field service engineer jobs

Near waterford
10Jobs Found

10 jobs found for field service engineer jobs Near waterford

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Facilities Engineer

Tandem Project Management

Waterford, Waterford
7 days ago
Waterford, Waterford
7 days ago

Summary:
My client is a bio pharmaceutical company who is looking for a Facilities Engineer to join their team in Waterford. The successful candidate will work as part of the Facilities team on capital projects on site.

Responsibilities:

  • Assist facilities engineer with capital projects both project management and execution.
  • Projects will include the migration of live commercial manufacturing and sampling suites to a QBMS.
  • Facility modifications to convert from soft gel manufacturing to accommodate commercial granulation suite.
  • Introduction of new facility equipment on site to serve sterile manufacturing facility.
  • Annual shutdown including HVAC and clean utility requalification to ISO.

Qualifications & Experience:

  • Degree in Engineering.
  • 5 years’ experience as a Facilities Engineer in a similar environment.
  • Pharmaceutical experience is essential.
  • HVAC, QBMS, compressed air and nitrogen plant equipment experience is strongly desired.
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Validation and Quality Engineer

Sigmar

Waterford, Waterford
19 days ago
Waterford, Waterford
19 days ago

Are you a Validation and Quality Engineer? Would you like to be part of an ever-growing team that understands the importance of on-time delivery and support to their customers while also providing high quality, reliable, and compliant products? Then this might be the role for you!!

Job Responsibilities

  • Create concise and accurate on-time technical reports.
  • Create and evaluate metrics to drive quality improvements.
  • Determine root cause of problems using CAPA/8D/A3 Problem Solving.
  • Lead and conduct internal audits.
  • Lead risk assessments (FMEA)
  • Develop validation documentation-plans protocols, procedures.
  • Track and resolve deviations.
  • Compile relevant documentation from suppliers for inclusion in validation protocols and reports.
  • Assist in the development of training material for qualification activities.

Job Role

  • Level 8 in the relevant field.
  • Experience in validation of manufacturing processes and clean room environment.
  • 5+ years’ experience in a Production environment
  • 5+ years’ experience in Quality department
  • 5 years Customer complaints management experience
  • GMP experience
  • ISO 9001-13485 CFR 820 knowledge

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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Manufacturing Engineer

Sigmar

Waterford, Waterford
24 days ago
Waterford, Waterford
24 days ago

Are you a Manufacturing Engineer with strong problem solving & validation skills? This could be the perfect role for you!

This company is a leader in medical devices spaces based in county Waterford!

Job responsibilities:

  • Designing manufacturing processes, procedures, and production layouts. 
  • Developing manufacturing processes and measurement systems.
  • Developing relevant work instructions and SOP’s and provides guidance to operations on training.
  • Providing guidance to operations regarding design concepts and specification requirements.
  • Ensuring processes and procedures are in compliance with regulations.
  • Delivering and managing projects within an agreed schedule.
  • Working with internal and external customers and partners to deliver on projects.
  • Utilizing LEAN, Six Sigma, and other best practice tools and principles for day-to-day problem solving and continuous improvement.
  • Writing and executing process and equipment validations (IQ/OQ/PQ).

 

Job Skills & Experience:

  • 3rd Level Engineering Degree with a good hands-on working knowledge of medical device assembly.
  • 4+ years of relevant experience in a highly regulated environment, 
  • Proven track record in the execution of protocols and validations to regulatory requirements.
  • Successful track record of project managing validation activities and cost reduction projects.
  • Technical knowledge of Automated Systems (Pneumatic, Electro-pneumatic, Robotic)
  • LEAN, Six Sigma experience
  • Monitoring of materials, equipment and process flows during validation and ramp-up related activities to ensure high levels of performance and OEE.
  • Process background (development, capability, optimization, validation) within a regulated industry.

For a confidential discussion on this or any other current job opportunity please contact Marcel Skolimowski on 021 4847 138 / marcel@sigmar.ie

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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Manufacturing Engineer

Sigmar

Waterford, Waterford
24 days ago
Waterford, Waterford
24 days ago

Are you a Manufacturing Engineer? Would you like to be part of an ever-growing team that understands the importance of on-time delivery and support to their customers while also providing high quality, reliable, and compliant products?

