Process Engineer - Blackpool-00000C35
Description
DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world, built upon the strong legacies of two great companies. We are a total solutions company. DePuy Synthes Companies offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high quality offerings help advance the health and wellbeing of people around the world.
The unmet needs in orthopaedic and neurological care are significant. With insights from patients, physicians, providers, payors and policymakers to guide us, DePuy Synthes Companies are uniquely positioned to meet these needs and deliver life-changing medical innovation. At DePuy Synthes Companies, we aspire to be your partner of choice, delivering high standards of quality in everything we do.
Duties & Responsibilities (leadership, people development, planning and execution)
- Process review and optimisation of specified process area/s.
- To input into new product development, to ensure timely introduction into production and that they are operationally cost effective.
- Initiation / completion of deviations, remedial actions, CAPA's and other quality system documentation.
- Control and direct manufacturing validation effort for existing and new processes.
- Active member of multifunctional process and production improvement team.
- Application of world class manufacturing tools and techniques (Lean, ME2) within aligned process areas.
- Problem identification and resolution to root cause.
- Responsible for Waste reduction in area
- Actively drives process improvement projects to achieve OEE targets for area of responsibility
- Leadership and coordination of onsite Process Excellence initiatives and activities including certification, re-certification and promotion of PE awareness on site.
- Input into machinery purchases, including user requirement specification, investigating new technologies for existing processes.
- To follow and promote Company, HS&E and Quality standards to enable the site to achieve and maintain excellent results
- To liaise with outside contractors whilst leading projects from conception to commissioning and handover.
- To ensure that processes are robust and as efficient and effective as possible.
Quality and Compliance Related Responsibilities
- Ensures that all activities are carried out in compliance with all regulations and laws governing business and quality operations (FDA / GMP / BSI / ISO, etc.).
- Responsible for ensuring company compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Accountable for HSE compliance for their area of responsibility.
Qualifications
Experience
Minimum 2 years experience in engineering / process engineering preferably in a medical devices / pharmaceutical environment. Proven track record of installing / validating new equipment and processes in a highly regulated environment. Experience in Lean Manufacturing Initiatives to deliver business benefit. Ability to deliver projects on time and to budget. Able to demonstrate process, equipment improvements and waste reduction savings
We respectively request Government Officials to identify themselves as such on application; for the purpose of the Foreign Corrupt Practices Act. If you decide to apply for the position, any personal data which you provide shall be processed by Johnson & Johnson Medical, a Johnson & Johnson company. Your personal data shall be processed for the purposes of recruitment, recruitment policy and selection.
Primary Location:Europe/Middle East/Africa-United Kingdom-England-Blackpool
Organization: DePuy Synthes, Inc. (6033)
Job Function: Process Engineering
Description
DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world, built upon the strong legacies of two great companies. We are a total solutions company. DePuy Synthes Companies offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high quality offerings help advance the health and wellbeing of people around the world.
The unmet needs in orthopaedic and neurological care are significant. With insights from patients, physicians, providers, payors and policymakers to guide us, DePuy Synthes Companies are uniquely positioned to meet these needs and deliver life-changing medical innovation. At DePuy Synthes Companies, we aspire to be your partner of choice, delivering high standards of quality in everything we do.
Duties & Responsibilities (leadership, people development, planning and execution)
- Process review and optimisation of specified process area/s.
- To input into new product development, to ensure timely introduction into production and that they are operationally cost effective.
- Initiation / completion of deviations, remedial actions, CAPA's and other quality system documentation.
- Control and direct manufacturing validation effort for existing and new processes.
- Active member of multifunctional process and production improvement team.
- Application of world class manufacturing tools and techniques (Lean, ME2) within aligned process areas.
- Problem identification and resolution to root cause.
- Responsible for Waste reduction in area
- Actively drives process improvement projects to achieve OEE targets for area of responsibility
- Leadership and coordination of onsite Process Excellence initiatives and activities including certification, re-certification and promotion of PE awareness on site.
- Input into machinery purchases, including user requirement specification, investigating new technologies for existing processes.
- To follow and promote Company, HS&E and Quality standards to enable the site to achieve and maintain excellent results
- To liaise with outside contractors whilst leading projects from conception to commissioning and handover.
- To ensure that processes are robust and as efficient and effective as possible.
Quality and Compliance Related Responsibilities
- Ensures that all activities are carried out in compliance with all regulations and laws governing business and quality operations (FDA / GMP / BSI / ISO, etc.).
- Responsible for ensuring company compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Accountable for HSE compliance for their area of responsibility.
Qualifications
Experience
Minimum 2 years experience in engineering / process engineering preferably in a medical devices / pharmaceutical environment. Proven track record of installing / validating new equipment and processes in a highly regulated environment. Experience in Lean Manufacturing Initiatives to deliver business benefit. Ability to deliver projects on time and to budget. Able to demonstrate process, equipment improvements and waste reduction savings
We respectively request Government Officials to identify themselves as such on application; for the purpose of the Foreign Corrupt Practices Act. If you decide to apply for the position, any personal data which you provide shall be processed by Johnson & Johnson Medical, a Johnson & Johnson company. Your personal data shall be processed for the purposes of recruitment, recruitment policy and selection.
Primary Location:Europe/Middle East/Africa-United Kingdom-England-Blackpool
Organization: DePuy Synthes, Inc. (6033)
Job Function: Process Engineering