drjobs Technical Project Lead

Technical Project Lead

Employer Active

1 Vacancy
The job posting is outdated and position may be filled
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

Bend, OR - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Schedule

Standard (MonFri)

Environmental Conditions

Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc. Standing for full shift

Job Description

Thermo Fisher Scientific invests over $1 billion yearly in R&D supporting groundbreaking discoveries.

Location/Division Specific Information

Bend Oregon site specializes in developing solid oral dosage formulations for small molecule clinical trials.

How will you make an impact

Lead the design and evaluation of formulations and manufacturing processes for clinical studies.

What will you do

  • Lead research scientist/engineer for design evaluation and scaleup of novel formulations. Own technical aspects for project lifecycle acting as main technical contact for client projects.
  • Assess technical data to develop knowledge sets aid decisionmaking and lead problemsolving for formulations equipment and processes.
  • Develop protocols for formulation work aid in producing manufacturing batch records for clinical trial materials and review technical documents.
  • Apply craft knowledge of core OSD technologies to meet client deadlines for drug development.

How will you get here

Education

  • Masters or Ph.D. degree in pharmaceutics/pharmaceutical science engineering or a physical or biological science preferred.
  • Bachelors degree also acceptable with more years of experience.

Experience

  • 25 years working in pharmaceutical development/manufacturing or related industry preferably with solid oral dosage forms
  • Good knowledge of or ability to quickly learn Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs)
  • Proven ability to work on multiple projects simultaneously using good time management skills
  • Preferably experience with statistics process control computer programming and risk management

Knowledge Skills Abilities

  • Excellent written interpersonal and presentation skills
  • Decisive and selfmotivated
  • Outstanding attention to detail
  • Excellent planning and organization skills; effective time management and prioritization to lead multiple projects simultaneously
  • Comfortable working in demanding fastpaced environment

Required Experience:

Senior IC

Employment Type

Full-Time

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.