SEEKING A MACHINE SETTER FOR A **APPLY ON THE WEBSITE**-MONTH
FIXED-TERM CONTRACT TO COVER A VACANCY ON WEEKEND NIGHT SHIFT.
JOB TITLE MACHINE SETTER (WEEKEND DAY SHIFT 6.**APPLY ON THE WEBSITE**
PM - 6.**APPLY ON THE WEBSITE** AM
ROLE ACCOUNTABILITIES
This role will work across a number of areas, predominately cell 1,
with cover required for other areas when required.
KEY RESULT AREAS / KEY TASKS
* EHS
* Ensure compliance with and assist in the maintenance of a safe
company culture by working within relevant Company and Corporate
requirements and legislation governing environmental, health and
safety as principally contained in the Safety, Health and Welfare at
Work Act **Apply on the website**, Safety Cardinal Rules, Safety
Statement, etc. Report any equipment or process problems as
appropriate
* Ensure all machine safety guards are working.
* Highlight and work to eliminate unsafe methods/equipment/hazards
as appropriate.
* QUALITY
* Ensure quality in all aspects of work by following Standard
Operating Procedures (SOPs) and Standard Work Instructions (SWIs) and
maintaining compliance with all quality requirements.
* Set-up all machines as per relevant procedures.
* Ensure machines are set-up and run within validated parameters at
all times.
* Complete first-piece checks and all related paperwork. Ensure
product quality is to specification.
* Carry out on-line quality checks as per relevant procedures.
* Ensure equipment is set-up correctly 1st time to maximize quality
and minimize potential for defects.
* As the majority of work undertaken will take place in a clean-room
environment, GMP and 5S compliance is essential. Ensure equipment and
benches are cleaned after every set up and floors, storage areas, etc
are maintained to a high standard and take an active role in 5S
projects in your area
* MACHINERY
* Correct set-up, general maintenance and preventative maintenance
of production equipment.
* Ensure all equipment is set-up as per the relevant procedure and
parameter sheets.
* Troubleshoot mechanical problems and repair or replace parts as
appropriate.
* Ensure proper identification and storage of tools, gauges etc.
* Ensure equipment set-up is running within standard time and
produces **Apply on the website**% efficiency in order to achieve
associated OEE targets.
* Minimise downtime and work closely with Supervisors and
Engineering to ensure maximum utilization of equipment.
* Ensure set ups are completed in a timely manner and participate in
SMED projects, to continuously reduce set up times.
OTHER RESPONSIBILITIES WILL INCLUDE, BUT ARE NOT LIMITED TO, THE
FOLLOWING:
* Monitor scrap levels to ensure they do not exceed standard for any
operations and reduce defects off machines and thereby reduce scrap in
the plant.
* Identify process, equipment and documentation improvements where
possible and take part in improvement projects as assigned (e.g. Lean
Manufacturing/Six Sigma/SMED)
* Complete all identified training and development activities as
required including allocated MyLearning courses.
* Adhere strictly to company policies, procedures and plant key
behaviours as notified.
* Assist in the maintenance of a safe company culture by working
within the company**Apply on the website**;s environmental, health
and safety guidelines and Safety Cardinal Rules at all times. Report
any hazards, equipment or process issues in line with plant escalation
procedures
* Adhere to GMP based Quality Systems requirements for medical
devices and medicinal product (e.g. MDD, EU GMP Guidelines Vol IV Part
1 for medicinal product, ISO **Apply on the website**).
EXPERIENCE, QUALIFICATIONS AND SKILLS REQUIRED
* Education: Senior Trade / Recognised Mechanical / Plastics
qualification or Mechanical / Electrical Engineering Diploma
* Experience in an automated environment supporting high volume
mechanical / pneumatic manufacturing system is desirable
* Experience of automated equipment, PLCs, electro pneumatics,
servos, lubrication systems, preventative maintenance programmes.
* Experience in a high-volume manufacturing environment.
ESSENTIAL CRITERIA FOR THE POSITION ARE:
* Ability to articulate technical facts in a clear and concise manner
* Ability to work well in a team setting
* Self-starter, ability to use own initiative.
* Ability to take ownership for process, and drive troubleshooting
and improvement activities
* Ability to work under minimum supervision.
* Organised and resourceful with excellent attention to detail and
ability to get the job done
* Ability to multi-task and to work in a high paced environment with
an awareness of continued impact on production and the plant
performance.
* Ability to learn quickly and work on own initiative, under minimum
supervision
* Basic knowledge of mechanical, electrical and pneumatic components
* Quality awareness and a proven track record of excellent quality
standards
* Commitment to work within the ethos of the Medical Devices &
Supplies Guide to Compliance and Quality Manufacturing and the company
business conduct guidelines.
* Clear written and verbal communication skills
* Manufacturing process knowledge and experience
* Commitment to continuous improvements with the initiative and
ability to improve work processes
* An excellent standard of attendance and time keeping
* The ability to interact with employees at all levels of the
organisation and work as part of a team
Kelly Services are acting as an Employment Business in relation to
this role. Should you choose to apply, your information will be
processed in accordance with Kelly**Apply on the website**;s Privacy
Statement. For information regarding data protection at Kelly, please
visit the Kelly website and have a look into the Privacy Statement.
As an Equal Opportunities employer we welcome applications from all
suitably qualified persons regardless of their race, sex, disability,
religion/belief, sexual orientation or age.
