Analytical Technical Services

hace 4 semanas


Manatí, Puerto Rico MyKelly A tiempo completo
Kelly® Science & Clinical is seeking Analytical Technical Services for a 8 month contract position at a Global Pharmaceutical client in Manati, Puerto Rico.  If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Salary: $38.79  per/hour

Overview

This client is Global Biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

In this role you’ll be responsible for designs, executes and evaluates method development protocols to ascertain the required degree of validation for new and existing methods guaranteeing implementation of a feasible, efficient, rugged, and robust method.

This role will give you an opportunity to transform patients’ lives through science by contribute with a global leading biopharma company powered by talented individuals who drive scientific innovation.

Schedule: Office hours, but with the flexibility that we are working with projects and the hours can be extended.

Responsibilities:
  • Designs, executes and evaluates method development protocols to ascertain the required degree of validation for new and existing methods guaranteeing implementation of a feasible, efficient, rugged, and robust method.
  • Supports technical aspects of test method ruggedness and robustness processes.
  • Supports the Analytical Ruggedness Project Manager and Quality Control to gather information on investigations, troubleshooting, method deviations, method optimization, and method change control.
  • Leads analytical special projects to accomplish company goals and objectives on a timely and effective manner.
  • Support laboratory instrument qualification including knowledge in Maximo, Infinity
  • Generate IOQ and PQ reports for the qualification of Analytical Instruments
  • Provides timely and efficient technical reports to document all analytical improvement or investigation projects.

Qualifications:
  • BS Degree with five (5) years experience in pharmaceutical industry with at least two (2) years experience in method development/transfer of biomolecules.
  • At least two (2) years experience in method development/transfer of biomolecules.
  • Technical Skills: Equipment Validation Expertise (URS, DQs, Validation Master Plan PQ). Maximo application user. Infinity application user.
  • Fully bilingual (Spanish/English) communication skills, both written and verbal.
What happens next:
 
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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