What are the responsibilities and job description for the DeltaV Automation Engineer position at NNE?
We are looking for a DeltaV Automation Professional to join our team of experts in pharma automation and IT. As a team, we are working on shaping the future of sustainable and intelligent pharma facilities. Why do we need you? We expect you to analyze, design, develop, implement, and maintain DeltaV automation hardware, software, and process solutions. Your role will be key in ensuring that automation processes are efficient and compliant with industry standards.
Primary Duties and Responsibilities:
How You Might Spend Your Days:
Required Qualifications:
To apply for the position there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:
Deadline of application is 5/30/2025
We will invite to interviews on a running basis.
Primary Duties and Responsibilities:
How You Might Spend Your Days:
- You'll be working with a motivated, multi-functional team where you’ll be responsible for deliverables where output is Complex.
- Leading project team – Setting direction, planning, execution & handover.
- Manage automation projects for on-time delivery and within budget.
- Supervising / Development of functional specifications of Complex Units.
- Supervising / Developing DCS Application coding based on programming standards and design guidelines, performing reviews to ensure consistency.
- Co-ordination and alignment with cross-functional teams i.e. Process/Mech. & E/I Team
- Troubleshoot, analyze, and resolve control system issues.
- Testing and Verification to ensure that programming or coding is meeting functionality.
- Commissioning and Qualification to ensure that systems and equipment meet the requirements of end-users and regulatory agencies with multi-discipline collaboration.
- Sharing lessons learnt and contribute to continuous improvement.
- Review work and ensure coaching and training of more junior colleagues in your discipline.
- Making decisions that impact own team and possibly other teams or operational areas.
- Develop, review, and/or execute automation qualification and validation protocols.
- Demonstrate subject matter expertise and handle complex challenges.
- Build customer relations within your field of expertise by delivering excellent services.
- Able to perform work independently, handle complex challenges and apply specialist knowledge when adapting solutions.
- Able to identify better practice and improve procedures, processes, tools, equipment, or techniques based on industry specific knowledge & business experience.
- Able to take initiative, prioritize, and plan for own work and/or team to reach deadlines.
- Able to make decisions under conditions of uncertainty, proactive in identifying roadblocks.
- Able to drive team towards milestone achievements.
- Able to Challenge solutions and Stakeholders whenever required to align with Standards.
- Enjoy sharing knowledge to help build up others' competences.
- Having a positive approach and can be persistent when facing challenges.
- Have the ability to collaborate across all levels of the organization both internally and externally.
- Ensure project compliance in accordance with NNE’s quality management system, standards, and methods as a basis for execution.
Required Qualifications:
To apply for the position there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:
- B.S. or M.S. in Chemical, Electrical, Computer Science, Bio-Process Engineering, or related field.
- 8 years’ experience designing, implementing, and supporting manufacturing automation solutions.
- 6 years of strong Emerson DeltaV Batch experience required with knowledge of DeltaV hardware.
- Good knowledge of GAMP lifecycle.
- Knowledge of PCSD library would be an added advantage.
- Good understanding of Process Automation System Architecture, ISA S88 Batch & good engineering practice.
- Good knowledge on pharma life cycle /processes, GAMP, 21CFR, GDP & regulatory knowledge would be preferable.
- Strong Design/ functional specifications (Control Module, EM and Phase class) experience & application development for recipes would be preferable.
- Experience in project management, including coordinating teams, budgets, and timelines.
- FAT, SAT, IQ and OQ experience would be required.
- Strong leadership, communication, and collaboration skills.
- Collaboration and innovation-based culture.
- Competitive pay and annual performance bonus for all positions.
- Generous paid time off including 14 paid holidays (3 Floating).
- Health Insurance, Dental Insurance, Vision Insurance – effective day one.
- Guaranteed 8% 401K company contribution.
- Family Focused Benefits include 14 weeks paid parental & 6 weeks paid family medical leave.
- Free access to Novo Nordisk-marketed pharmaceutical products.
- Tuition Assistance.
- Life & Disability Insurance.
- Employee Referral Awards.
Deadline of application is 5/30/2025
We will invite to interviews on a running basis.