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Advanced Manufacturing Tech Solutions (AMTSOL)AA

PTO (DeltaV) - Software Lead Engineer

AMTSOL delivers technology solutions for life science manufacturing, specializing in GMP manufacturing systems, automation, MES, and digital transformation for pharmaceutical and biotech companies.

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About us : At AMTSOL, we deliver innovation through technology for Life Sciences Manufacturing, driving Pharma 4.0 and Digitalization to help regulated manufacturers accelerate speed to market, ensure GxP compliance, and enhance operational efficiency. With a strong presence across Singapore, Europe, India, and the USA, we specialize in end-to-end implementation and support of GMP manufacturing systems and solutions, spanning Automation, Manufacturing Execution Systems (MES), IT/OT Networking, and Digital Technologies.

Overview: The Program Technical Office (PTO) is responsible for defining and maintaining the automation philosophy, technical standards, and ensuring consistency across all automation projects. During project execution, the PTO provides guidance and oversight to individual project teams, ensuring alignment with the overall automation strategy and compliance with regulatory and technical standards.

Key Responsibilities:

  • Provide technical oversight for assigned automation projects.
  • Work closely with project technical teams to ensure alignment with program-wide automation philosophy and standards.
  • Collaborate with Digital/MES workstream leads to integrate automation and digital solutions seamlessly.
  • Support project teams in implementing and adhering to established automation standards.
  • Ensure consistency and quality of automation deliverables including requirements, functional specifications, control strategies, phases, and recipes.
  • Define or review software components that require development or modification.
  • Contribute to the preparation and review of PTO deliverables.
  • Offer technical consulting and guidance as part of the PTO team.
  • Collaborate with cross-functional stakeholders to ensure deliverables meet business and regulatory needs.
  • Maintain compliance with required training and quality standards.

Requirements:

  • Bachelors degree in Engineering or equivalent experience.
  • 10+ years of automation experience in the pharmaceutical industry (preferably API or drug substance manufacturing).
  • Proven experience in leading or delivering large-scale automation projects.
  • Minimum 5 years of hands-on experience with DeltaV Batch DCS.
  • Minimum 3 years of experience with Allen-Bradley PLCs.
  • Experience with Aveva PI (OSIsoft PI) preferred.
  • Strong understanding of GMP, regulatory requirements, and computer system validation (CSV) principles.
  • Excellent teamwork, communication, and stakeholder management skills.

About the job

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Job type

Full Time

Experience level

Education

Bachelor degree

Experience

10 years minimum

Experience accepted in place of education

Location requirements

Hiring timezones

United States +/- 0 hours

About Advanced Manufacturing Tech Solutions (AMTSOL)

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Advanced Manufacturing Tech Solutions (AMTSOL) delivers innovation through technology for life science manufacturing, with a focus on Pharma 4.0 and digitalization. They help regulated manufacturers increase speed to market and operating efficiency through end-to-end implementation and support of GMP manufacturing systems. Their expertise spans Automation, Manufacturing Execution Systems (MES), OT Networking, and Digital Technologies for pharmaceutical and biotech manufacturing environments.

AMTSOL operates as a vendor-independent solutions provider, taking a fully responsible approach as a single partner for consultancy, project support, and continuous improvement. Their integrated approach covers Level 2 to Level 5 solutioning, from automation systems through cloud integration and data analytics. The company partners with global pharmaceutical and biotechnology organizations across Singapore, Europe, and the USA to deliver automation, MES, CSV, CQV, and digital transformation solutions with an emphasis on GMP compliance, data integrity, and operational excellence.

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