Johnson & Johnson companies are equal opportunity employers.
SENIOR AUTOMATION ENGINEER-5678140305
Description
Janssen Supply Chain, a member of Johnson & Johnson's Family of Companies is currently recruiting for a Senior Automation Engineering position to be located in Vacaville, CA.
Janssen Supply Chain, a global organization responsible for supplying medicines to markets around the world. With Quality as their primary focus, this group strives to provides access and affordability through innovation and strong collaboration with their R&D and Commercial partners to deliver life changing solutions for patients in need.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The Senior Automation Engineer will have responsibility for providing Automation support to the site, implementing and maintaining automation control systems for processing equipment, and supporting projects to introduce additional automation to Vacaville. Initially, the role will consist of significant project work, but over time will transition to a support mode as the projects are completed in 2016/2017.
The Senior Automation Engineer will be the Subject Matter Expert for automation systems at the Vacaville site. This individual will support key IT/automation projects including OSI PI, Archestra System Platform and MES implementation. S/he will work closely with engineering and IT to ensure that new equipment is purchased and installed in line with Manufacturing Systems long term strategy. S/he will ensure alignment with platform and corporate groups (Manufacturing Systems, IT, etc.). This individual will work with manufacturing and engineering on continuous improvement projects related to controls systems. The Senior Automation Engineer will supervise contractors as necessary. S/he will drive project management of automation driven projects. Provide written and verbal communication such as status reports, progress reports and documentation to business partners and leadership. This individual will work with system integrators to ensure that appropriate support is available for the site.
The Senior Automation Engineer independently solves problems and resolves issues within area of expertise or escalates problems to the appropriate resource. S/he analyzes a chain of events and applies technical knowledge and collects facts and basic rationale to make recommendations for problem resolution. S/he applies compliance requirements within scope of responsibility, provides documentation as necessary, and participates in compliance activities as required.
The Senior Automation Engineer is the Subject Matter Expert for key projects, including OSI PI, Archestra and MES implementation. S/he will supervise contractors on automation related project work. S/he will work closely with local and corporate groups in the coordination of activities required for supporting systems implementation in a cGMP’s environment, including creating and maintaining SOPs and policies for the site around automation and key systems. S/he provides business representation and interaction with JSC Manufacturing Systems and IT discussion. This individual will provide IT/Automation SME and business process support for the site. S/he will interact with system integrators to ensure adequate system integrator support for the site.
Qualifications
A minimum of a Bachelor’s Degree is required. A degree related to Engineering or Computer Science or Business Administration with concentration in Information Systems is preferred. An advanced degree (i.e. Engineering, Automation, Business, IT or related field) is preferred. A minimum of 3-5 years of experience in the engineering or automation areas is required. The successful candidate should have experience working in a manufacturing environment. Strong experience with computers and Control Systems is required. The successful candidate has overall knowledge of cGMP’s and regulatory compliance, with experience in pharmaceuticals, or medical device, or related industry. Skills in project management, systems development, and implementation of automation projects in a pharmaceutical or medical device, or cGMP manufacturing environment is preferred. Experience with Invensys Automation systems, OSI PI historian and manufacturing execution systems (MES) is preferred. The position requires employee to be able to work with Wonderware SCADA, IFIX, RSView, Programming PLC, Honeywell EBI, OSI PI, PLCs, Controllers and the associated hardware. The position requires employees to be able to work with, infrastructure, Databases & Operating Systems technologies, the use of MS Office (Excel, Word, and PowerPoint) and Project Management. Experience with CFR Part 11 Compliance, system analysis, design, development, validation and implementation is preferred. The successful candidate must have excellent written and verbal communication and interpersonal skills. This position requires working regular shifts, occasionally requires working extended hours, and might be required to work on holidays and weekends. Occasional travel may be required. This position is located in Vacaville, CA and may require up to 10% travel.
