drjobs Sr. Automation Engineer

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Manatí - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Provides support to the automation and computerized systems in Manufacturing and Utilities Areas.

WHAT MAKES YOU A FIT:

The Technical Part:

  • BachelorsDegree inScience with (5) years of experiencein electrical computer mechanical engineering andrelated fields.
  • CommunicationSkills
  • Shift: Administrative and according to business needs.
  • Experience in:
    • Process Automation CSV investigations and deviations.
    • Troubleshooting (SCADA/PLC).
    • FDA regulatory compliance (internal and external).
    • Project Management for validations and qualifications.

The Personality Part:

  • Being self-motivated means that you are curiousand anxious to explore all possibilities without anyone telling you to (while also following instructions of course). It means youre creative with such an eye for detail that nothing gets past you. If this sounds like you and if you have a commitment to serving customers with high-quality research and products to embracing a diverse work culture and even to the environment you might just be what were looking for!

AS A PIECE OF FITS YOU WILL: (The day-to-day on the job)

  • Proficient knowledge of computer system life cycle concepts change control systems and FDA regulatory requirements including 21 CFR Part 11.
  • Proven experience issuing and preparing Computerized Functional Requirements and Design Specifications.
  • In-depth knowledge of the science and physics involved in designinginstalling commissioning and validation/qualification of computerized systems and PLCs as applied to pharmaceutical production environments.
  • Broad knowledge of relevant governmental regulations cGMPs and guidelines abouta biopharmaceutical manufacturing plant.
  • Experience with external and internal regulatory audits (FDA EMA Otsuka Sanofi etc.
  • Knowledge of pharmaceutical business processes and equipment.
  • Knowledge of mechanical concepts electrical controls theory and electronic circuitry.
  • Proven skills in projectmanagement systems development and implementation of manufacturing MES Systems and quality-relatedsystems.
  • Ability to manage and operate computer software packages used for data acquisition systems and PLC programming including (not limited to) Rockwell Automation platform visualization and programming solutions/tools.
  • Knowledge of data historian (including but not limited to OSI PI-FactoryTalk Historian) Databases (MS SQL) and networking infrastructure and topologies.

WHO WE ARE:

We are a serviceprovidercompany that is different from the rest. We pride ourselves in how we treat the most important piece of our companys puzzle: you! We integrate Engineering Construction Maintenance Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible family-oriented and focused on the well-being of our resourceswhile providing our pharmaceutical medicaldevice and manufacturingindustryclients with top-notch quality talent.Were FITS!

Are you the Next Piece


Required Experience:

Senior IC

Employment Type

Contract

Company Industry

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.