Job Responsibilities

  • Design manufacturing processes, procedures and production layouts.
  • Develop SOP’s and guide operations on training.
  • Ensure processes and procedures comply with relevant regulations.
  • Work with customers internally and externally as well as partners to deliver projects.
  • Utilize LEAN, Six Sigma and other best practices tools and principles daily.
  • Write and execute process and equipment validation (IQ/OQ/PQ).
  • Guide operations regarding design concepts and specification requirements.

Job Requirements

  • Level 8 in Mechanical, Biomedical or related Engineering/Science discipline.
  • Hands-on experience in Medical Device Assembly.
  • 4+ years of experience in a highly regulated environment.
  • Proven track record in the execution of protocols and validations.
  • Experience in managing validation activities and cost reduction projects.
  • Technical knowledge of Automated Systems (Pneumatic, Electro-pneumatic, Robotic)

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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Validation Engineer

BRIGHTWATER SELECTION (CORK) LIMITED

Waterford, Waterford
5 days ago
Waterford, Waterford
€35k - €45k Per Year
5 days ago
€35k - €45k Per Year

An expanding employer in the South has a vacancy for a Validation Engineer at their GMP facility. As part of a small dedicated team you'll work on a diverse range of products including equipment qualification, thermal mapping and CSV. For the right candidate a strong salary and benefits package is on offer for these roles which is on days.

About the Job:

  • Calibration, Installation, Operation & Performance qualification (IOPQ) of Laboratory equipment
  • Maintenance of schedules: Calibration, Qualification, Preventative Maintenance & re-qualification of equipment.
  • Execution of CSV (GAMP, RA, ERES Assessment) on lab Equipment.
  • Hosting & executing Installation, Operation & Performance qualification (IOPQ) of new equipment
  • Execution of temperature mapping on CTU (generating protocols, review, approval & execution).
  • Maintain the Validation Helpdesk generating reports & metrics and completing own assignments.
  • Calibration of equipment
  • Checking and signing off external certificates of calibration and generation internal certificates for same.
  • Ensure that all documentation is carried out on time, is accurate and legible and conforms to cGMP.
  • The execution of Temperature control mapping on CTU’s & ambient areas

About You:

  • Primary degree in Life Sciences or Engineering
  • At least 2-5 years’ experience in a laboratory or GMP regulated environment is desirable; preferably with Calibration/Validation experience.
  • Previous experience in GMP regulated environment.
  • Awareness of pharmaceutical processes for equipment calibration and validation.
  • Excellent technical writing, communication and organisational skills.
  • Quality oriented with the ability to consistently work to industry and client standards.
  • Experience with documenting analytical data and writing reports.
  • Passionate about quality and customer service.
  • Experience in IOPQ & understanding on GAMP for Lab equipment would be desirable

For more on the role call Nigel on 087 3618142 or send your CV for consideration.

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Manufacturing Engineer-2

Integer

New Ross
11 days ago
New Ross
11 days ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
JOB SUMMARY:
Provide engineering support to production through improved methods, processes, jigs and fixtures, tooling and machine enhancements to improve standard times and employee efficiencies in order to manufacture quality medical guide-wires at the target costs. Validate and introduce new equipment and processes to production. Create and maintain Device Master Record (DMR) Documentation through the order entry and ECO process. Train employees to perform processes as documented by standard operating procedures.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:
Employees are expected to support the quality concepts inherent in the business philosophies of Lake Region Medical including a variety of job related tasks, which may not be specific to this position profile.
Accountabilities include:
+ Learn Lake Region manufacturing processes and equipment in order to understand them, so as to be competent in providing technical support to production.
+ Lead or participate in projects, working closely with Production, Maintenance and Quality departments to implement the required changes to stabilise and improve processes. Goals include reducing defects, increasing efficiencies and increasing process uptime.
+ Employ Lean Manufacturing and Six Sigma methodologies such as process mapping, control charting, as appropriate in project work.
+ Monitor manufacturing activities, measure significant process characteristics and analyse variation in order to detect and reduce waste / scrap. Support the manufacturing process by taking corrective and preventative action on production delays and deviations.
+ Project management using standard Lake Region methodology.
+ Transfer of automation and new process projects to production, both within and between sites.
+ Transfer of New Products to production, both within and between sites.
+ Assist in training employees in new or improved processes.
+ Process and product validation.
+ Process / layout design and implementation.
+ Develop and support related documentation: - ECO generation to introduce changes and maintain DMR documentation.
+ Order Entry processing.
+ Sourcing, specifying and purchasing production equipment.
+ Jigs and fixture specification and development.
+ Assist in the specification of spare part lists.
+ Be an active member of the Lake Region Medical Limited team and work with all employees to develop a world class lean manufacturing system.
+ Comply with the Lake Region Medical Limited behavioural standards.
SKILLS AND KNOWLEDGE:
+ Ability to communicate and work with people inside and outside the Department as necessary to execute these responsibilities.Ability to train and lead assigned employees.
+ Ability to understand and follow appropriate Departmental policies, procedures, practices and to understand inter-relationships of people and functions.
+ Knowledge of manufacturing operations, systems and project management, including procurement, inventory control, quality control, production planning and control, test and inspection, layout.Knowledge of engineering theories, methods and work measurement techniques.
+ Ability to apply engineering methods in the definition, design, research, development, utilisation, maintenance, and cost-control of processes and equipment to build Lake Region products and improve qualities and reduce costs of such processes and products. MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS: College graduate with degree in Engineering, or equivalent experience. PHYSICAL DEMANDS: Work effectively with close tolerance. MENTAL DEMANDS:
+ Ability to work in an organised fashion.
+ Attention to detail.
+ Self-starter. WORKING CONDITIONS:
+ Day-shift operation, but may be required to change working hours or work other shift patterns occasionally as project responsibility dictates.
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
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Automation Engineer

