Position

QUALIFICATIONS

Embedded Engr II

The purpose of Embedded Engr II role is to ensure robust product quality in collaboration with Honeywell technology and business stakeholders. The role demonstrates technical leadership across multiple product subsystems and takes ownership for technical capability development and mentoring in team.

Education

B.E. (Bachelor of Engineering) and B.Tech. (Bachelor of Technology) – Instrumentation and Control, Electrical, Electronics or Equivalent.

Experience

Extensive experience (5-10 Years) in Batch, Life Sciences, Pharmaceutical domain / verticals and strong experience in Manufacturing Execution System (MES) and Distributed Control Systems (DCS).

Desired Skills

Hands on/In depth understanding of Distributed Control Systems for Batch, Life Sciences and Pharma Industries.
Domain understanding of DCS system deployment in Pharma, Batch or F&B verticals, having working experience of Manufacturing Execution System (MES) and Control Systems for Batch process.
Candidate is required to have Strong Domain Knowledge on Pharma/Drug Manufacturing Sector, the Compliance/Regulatory requirements of the Pharma Sector.
Candidate should have a strong understanding of ISA S88, ISA S95, FDA, GMP and cGMP Standards and guidelines.
It will be preferred if the Candidate also has a strong process and Operations knowledge/Experience in Batch Processing Industries like Pharma, Spec Chem, Food & Beverages
Hands-on work experience with top Life Sciences, Pharma, Biopharma, CDMO, API, Nutraceuticals, Cosmeceuticals, Food Processing, Cell & Gene Therapy manufacturing companies.
The Candidate should have experience in Project Engineering, Commissioning and Maintenance of Pharma/Batch Projects with some of following systems e.g. Honeywell Experion Batch Manager, Total Plant Batch, etc.
The Candidate should have experience in Engineering, Operation and Maintenance of Pharma/Batch MES Manufacturing Execution System platforms and modules like MBR, EBR, W&D, Elogs and interfaces to L3/L4 Systems like ERP, QMS, DMS, TMS, LIMS, etc
Working experience deploying or operating MES at Pharma companies.
Should have had experience in Batch Design – Process and Equipment Model based on the Process and Design Inputs. He/She must have experience of FAT/SAT of Batch Projects.
Good knowledge on cGMP documentation.
Knowledge on Digital platform SAP & TrackWise to handle PM/BD and QMS documents.
Should have working knowledge on Batch sequence programming using ladder programming, FBD, SFC and other languages described in IEC61131-3 standard.
Should have sound knowledge of different communication protocols for third party interfaces and for field device integration.
SDLC process and various Test management tools and Processes.
Virtualization concepts and deployment understanding.
Proven track record of managing complex programs successfully which have critical business knowledge and skills
Candidate should be able to support, lead and influence team to drive changes successfully
Understanding of various testing and development methodologies, Test Automation using Selenium, Python, JMeter, Test Complete, etc and DOE (Design of Experiments) techniques to optimize efforts
Strong communication and Interpersonal skills and should have worked extensively with global stakeholders like projects, TAC, services etc
Hands on knowledge on breadth of product including various communications standards, controllers, interfaces, Knowledge of Honeywell systems, various performance and capacity specifications etc.
Continuous improvement and Innovative mindset is essential and candidate should have created/implemented new ideas

Primary Responsibilities:-

Uses strong domain and product knowledge to ensure completeness of deployment scenarios, use cases and user profile and built-in product quality.
Responsible for the product quality and defining test topology for assigned product lines including large systems.
Responsible for creating test procedures as for Honeywell Life Sciences Products and Solutions catering to the requirements of the Pharma Industry and Compliance regulations and should ensure full coverage.
Responsible for developing Test Strategies/Scenarios and sequences typically applied in Pharma Manufacturing to emulate Scenarios close to Drug Manufacturing Practices
Responsible for the System level Test Coverage and reduction in Post Release defects to the Customer/End User
Responsible for review of Architecture and design and can design test strategies to cover non-functional requirements in the program.
Using test environment that almost replicate customer sites and develop better customer scenarios for validation.
Candidate will need to ensure test procedures are automated & simulations defined wherever applicable that should have in depth test coverage as well as reduce cycle time.
Responsible for interacting with key Stakeholders such as Architects, Program Management, Development Leads and Test System Engineer
Should be able to support/resolve queries from Project Engineering teams and TAC
Should be able to drive improvements in Test methodologies inline with the best in class Standards
Will have to closely collaborate and work with product development team. Requires to understand the product requirements, plan the testing, prepare test cases, execute the testing and report the defects in defect tracking tool.
Ensuring timely completion and submission of weekly test reports.

About Us

Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments – powered by our Honeywell Forge software – that help make the world smarter, safer and more sustainable.