BE VITAL in your career, Be seen for the talent you bring to work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI NA
Primary Location:North America-United States-California-Vacaville
Organization: Alza Corporation (6002)
Job Function: Technology Operations
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
SENIOR AUTOMATION ENGINEER-5678140305
Description
Janssen Supply Chain, a member of Johnson & Johnson's Family of Companies is currently recruiting for a Senior Automation Engineering position to be located in Vacaville, CA.
Janssen Supply Chain, a global organization responsible for supplying medicines to markets around the world. With Quality as their primary focus, this group strives to provides access and affordability through innovation and strong collaboration with their R&D and Commercial partners to deliver life changing solutions for patients in need.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The Senior Automation Engineer will have responsibility for providing Automation support to the site, implementing and maintaining automation control systems for processing equipment, and supporting projects to introduce additional automation to Vacaville. Initially, the role will consist of significant project work, but over time will transition to a support mode as the projects are completed in 2016/2017.
The Senior Automation Engineer will be the Subject Matter Expert for automation systems at the Vacaville site. This individual will support key IT/automation projects including OSI PI, Archestra System Platform and MES implementation. S/he will work closely with engineering and IT to ensure that new equipment is purchased and installed in line with Manufacturing Systems long term strategy. S/he will ensure alignment with platform and corporate groups (Manufacturing Systems, IT, etc.). This individual will work with manufacturing and engineering on continuous improvement projects related to controls systems. The Senior Automation Engineer will supervise contractors as necessary. S/he will drive project management of automation driven projects. Provide written and verbal communication such as status reports, progress reports and documentation to business partners and leadership. This individual will work with system integrators to ensure that appropriate support is available for the site.
The Senior Automation Engineer independently solves problems and resolves issues within area of expertise or escalates problems to the appropriate resource. S/he analyzes a chain of events and applies technical knowledge and collects facts and basic rationale to make recommendations for problem resolution. S/he applies compliance requirements within scope of responsibility, provides documentation as necessary, and participates in compliance activities as required.
The Senior Automation Engineer is the Subject Matter Expert for key projects, including OSI PI, Archestra and MES implementation. S/he will supervise contractors on automation related project work. S/he will work closely with local and corporate groups in the coordination of activities required for supporting systems implementation in a cGMP’s environment, including creating and maintaining SOPs and policies for the site around automation and key systems. S/he provides business representation and interaction with JSC Manufacturing Systems and IT discussion. This individual will provide IT/Automation SME and business process support for the site. S/he will interact with system integrators to ensure adequate system integrator support for the site.
Qualifications
A minimum of a Bachelor’s Degree is required. A degree related to Engineering or Computer Science or Business Administration with concentration in Information Systems is preferred. An advanced degree (i.e. Engineering, Automation, Business, IT or related field) is preferred. A minimum of 3-5 years of experience in the engineering or automation areas is required. The successful candidate should have experience working in a manufacturing environment. Strong experience with computers and Control Systems is required. The successful candidate has overall knowledge of cGMP’s and regulatory compliance, with experience in pharmaceuticals, or medical device, or related industry. Skills in project management, systems development, and implementation of automation projects in a pharmaceutical or medical device, or cGMP manufacturing environment is preferred. Experience with Invensys Automation systems, OSI PI historian and manufacturing execution systems (MES) is preferred. The position requires employee to be able to work with Wonderware SCADA, IFIX, RSView, Programming PLC, Honeywell EBI, OSI PI, PLCs, Controllers and the associated hardware. The position requires employees to be able to work with, infrastructure, Databases & Operating Systems technologies, the use of MS Office (Excel, Word, and PowerPoint) and Project Management. Experience with CFR Part 11 Compliance, system analysis, design, development, validation and implementation is preferred. The successful candidate must have excellent written and verbal communication and interpersonal skills. This position requires working regular shifts, occasionally requires working extended hours, and might be required to work on holidays and weekends. Occasional travel may be required. This position is located in Vacaville, CA and may require up to 10% travel.
BE VITAL in your career, Be seen for the talent you bring to work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI NA
Primary Location:North America-United States-California-Vacaville
Organization: Alza Corporation (6002)
Job Function: Technology Operations
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement