Scientist III, Technical Project Lead, Drug Formulation

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profile Job Location:

Bend, OR - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Laboratory Setting Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Standing for full shift Strong Odors (chemical lubricants biological products etc.) Will work with hazardous/toxic materials

Job Description

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Are you prepared to take your research career to the next level At Thermo Fisher Scientific Inc. youll have the opportunity to work on groundbreaking projects that make a real difference in the world! With a strong focus on innovation and collaboration we aim to compose an encouraging and inclusive environment where your expertise can flourish.

Location/Division Specific Information

Located in Bend Oregon our site leads in solubilization at Thermo Fishers Pharma Services Group. We specialize in crafting small molecule oral dosage forms for early clinical trials employing modern techniques such as hot-melt extrusion and spray-drying.

How will you make an impact

Lead the development and assessment of product formulas and production methods for research projects.

What will you do

  • Serve as the primary research scientist/engineer supporting development evaluation and scale-up of novel formulations.
  • Act as the technical owner of projects partnering with Project Managers and Analytical Leads.
  • Evaluate and interpret technical data to support decision making and problem solving.
  • Develop protocols for formulation development assist with production of clinical trial materials and author technical documents.

You will bring to bear your knowledge of core OSD technologies to meet client timelines and mentor team members in formulation and process development.

How will you get here

Education

  • Masters or Ph.D. in pharmaceutics engineering or a related science. Bachelors degree or equivalent experience in the field is also considered.

Experience

  • Experience of 2-5 years in pharmaceutical development/manufacturing with a preference for solid oral dosage forms.
  • Knowledge of GMP and SOPs.
  • Proficiency in handling various projects while demonstrating robust time management capabilities.
  • Preferably experienced in statistics process control and risk management.

Knowledge Skills Abilities

  • Excellent written interpersonal and presentation skills.
  • Self-motivated with outstanding attention to detail.
  • Proficient in effective planning organization and time management abilities.
  • Comfortable in a fast-paced demanding environment.


Required Experience:

Senior IC

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Laboratory Setting Office So...
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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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