BRIGHTWATER SELECTION (CORK) LIMITED

Waterford, Waterford
6 days ago
Waterford, Waterford
€55k - €65k Per Year
6 days ago
€55k - €65k Per Year

One of the South East's most attractive employers has a vacancy for an experienced Controls Engineer. Working in a dynamic and expanding site you will execute projects in a fast paced, multi-disciplined, cross-functional team environment. This role offers the opportunity to work on exciting new tech.

About the Job:

  • Manage production and the introduction of new technology through team leadership.
  • Provide technical and vision core competency support to Global Operations and Engineering on an as-needed basis, including possible off-hours, remote and onsite coverage rotation.
  • Provide Technical support and technical reference expertise to manufacturing and outside vendors in developing technical solutions for vision inspection technologies.
  • Project Management/ support of capital projects within the plant to drive increased volume and decreased cost across multiple manufacturing processes.
  • Provide Technical specification documents to external vendors for the purpose of trending and design/ build of new manufacturing equipment.
  • Support product, platform and cost improvement programs by delivering qualified vision systems. Interface with Engineering, SQA, QA and Operations to successfully validate software systems. Author and execute associated validation documents.
  • Provide technical and operations training on systems delivered.
  • Travel to vendor and other locations for on-site project support (domestic & international
  • Vendor management
  • Deliver projects on time and within budget
About You:
  • Electronics/ Electrical Engineering
  • Computer/Software development systems
  • PLC- Allen Bradley, Siemens
  • High Level language Programming e.g. C#, VB.net
  • Practical knowledge of machine vision systems including Cognex VPro and InSight desired
  • Methodical/Analytical approach to problem solving.
  • 3 - 5 years relevant experience
  • FDA regulated Medical Device
  • Project Management
  • PLC Software Development
  • Scada Software development
  • Manufacturing support
  • Development, documentation and approval of technical documentation

 

For more on the role call Nigel on 087 3618142 or send your CV for consideration.
C
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Validation Engineer

Crest Solutions

Waterford
19 days ago
Waterford
19 days ago

Crest Solutions have an open position for a Validation Engineer to join our team.


In the Validation Engineer role, you will be required to support capital projects/equipment qualification, new product introductions and the site requalification program. The Validation Engineer has a key role in ensuring the on-going validation and compliance of equipment, systems and processes. The following activities will be included as part of your role:


Responsibilities


       Designing, executing and reporting on validation studies for equipment, systems and processes.

       Ensuring validation studies are managed in conjunction with all required Sanofi standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.)

