Skills Alliance
Overview
Are you an experienced DeltaV Engineer looking to take the next step in your career? We are seeking skilled professionals to join a growing automation team supporting cutting-edge life science projects in Indiana, US. They are looking to grow their team due to project demand.
Location Indiana, United States (Hybrid)
Experience 10+ years working Automation experience in the Pharmaceutical Industry.
Role Contract project based role, Duration of 2 years.
Structure Hybrid - Minimum 2 weeks a month in Indiana during the first 6 months of the assignment and minimum 1 week a month for the remaining 18 months.
About the Role This role is responsible for the automation philosophy, Program technical standards and ensuring consistency throughout the projects. You will play a key role in supporting and providing oversight to the individual project teams. The software lead will be responsible for an individual projects oversight and contribute technically to the deliverables.
Key Responsibilities
Technical oversight of a project within the Foundry program.
Working closely with the Project Technical Team to ensure the automation solution is aligned with the overall program automation philosophy and standards.
Collaborate with their Digital/MES workstream counterpart leads to align the automation and digital solutions.
Provide technical support/oversight to the project team to ensure that applicable standards are followed.
Ensure consistency of the automation deliverables (requirements, functional specifications, control strategies, phases, and recipes, etc.).
Assist in defining the software components that need to be created or modified.
Interface with other disciplines and stakeholders to ensure the deliverables meet business needs.
Maintain compliance with training requirement.
Requirements
10+ years working Automation experience in the Pharmaceutical Industry (preferable in API/drug substance manufacturing).
Previous experience in the delivery of large Automation Projects in the Pharmaceutical Industry.
5+ years of experience in DeltaV Batch DCS.
3+ years of experience with Allen-Bradley PLCs.
Preferable, previous experience with Aveva PI.
Exceptional teamwork abilities.
Strong knowledge of GMP’s, regulatory requirements and computer system validation principles.
Excellent written and verbal communication skills for both technical and non-technical audiences.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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Location Indiana, United States (Hybrid)
Experience 10+ years working Automation experience in the Pharmaceutical Industry.
Role Contract project based role, Duration of 2 years.
Structure Hybrid - Minimum 2 weeks a month in Indiana during the first 6 months of the assignment and minimum 1 week a month for the remaining 18 months.
About the Role This role is responsible for the automation philosophy, Program technical standards and ensuring consistency throughout the projects. You will play a key role in supporting and providing oversight to the individual project teams. The software lead will be responsible for an individual projects oversight and contribute technically to the deliverables.
Key Responsibilities
Technical oversight of a project within the Foundry program.
Working closely with the Project Technical Team to ensure the automation solution is aligned with the overall program automation philosophy and standards.
Collaborate with their Digital/MES workstream counterpart leads to align the automation and digital solutions.
Provide technical support/oversight to the project team to ensure that applicable standards are followed.
Ensure consistency of the automation deliverables (requirements, functional specifications, control strategies, phases, and recipes, etc.).
Assist in defining the software components that need to be created or modified.
Interface with other disciplines and stakeholders to ensure the deliverables meet business needs.
Maintain compliance with training requirement.
Requirements
10+ years working Automation experience in the Pharmaceutical Industry (preferable in API/drug substance manufacturing).
Previous experience in the delivery of large Automation Projects in the Pharmaceutical Industry.
5+ years of experience in DeltaV Batch DCS.
3+ years of experience with Allen-Bradley PLCs.
Preferable, previous experience with Aveva PI.
Exceptional teamwork abilities.
Strong knowledge of GMP’s, regulatory requirements and computer system validation principles.
Excellent written and verbal communication skills for both technical and non-technical audiences.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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