Jobs › Companies › Parexel › Senior Scientist I or Scientist III - Analytical Chemist (Drug Product) - FSP

Sobre esta vaga de Senior Scientist I or Scientist III - Analytical Chemist (Drug Product) - FSP na Parexel

Parexel · Híbrido · United States - New Jersey - Client Onsite

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are looking to fill a Scientist 3 or Senior Scientist I -Analytical Chemist (Drug Product) position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ.  This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. 

Qualifications - B.S./M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience as listed below in a GMP laboratory environment.

 

  • Scientist 3 - B.S. with 3-5 years of experience; M.S. with 1-2 years of experience
  • Senior Scientist - B.S. with 5+ years of experience; M.S. with 2+ years of experience

 

Required Skills and Experience

  • Hands-on experience with chromatographic analysis using various UPLC, HPLC and GC techniques, including method and instrument troubleshooting
  • Consistently adheres to GDP standards with accurate, compliant documentation
  • General knowledge of separations science
  • General understanding of analytical method development and method validation
  • Hands-on experience with FTIR, KF and Dissolution
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Excellent organization to multi-task and manage multiple ongoing projects in parallel including GMP release, stability testing along with data processing, interpretation and reporting
  • Ability to work independently and as part of a team, displaying self-motivation, adaptability, and a positive attitude
  • undefined Desired Skills and ExperienceEmpower softwareAnalysis of drug product and drug substance

About Parexel

Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.


For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.


Come join us!


#LI-DK1

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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Sobre a Parexel

Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies a

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