply today by sending your cv.
Please note, you need to be in Ireland, and eligible to work in Ireland without a work visa.
CONSULTANT: MANDY DEVLIN 086 410 6852
You may have also searched for Quality Jobs Cork, Quality Engineer jobs Cork, Quality Supervisor Jobs Cork, Quality jobs Ireland, Quality Electronics jobs, Electronics Quality jobs Cork
Engineering Manager
SensL
CorkSensL is the leading provider of low light sensors based on its solid-state single photon avalanche diode (SPAD) and silicon photomultiplier (SiPM) technology. SensL has pioneered the production of its sensor technology in high volume, industry standard, CMOS fabrication facilities delivering unprecedented performance, uniformity, quality, reliability and low cost. SensL provides the ideal candidate with a unique opportunity to work with a profitable, growing, high tech company involved in the latest technology trends such as self-driving autonomous vehicles, cancer detection and cloud based radiation detection.
The Engineering Manager will have responsibility for the on-time delivery of new SensL products and the on-time shipment of existing products to customer.
Key Responsibilities
- Manage engineering product development phases from concept to mass production
- Lead product development through effective management of engineering resources
- Identify and develop risk mitigation plans for key risk items critical to the delivery of SensL products
- Run weekly engineering team meetings
- Report product development status at weekly management meetings
- Manage SensLs supply chain working with the key engineers responsible for each outsourced contract manufacture
- Responsible for ensuring contract manufactures adhere to SensL quality standards
Experience and skills required
- Proven ability to lead a multi-disciplinary engineering team
- Expert level project management skills
- Experience working with and managing outsource vendors
- Excellent communication and planning skills
- Ability to interact with senior management and concisely convey complex information regarding program and operations status
- High level Engineering degree
Benefits
This position is at the Engineering Manager level and carries an attractive salary, stock options, health coverage and employer pension contribution. This position is full time and based at SensLs corporate headquarters in Cork, Ireland.
Packaging Team Leader/Manager
Aerie Pharmaceuticals
Ireland, WeThe 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.
Senior Engineering Manager
Medtronic
IrelandDescription
OUR PURPOSE
At our Research & Development Department in Medtronic, plc, we focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Our Engineers are directly involved in the development of innovative products for use in medical procedures. The Senior R&D Manager is directly involved in providing high level leadership and direction to a diverse R&D team ensuring the implementation of strategic and tactical R&D activities.
Qualifications
FURTHER, TOGETHER
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations.OUR PURPOSE
At our Research & Development Department in Medtronic, plc, we focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Our Engineers are directly involved in the development of innovative products for use in medical procedures. The Senior R&D Manager is directly involved in providing high level leadership and direction to a diverse R&D team ensuring the implementation of strategic and tactical R&D activities.
The CVG Division has a unique opportunity for the right candidate to take their place amongst the leadership team and help shape the direction of modern interventional treatment within one of the fastest growing businesses in medical devices, an are in which Medtronic is a market leader. You will have the opportunity to guide engineering innovation at the forefront of interventional treatment, developing never before seen devices and more.
Careers that Change Lives
A Day in the Life
A Day in the Life
Responsibilities may include the following and other duties may be assigned.
- Plans, directs and implements all aspects of the company's design and development of new medical device products or software systems.
- May develop, evaluate, implement and maintain technical quality assurance and control systems or reliability systems and standards pertaining to materials, techniques, or company products.
- Oversees the investigation and evaluation of existing technologies.
- Guides the conceptualization of new methodologies, materials, machines, processes or products.
- Directs the development of new concepts from initial design to market release.
- Manages feasibility studies of the design to determine if capable of functioning as intended.
- Monitors documentation maintenance throughout all phases of research and development.
- Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
- Selects, develops and evaluates personnel to ensure the efficient operation of the function.
Qualifications
Must Have: Minimum Requirements
• We are looking for a qualified person to Level 8 Degree in Engineering / Science or related discipline, Masters preferred and desirably with 10 years relevant direct engineering experience within medical device environment.
• A minimum of three to five years direct managerial experience of engineers and a career history of demonstrated progressive management experience.
• Dynamic team player and leader and can work effectively and proactively on cross-functional teams.
• Experienced in a medical device market and have a proven result driven track record.
• Excellent team building, communication, people management and leadership skills are desirable.
• Good communicator and fluent in English, both in writing and speaking.
Nice to Have
About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
EMEA-IrelandNice to Have
About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
No More Results
Job Type
Full Time
Posted
Today
Description
We are seeking a Shift Production Supervisor for our client that operate in the waste recycling sector. Located on the South side of Cork city, the role of the Shift Production Supervisor is to manage the shift and the staff on the shift.
Reporting to the Operations Manager you will ensure the smooth running of the production process and that all products are produced to the specified quality and specifications. You will ensure all target and deadlines are met and that all staff complies with the company's Health and Safety procedures
Shift pattern: 2 x 12 hours weekends or weekends + 3 x days/evening shift
With direct reports such as Line Operators, Team Leaders, Machine Operators and Yard Operators your responsibilities will include the following:-
Key Responsibilities
º To take responsibility of the shift in terms of management of staff, management of production and quality targets and to ensure the smooth running of the production processes
º Responsible for the quality of the product that is produced within the shift in line with the companies quality systems, processes and procedures
º Monitor, measure and report on production related process performance and maintenance issues
º Ensure good communication is given verbally or written to all staff members
º Ensure that Health and Safety rules and regulations are adhered to during the shifts. Carry out regular Health and Safety meeting with safety reps.
º Problem solving and troubling shooting skills are used to ensure that all team members can identify root causes and take fast effective action to resolve the problems in hand
º Work closely with other Team Leaders/Supervisors to ensure smooth production handovers
º Identify and ensure that training skills are met for current and future shifts
º Maintain housekeeping standards to ensure a clean and safe workplace
º Be able to make appropriate decisions while following the company's organisational structure
º Maintaining and record a high level of timekeeping and non- absenteeism across all shifts
º Cary out "return to work interviews" following illness or non-appearance.
º Report and document any injury or "near miss" incident in the work place.
We are seeking candidates that have previously managed staff, working at a Team Leader level and who aspire to progress their career. If you can prove what it takes to be successful in this role, my client will reward you accordingly.