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Sr Automation Engineer
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Sr Automation Engine....
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Sr Automation Engineer

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1 Vacancy
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Jobs by Experience

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5years

Job Location

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Novato - USA

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2855147

Sr Automation Engineer

Location: Novato CA (Hybrid)

Duration of Contract: Long term Starts Immediate runs through March 2027 with possible extension


Responsibilities

  • Implement capital automation projects using industry best practices and company business processes.
  • Support the scope deliverables schedule and project team for capital expenditure (CapEx) of automation projects.
  • Participate in the development and evaluation of RFP and bidder/vendor analysis for General contracting and engineering services when design build method used.
  • Works directly with project controls to prepare and update project status schedule resource and cost reports within Oracle based tools (OPPM & P6) for the use of numerous BMRN departments.
  • Identify and oversee system integrations.
  • Ensure consultants & contractors working on any automation related projects maintain compliance with all GMP requirements (including training) EHS&S and security requirements including completion and review of Job Hazard Assessments and company policies.
  • Coordinate/support engineering and automation design commissioning qualification and the QA
  • Validation groups as appropriate.
  • Proactively look for and recommend improvements in site processes and procedures.
  • Represent the Capital Project Automation group with good communication and presentationskills.
  • Provide status reports on Projects to Automation Management as required.

Requirements

Requirements

  • Minimum 10 years of automation engineering experience preferably in the biotech or pharmaceutical organization.
  • Experience with Emerson DeltaV Process Control System (PCS)
  • Ability to work with minimal direct supervision: meet deadlines prioritize assignments provide recommendations and effectively communicate updates.
  • Experienced with communicating with in supporting Executive Management as well as providing direction support for multiple projects simultaneously.
  • Must be very organized and possess strong verbal and written communications skills.
  • Must be proficient with Internet navigation Microsoft Office (Outlook Word PowerPoint Excel Project Teams Sharepoint) Adobe Acrobat
  • Should be flexible to working outside the core business hours (occasionally on short notice and a limited basis) as needed.
  • Proven ability to manage multiple and fastmoving priorities.
  • Ability to work well in a fastpaced collaborative team environment within a rapidly evolving business environment.
  • Skilled at solving multidimensional problems with both quantitative and qualitative variables.
  • Ability to lead and influence others in support of company objectives.
  • Excellent decision making and cross functional team building skills.
  • Solid understanding of GMP GLP and nonGMP project requirements
  • Able to read and understand engineering plans and specifications.
  • BS degree from an accredited university in a construction or engineering related field.
  • Could be a combination of AS degree and industry experience.


Minimum 10 years of automation engineering experience preferably in the biotech or pharmaceutical organization. Experience with Emerson DeltaV Process Control System (PCS) Ability to work with minimal direct supervision: meet deadlines, prioritize assignments, provide recommendations and effectively communicate updates. Experienced with communicating with in supporting Executive Management as well as providing direction support for multiple projects simultaneously. Must be very organized and possess strong verbal and written communications skills. Must be proficient with Internet navigation, Microsoft Office (Outlook, Word, PowerPoint, Excel, Project, Teams, Sharepoint), Adobe Acrobat Should be flexible to working outside the core business hours (occasionally on short notice, and a limited basis) as needed. Solid understanding of GMP, GLP, and non-GMP project requirements Able to read and understand engineering plans and specifications. BS degree from an accredited university in a construction or engineering related field.

Employment Type

Full Time

Company Industry

Pharma / Biotech / Clinical Research

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