       Providing technical interpretation and guidance of current US FDA and EU validation requirements for solid dose manufacture, aseptic processing, lyophilisation, sterilisation and depyrogenation

       Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times

       Maintaining validation documentation through the validation lifecycle

       Participation in external regulatory inspections


Requirements & Qualifications

  • Relevant Engineering or Science qualification. Previous validation experience in sterile manufacturing, solid dose and devices would be highly advantageous for the role. 
  • 39 hour week with typical hours 8:00 to 16:30 (Mon-Thurs) and 8:00 to 15:30 (Fri) with occasional requirements to work outside these core hours and for business travel. The role reports to the Validation team leader.
  • You will have the opportunity to work in an energetic friendly team where team-work is essential. Due to the diverse of the site and the validation work, you will get exposure to many areas of the business with the chance to grow your career and develop your technical and professional skills. 

Why join Crest Solutions?


In Crest Solutions we understand that our people are our greatest asset. For this reason and many others, we take care of them. As part of the Crest Solutions team, you will be exposed to, and have the opportunity to work with, the latest cutting-edge technologies. The experience you gain in Crest Solutions will be multi-faceted.

This role also includes great personal benefits and professional growth opportunities. An example of what is offered to our team members is as follows:

        Competitive salary

        Full healthcare cover, leave benefits, life assurance, flexi-time and pension scheme

        A varied and exciting career with Crest Solutions with opportunities to work in a cutting-edge, innovative technological environment

        A structured approach to professional development opportunities with an educational assistance programme

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Senior Quality Engineer(Micro)

Integer

New Ross
30+ days ago
New Ross
30+ days ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
+ Adheres to Integer’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
+ Provide direction and training to other staff members performing duties in the microbiology area.
+ Develop, validate and maintain sterilization systems for Integer products. Conduct sterile validations and adoptions for new products. Coordinate and train staff to assure that all functions involved in completing the production sterile runs are carried out.
+ Develop and perform testing to ensure product safety and meet biocompatibility requirements of FDA, ISO, Japanese Ministry of Health and other regulatory agencies.
+ Develop and coordinate the cleanliness and contamination control programs for Integer manufacturing areas. Coordinate environmental monitoring on all cleanrooms. Provide training and guidance on regulations for cleanroom operations. Provide guidance on water quality management.
+ Select and audit contract sterilizer and testing laboratories.
+ Primary customer and regulatory body contact on sterilization, cleanliness policies and biocompatibility issues.
+ Complete protocols, final reports, and validations related to sterilization, biocompatibility and environmental monitoring.
+ Provide guidance and leadership to product development, production and product transfer teams on biocompatibility and sterilization requirements, as well as environmental impacts of new product introductions and production line layout changes.
+ Apply continuous improvement/lean concepts to identify and eliminate non-valued added tasks and/or activities.
+ Apply problem solving methodologies 8D, PDCA, DMAIC to identify root cause and create and implement corrective and preventive actions.
+ Performs other duties as required.
+ Knowledge & Skills:Special Skills:
+ Ability to apply advanced skills in microbiology and develop new methods to solve complex problems.
+ Ability to exercise independent judgement in developing methods, techniques and evaluation criteria
+ Skilled in multi-tasking and prioritizing.
+ Excellent written and verbal communication skills. Good presentation skills.
+ Specialized Knowledge:
+ General knowledge of GLP, GMP and QSR.
+ Working Knowledge of Medical Device Regulatory requirements including FDA, ISO and PMDA Ministry of Health (Japan).
+ Knowledge of scientific theories and methods pertaining to bioburden, LAL and water testing. Ability to interpret relation of bacterial identifications.
+ Knowledge of the methods of biocompatibility testing and the ability to interpret the data in relationship to current industry guidance.
+ Knowledge of EO sterilization process and requirements to validate and maintain a sterile cycle.
+ Other: Physical demands include equal amounts of sitting, standing and walking (including stairs and between buildings). High level of computer keyboard typing and computer screen viewing. Lift boxes up to 40 lbs. Use problem-solving techniques, high degree of attention to detail, work effectively on teams and communicate effectively with and lead people inside and outside the department.
+ Education & Experience:Minimum Education: Bachelor’s degree in one or more of the following disciplines: Biology (Biological Sciences), Microbiology, Molecular Cell Biology (MCB), Biochemistry or Chemistry. Alternatively two years of experience in a related field may be substituted for every year of education. Minimum Experience:
+ Five (5) to eight (8) years experience in the medical device manufacturing industry and at least (3) years’ experience in microbiology.
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
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Quality Engineer III

