Senior Software Engineer - Syncade Developer

Posted:
11/13/2024, 4:00:00 PM

Location(s):
Telangana, India ⋅ Hyderabad, Telangana, India

Experience Level(s):
Senior

Field(s):
Software Engineering

Workplace Type:
Hybrid

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.

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. Read more: careers.bms.com/working-with-us.

BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.

Senior Software Engineer – Syncade Developer

Summary:

The role is responsible for development, maintenance and support of the global Enterprise Manufacturing Execution Systems (EMES) solution that is utilized globally.

Scope:

EMES core platform (Emerson Syncade), components, interfaces, custom tools, and any customizations that support digital manufacturing systems and operations including.

Master data management (items, users rights, equipment’s, locations, Workorder…) Master batch record edition & approval (including workflows) Master batch record review & approval (by Exception) Guidance / instructions Production execution Weighing & Dispensing Communication to equipment or Scada systems Equipment management Material flow management Traceability / Genealogy Labelling Reporting Articulation with ERP, quality, logistic & shopfloor systems (LIMS, Documentation, Deviation management, Serialization, OEE,…)

Key Responsibilities:

Deliver innovative "state of the art" tools enabling performance for manufacturing processes across the industrial affair sites. Allow new generation of deployment – more Agile & business centric. Maintain robust and highly available solutions to operate industrial processes efficiently. Engage with the BU business stakeholders, Development Team, Program team, users, and partners to understand requirements, deliver solutions, enhancements, Bug Fixes and resolution of issues. Share the responsibility for design custom objects and support of business solutions based on site’s needs for MES processes and functions. Work closely with MES Product Owner to create and maintain a product backlog according to defined business value and/or ROI targets. Manages the risk and ensures prompt resolution of issues, removing roadblocks and impediments. Proactively manages communications within team and about project status and next steps. Work with Domain Architects (including Data, Infrastructure, Application and Security architects) to ensure that Functional Solution Design aligns with system design guidelines and enterprise architecture standards. Work with Infrastructure, Security (DMZ for Plant and DMS for Office network separation), Various Protocols etc. Create and maintain Functional user manuals, Functional documentation, other project collaterals et cetera. Understand other tools related to MES system, Interface with related Edge applications, RFID, Scanner, Robots, Pick Systems, et cetera.

Experience & Knowledge:

 

  • 5+ years’ work experience in Manufacturing Execution System(MES) domain in Pharma industry
  • Demonstrated experience in a multicultural/multilanguage environment and in a matrixial organization.
  • Knowledge of Manufacturing Processes in industrial plants within pharmaceutical context (GXP regulations)
     

Core Skills:

  • Manufacturing Execution System Business Processes including Master Batch Record and Review by Exception.
  • Strong Knowledge of Pharma Execution and or Emerson Syncade Product
  • Strong Expertise in development languages: VB, VBScript, ASP.NET, C#, Java.
  • Strong Expertise in web development of preferably secure, scalable web applications in JavaScript /JQuery.
  • Experience in server-side coding using NodeJS, ExpressJS,ASP,C#,Java.
  • Experience in client-side coding using HTML5, CSS, XML,JavaScript, ReactJS,Angular,JQuery. (all optional)
  • Experience with AJAX, XML, JSON, and useful Design Patterns
  • Extensive knowledge of REST/ GraphQL API client & server. Experience building API-driven applications or endpoints.
  • Knowledge on Rest API, SOAP framework, XML, Web service design would be a nice to have.
  • Strong Knowledge of Digital technologies as AWS or AZURE cloud, containers, micro services, dev-ops, …
  • Experience in T-SQL programming language, including database design and optimization.
  • Strong Expertise of Infrastructure technologies & services as network, Windows System administration, SQL, MVC.
  • Expertise with web architecture, cross-platform integration, and building scalable applications in heterogeneous environments.
  • Extensive knowledge and experience with Test-Driven Development and/or Behavior-Driven Development.
  • Working Knowledge of the full SDLC.
  • Strong Expertise in Reporting tools : Infobatch.
  • Strong communication and interaction skills
  • Customer Driven
  • Applying standard in an Agile matter
  • Ability to challenge, open minded and active listening.
  • Knowledge of Pharma industry regulatory best practices applied to Digital development and software validation.
  • Ability to work across global sites and cultures.
  • Optional travel up to 5% domestically and internationally

Qualifications - required education, experience & skills:

  • Bachelor’s degree in engineering, master’s in computer applications (MCA)
  • 6-10+ years of solid work experience and having worked as technical lead in designing, building, deploying and supporting automation and execution systems.
  • At least 2 IT full-life cycle implementations acting in key Functional roles such IT project lead, cut-over lead, migration lead, etc.
  • Strong domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems.

#HYDIT #LI-Hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

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.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Website: https://bms.com/

Headquarter Location: New York, New York, United States

Employee Count: 10001+

Year Founded: 1887

IPO Status: Public

Last Funding Type: Post-IPO Debt

Industries: Biotechnology ⋅ Health Care ⋅ Medical ⋅ Pharmaceutical ⋅ Precision Medicine