Sr. Engineer II, Site Automation
About The Position
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. BeOne Medicines US Manufacturing Co., Inc. seeks Sr. Engineer II, Site Automation in Hopewell, NJ. Job Duties: Support projects in the design, development, and qualification of automated processes, equipment, and systems; including managing the work of contract automation resources. Author, develop and review technical documentation such as Functional Design Specifications, Hardware Design Specifications, Software Design Specifications, Control Panel Layout and circuit drawings, operations and maintenance manuals, instrumentation specifications and As-Built documentation. Utilize hands-on experience with program administration, configuration and modification of DCS, PLC, BAS, MES, Historian and HMI/ SCADA software applications including Rockwell PlantPAX, Siemens TIA portal, WIN911 and Aveva. Maintain per GxP requirements. Directly support 24x7 operations with troubleshooting and issue resolution with respect to computer and automation systems. Work on small cross functional teams in support of small projects or initiatives. Author SOPs on automation systems for the site. Requires working in an industrial manufacturing environment including GMP gowning.
Requirements
- Master’s degree (or its foreign degree equivalent) in Biotechnology, Engineering (any field), or a related quantitative discipline, and 4 years of experience in the job offered or in any occupation in related field, OR Bachelor’s degree (or its foreign degree equivalent) in Biotechnology, Engineering (any field), or a related quantitative discipline, and 6 years of progressively responsible experience in the job offered or in any occupation in related field.
- Project Management
- Working in regulated environments (OSHA, EPA)
- Authoring technical manuals
- Authoring and reviewing Standard Operating Procedures specifically for a manufacturing environment
- Instrument calibration
- Any suitable combination of education, training and/or experience is acceptable.
Responsibilities
- Support projects in the design, development, and qualification of automated processes, equipment, and systems; including managing the work of contract automation resources.
- Author, develop and review technical documentation such as Functional Design Specifications, Hardware Design Specifications, Software Design Specifications, Control Panel Layout and circuit drawings, operations and maintenance manuals, instrumentation specifications and As-Built documentation.
- Utilize hands-on experience with program administration, configuration and modification of DCS, PLC, BAS, MES, Historian and HMI/ SCADA software applications including Rockwell PlantPAX, Siemens TIA portal, WIN911 and Aveva.
- Maintain per GxP requirements.
- Directly support 24x7 operations with troubleshooting and issue resolution with respect to computer and automation systems.
- Work on small cross functional teams in support of small projects or initiatives.
- Author SOPs on automation systems for the site.
- Requires working in an industrial manufacturing environment including GMP gowning.
Benefits
- Medical
- Dental
- Vision
- 401(k)
- FSA/HSA
- Life Insurance
- Paid Time Off
- Wellness
- opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
