Senior Engineer I, Automation
3 weeks ago
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Position Summary
The Senior Automation Engineer I will be responsible for controls systems design, programming, simulation and testing, validation, troubleshooting, and project documentation. Equipment planned for automation control includes bioreactors and media processing system. Position will include participating in initial qualification activities (CSV, recipe qualification) and ongoing activities such as recipe revision, periodic review, validation, and integration with other GxP electronic systems. This position will also provide automation support to Bothell Manufacturing Operations as well as work with global teams to design automated solutions that improve processes and integrate new equipment. The Senior Automation Engineer I role will represent site automation in cross functional efforts and work collaboratively with system owners and quality groups.
Key Responsibilities Serve as automation engineer in Emerson DeltaV platform for both established recipes and introduction of newly automated equipment.
Design automation strategies in Emerson DeltaV by defining class-based modules, using sequence flow charts, phase logic modules, and creating process operator graphics.
Collaborate with internal and global functions (Process Development, Computer System Validation, Quality) to translate requirements into automated solutions.
Adhere to software development lifecycle (SDLC) practices and S88 automation standards.
Author, review, and perform recipe validation.
Maintain qualification/validation documentation (protocols, reports, schedule).
Partner with key stakeholders to define system requirements and identify risk.
Meet control strategies based on functional specifications, existing code, and operator input.
Provide automation impact assessments for process and material changes.
Provide installation and start up support for projects as needed. Start up support includes but not limited to installation consulting, loop check support, startup assistance, loop tuning, and configuration modifications.
Represent automation programs during regulatory inspections.
With IT, deliver integrated solutions across multiple platforms including DeltaV, Emerson Syncade, Informetric InfoBatch, data historian, and benchtop equipment.
Implement and maintain risk assessments that ensure process controls address known risks.
Provide training for system use, troubleshooting, and recipe maintenance to manufacturing and other groups.
Interact with end users, IT, maintenance, and support groups while troubleshooting issues.
Request quotes from vendors for approved equipment, software, and services.
Identify and implement continuous improvement, efficiency, and system reliability projects.
Qualifications & Experience
Specific Knowledge, Skills, Abilities: 4+ years relevant biopharmaceutical industry experience.
4+ years of automation/process control system experience is strongly preferred.
Experience with Emerson DeltaV batch processing preferred.
Experience with InfoBatch Electronic Reporting system preferred.
Experience with Aveva PI Data Historian system preferred.
Experience with cGMP/GMP, ICH guidelines, data integrity, computer system validation, safety principles, and working within a regulated industry.
Education/Experience/ Licenses/Certifications:
BS in engineering, computer science, biology, or equivalent scientific discipline.
The starting compensation for this job is a range from $92,000 to $121,000, plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers Site.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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