Sr Validation Scientist (Rincon)

Employment Type

: Full-Time


: Engineering

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QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, youll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico.

You'll be a fit for this job if you have:
  • Bachelors degree in Life Sciences or Engineering (preferred)
  • 5 years of related experience
  • Fully Bilingual English/Spanish Written is required
In this position you'll:
  • Independently provides and/or directs the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or manufacturing support environment.
  • Able to troubleshoot systemic validation issues.
  • Applies advanced and diverse validation engineering principles to the design and implementation of major system or process modifications and/or capital projects.
  • Develops, organizes, analyzes and presents interpretation of results for operational issues or validation engineering projects of significant scope and complexity.
  • Complete complex or novel assignments requiring development of new and/or improved validation engineering techniques and procedures.
  • Develop validation engineering policies and procedures that affect multiple organizational units.
  • Supervise, coordinate and review work of a small staff of engineers and/or technicians on an ongoing basis as well as on a project basis.
  • Employ advanced validation engineering techniques and/or modifications of advanced techniques within area of validation engineering expertise.
  • Apply knowledge of validation engineering principles and practices outside of area of expertise to broad variety of assignments in related fields.
  • Work with manufacturing, process development, utilities, facilities, labs, and/or quality assurance in developing requirements and recommendations for large and/or highly complex process, system/facility modifications.
  • Work with project managers to complete the validation responsibilities of engineering projects within schedule, budget and quality constraints.
  • Develop departmental budgets or project budgets encompassing multiple disciplines for area within project or entirety of smaller project.
To get hired at QUALITY CONSUTING GROUP, you MUST be:
  • Parenteral Process Validations, vial or syringe filling.
The details:
  • We're a growing 60+ person company.
  • We are actively looking for the best candidate.
  • We accept applications and RESUMEs
Positions Available: One (1)

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Associated topics: bioengineering, bioinformatic, biological engineer, biomaterials, biomedical, biomedical engineer, biophysics, bioprocessing, fermentation, therapeutic

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