Integer

New Ross
30+ days ago
New Ross
30+ days ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
JOB SUMMARY
The Senior Quality Engineer will primarily be responsible for developing and maintaining all quality systems and monitoring production process for compliance to implemented process controls. Under minimal direction, manages Quality projects that may cover multiple sites. Duties will involve coordination, and scheduling of program or project activities. Assignments are broad in scope with the opportunity for the use of independent judgment. Essential Quality engineering skills are required.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
Employees are expected to support the quality concepts inherent in the business philosophies of Integer, including a variety of job-related tasks which may not be specific to this position profile.
POSITION REQUIREMENTS
Interfaces directly and regularly with customers (internal and external) staff. Often is included in critical business discussions with customers to bring deep insight to a problem or opportunity and establish a high level of credibility for Integer through demonstrated program management knowledge and expertise.
Proactively manage the risk associated with projects so that Integer’s and the customer’s business objectives are achieved. Minimize the uncertainties associated with projects relative to scope changes, customer expectations, business issues and other intangibles to enable successful completion of projects.
Involve and coordinate the input of all key functional groups and contributors to the proposed work plan.
Follows and develops Quality and Regulatory requirements including Integer’s policies, procedures, and appropriate regulatory requirements and have the standard Quality engineering skill set as outlined below.
Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Integer tools & templates were available.
As outlined above must have standard Quality engineering skills as outlined below:
1. Compliance with all Regulatory Standards, this includes:
Completion of internal audits to: ISO 13485 FDA QSR ISO 14000
b. Participation in Corporate auditing programs
c. Ensuring continued compliance with DMR
2. Develop and maintain a program ensuring only correctly validated equipment is used in production process. This will include:
Participation in validation protocol development Overseeing completion of validation or validation samples Supporting the engineering function to ensure compliance to related element of quality system
3. Liase with engineering departments on new product development projects to ensure;
All quality control requirements for non standard product are clearly understood All product samples for new product development qualification are inspected Relevant process controls are documented and transferred to production and suitably implemented with necessary training.
4. Monitor production process for compliance to implemented process controls to ensure quality product is shipped to customer and provide:
Trend analysis of data from the controls
Potential improvements for review with engineering based on the trends
Areas for Improvement to senior management
Review and propose changes to sampling plans based on trend analysis and changes to the system
5. Maintenance of customer concerns handling system in a timely manner including
Returned product analysis Organisation, filing and reporting of customer concerns
Ensure the requirements of the Electronic Documentation Management system
are understood and implemented at all levels of the organization.
Accountable to monitor manufacturing activities, measure significant process characteristics and analyse variation in order to detect and reduce waste
Ensure that in your absence, your area of responsibility is covered. Ensure that other departments are informed of your arrangements. Play a leadership role in encouraging the Company to achieve world class standards, above all by setting your own high professional standards as an example.
SKILLS AND KNOWLEDGE:
Ability to communicate and work with people inside and outside the department.
Excellent communicator: verbal, written and presentation skills.
Ability to train and lead assigned employees.
Ability to co-ordinate, plan and organise in a timely manner.
Knowledge of engineering theories and methods.
Rigorous attention to detail.
Ability to use Microsoft Office Suite (Excel, Project, Word, PowerPoint at a minimum) and ability to use / learn Oracle as the company ERP system (preferably Oracle)
MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS:
+ Demonstrate leadership in project management
+ Engineering, Science or Project Management Degree preferably with Quality Engineering included
+ Qualified systems lead auditor
+ Program Management certification or number of years experience
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
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Job Type

Contractor, Full Time

Posted

7 days ago

Description

Summary:
My client is a bio pharmaceutical company who is looking for a Facilities Engineer to join their team in Waterford. The successful candidate will work as part of the Facilities team on capital projects on site.

Responsibilities:

  • Assist facilities engineer with capital projects both project management and execution.
  • Projects will include the migration of live commercial manufacturing and sampling suites to a QBMS.
  • Facility modifications to convert from soft gel manufacturing to accommodate commercial granulation suite.
  • Introduction of new facility equipment on site to serve sterile manufacturing facility.
  • Annual shutdown including HVAC and clean utility requalification to ISO.

Qualifications & Experience:

  • Degree in Engineering.
  • 5 years’ experience as a Facilities Engineer in a similar environment.
  • Pharmaceutical experience is essential.
  • HVAC, QBMS, compressed air and nitrogen plant equipment experience is strongly desired.