DUE TO EXTRA SHIFT REQUIREMENTS, OUR COUNTY OFFALY BASED CLIENT IS
SEEKING A MACHINE SETTER FOR A **APPLY ON THE WEBSITE**-MONTH
FIXED-TERM CONTRACT TO COVER A VACANCY ON WEEKEND NIGHT SHIFT.
JOB TITLE MACHINE SETTER (WEEKEND DAY SHIFT 6.**APPLY ON THE WEBSITE**
PM - 6.**APPLY ON THE WEBSITE** AM
ROLE ACCOUNTABILITIES
This role will work across a number of areas, predominately cell 1,
with cover required for other areas when required.
KEY RESULT AREAS / KEY TASKS
* EHS
* Ensure compliance with and assist in the maintenance of a safe
company culture by working within relevant Company and Corporate
requirements and legislation governing environmental, health and
safety as principally contained in the Safety, Health and Welfare at
Work Act **Apply on the website**, Safety Cardinal Rules, Safety
Statement, etc. Report any equipment or process problems as
appropriate
* Ensure all machine safety guards are working.
* Highlight and work to eliminate unsafe methods/equipment/hazards
as appropriate.
* QUALITY
* Ensure quality in all aspects of work by following Standard
Operating Procedures (SOPs) and Standard Work Instructions (SWIs) and
maintaining compliance with all quality requirements.
* Set-up all machines as per relevant procedures.
* Ensure machines are set-up and run within validated parameters at
all times.
* Complete first-piece checks and all related paperwork. Ensure
product quality is to specification.
* Carry out on-line quality checks as per relevant procedures.
* Ensure equipment is set-up correctly 1st time to maximize quality
and minimize potential for defects.
* As the majority of work undertaken will take place in a clean-room
environment, GMP and 5S compliance is essential. Ensure equipment and
benches are cleaned after every set up and floors, storage areas, etc
are maintained to a high standard and take an active role in 5S
projects in your area
* MACHINERY
* Correct set-up, general maintenance and preventative maintenance
of production equipment.
* Ensure all equipment is set-up as per the relevant procedure and
parameter sheets.
* Troubleshoot mechanical problems and repair or replace parts as
appropriate.
* Ensure proper identification and storage of tools, gauges etc.
* Ensure equipment set-up is running within standard time and
produces **Apply on the website**% efficiency in order to achieve
associated OEE targets.
* Minimise downtime and work closely with Supervisors and
Engineering to ensure maximum utilization of equipment.
* Ensure set ups are completed in a timely manner and participate in
SMED projects, to continuously reduce set up times.
OTHER RESPONSIBILITIES WILL INCLUDE, BUT ARE NOT LIMITED TO, THE
FOLLOWING:
* Monitor scrap levels to ensure they do not exceed standard for any
operations and reduce defects off machines and thereby reduce scrap in
the plant.
* Identify process, equipment and documentation improvements where
possible and take part in improvement projects as assigned (e.g. Lean
Manufacturing/Six Sigma/SMED)
* Complete all identified training and development activities as
required including allocated MyLearning courses.
* Adhere strictly to company policies, procedures and plant key
behaviours as notified.
* Assist in the maintenance of a safe company culture by working
within the company**Apply on the website**;s environmental, health
and safety guidelines and Safety Cardinal Rules at all times. Report
any hazards, equipment or process issues in line with plant escalation
procedures
* Adhere to GMP based Quality Systems requirements for medical
devices and medicinal product (e.g. MDD, EU GMP Guidelines Vol IV Part
1 for medicinal product, ISO **Apply on the website**).
EXPERIENCE, QUALIFICATIONS AND SKILLS REQUIRED
* Education: Senior Trade / Recognised Mechanical / Plastics
qualification or Mechanical / Electrical Engineering Diploma
* Experience in an automated environment supporting high volume
mechanical / pneumatic manufacturing system is desirable
* Experience of automated equipment, PLCs, electro pneumatics,
servos, lubrication systems, preventative maintenance programmes.
* Experience in a high-volume manufacturing environment.
ESSENTIAL CRITERIA FOR THE POSITION ARE:
* Ability to articulate technical facts in a clear and concise manner
* Ability to work well in a team setting
* Self-starter, ability to use own initiative.
* Ability to take ownership for process, and drive troubleshooting
and improvement activities
* Ability to work under minimum supervision.
* Organised and resourceful with excellent attention to detail and
ability to get the job done
* Ability to multi-task and to work in a high paced environment with
an awareness of continued impact on production and the plant
performance.
* Ability to learn quickly and work on own initiative, under minimum
supervision
* Basic knowledge of mechanical, electrical and pneumatic components
* Quality awareness and a proven track record of excellent quality
standards
* Commitment to work within the ethos of the Medical Devices &
Supplies Guide to Compliance and Quality Manufacturing and the company
business conduct guidelines.
* Clear written and verbal communication skills
* Manufacturing process knowledge and experience
* Commitment to continuous improvements with the initiative and
ability to improve work processes
* An excellent standard of attendance and time keeping
* The ability to interact with employees at all levels of the
organisation and work as part of a team
Kelly Services are acting as an Employment Business in relation to
this role. Should you choose to apply, your information will be
processed in accordance with Kelly**Apply on the website**;s Privacy
Statement. For information regarding data protection at Kelly, please
visit the Kelly website and have a look into the Privacy Statement.
As an Equal Opportunities employer we welcome applications from all
suitably qualified persons regardless of their race, sex, disability,
religion/belief, sexual orientation or age.
We need : English (Good)
Type: Permanent
Payment:
Category: Others