Celgene

Manager, Automation Engineer, P&O, Control Systems, SYR Digital Plant

Posted on: 6 Apr 2021

Syracuse, NY

Job Description

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

The Automation Engineer is a key member of the Digital Plant team supporting process controlled automated systems at the Syracuse, NY manufacturing facility. The primary role of the automation engineer is to design and lead implementation of engineering solutions for process equipment controls, S88 batch controls, hardware, device integration, and server support for the production and building control systems. Position requirements are listed below.

Duties/Responsibilities:

* Owns end-to-end responsibility for managing automation related projects, ensuring processes are configured per user functional requirements.
* Influences vendor roadmaps to align with BMS strategy.
* Support the operation of all GMP/ Non GMP manufacturing systems (Process Automation Systems and Building Automation Systems) in the Manufacturing facilities at Syracuse, NY.
* Investigate the root cause of Digital Plant problems and propose solution to prevent recurrence.
* Act as an Automation SME on deviation investigation teams to support manufacturing operations and designs technical solutions to satisfy manufacturing requirements.
* Support the configuration, testing and implementation of process control solutions to a variety of complex technical problems.
* Ensure the documentation of the knowledge base on how to resolve issues encountered, thus facilitate the job for future activities.
* Provide oversight and ownership on the Automated Manufacturing processes, including Batch Recipes, Formulas, Phases, automated sequences, hardware and networking components.
* Act as the project lead for Lean OpEx initiatives that align with site strategy and interact with cross-functional groups to achieve departmental and organizational goals.
* Conduct all job activities in accordance with cGMP and EHS requirements.
* Provide training of automated solutions with operations staff to ensure understanding how the automated software programs functions as well as automation colleagues for support.

Specific Knowledge, Skills, Abilities, etc:

* Knowledge of products and technologies provided by major automation vendors, including: DeltaV, Allen Bradley, and GE.
* Experience in deploying computing hardware and communication systems that include PCs, servers, thin clients, Ethernet infrastructure. Knowledge of instrumentation busses (Foundation FieldBus, ProfiBus, DeviceNet, etc.) a plus.
* Ability to develop and execute innovative process control solutions for continuous improvement for control of the manufacturing operations.
* Understanding of Process Flow Diagrams, Standard Operating Procedures, and Manufacturing Batch Records to design appropriate controls system programming.
* Technical problem solving and analysis skills as well as good communications skills (verbal and written).
* Demonstrated experience in process control methods and industry standards.
* Demonstrated ability to create and understand process design documents such as P&IDs, electrical schematics, and loop drawings.
* Demonstrated ability to effectively lead or participate in multi-disciplined team environment to achieve goals.
* Knowledge and understanding of applicable regulatory requirements.
* Adaptable to a fast paced, complex and ever-changing business environment.

Education/Experience/ Licenses/Certifications:

* Advanced knowledge of engineering or sciences generally attained through studies resulting in a B.S. in, engineering, science, biochemistry or related discipline or its equivalent is highly desired.
* Direct biologic manufacturing experience of 5+ years.
* Significant knowledge and proven expertise of engineering and operating principles related to typical biopharmaceutical upstream and downstream processing and support equipment including but not limited to bioreactors, filtration and ultra filtration, CIP, SIP, centrifugation, chromatography, and media and buffer make-up.
* Experienced with current industry standards for Safety and Automation and with current government regulations regarding biotech-producing facilities.
* Experience with Emerson DeltaV Distributed Control Systems and Rockwell/Allen Bradley PLCs preferred.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Celgene

Summit, NJ

Celgene Corporation, a biopharmaceutical company, discovers, develops, and commercializes therapies for the treatment of cancer and inflammatory diseases worldwide. It offers REVLIMID, an oral immunomodulatory drug for multiple myeloma (MM), myelodysplastic syndromes (MDS), and mantle cell lymphoma; POMALYST/IMNOVID to treat multiple myeloma; OTEZLA, a small-molecule inhibitor of phosphodiesterase 4 for psoriatic arthritis and psoriasis; and ABRAXANE to treat breast, non-small cell lung, pancreatic, and gastric cancers.

The company’s products also include IDHIFA for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (rrAML) with an isocitrate dehydrogenase-2 mutation; VIDAZA, a pyrimidine nucleoside analog for intermediate-2 and high-risk MDS, chronic myelomonocytic leukemia, and AML; THALOMID to treat patients with MM; and ISTODAX, an epigenetic modifier. Its preclinical and clinical-stage product candidates include small molecules, biologics, and cell therapies for immune-inflammatory diseases, myeloid diseases, epigenetics, protein homeostasis, and immuno-oncology.

The company has agreements with BeiGene, Ltd; Acceleron Pharma, Inc.; Agios Pharmaceuticals, Inc.; bluebird bio, Inc.; Lycera Corp.; Juno Therapeutics, Inc.; EXSCIENTIA LTD.; and IMIDomics SL, as well as immuno-oncology collaboration with Sutro Biopharma. Celgene Corporation was founded in 1980 and is headquartered in Summit, New Jersey.