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HPLC Chemist-3544-FSP

Quakertown, Pennsylvania, United States Date posted 09/13/2021 Job ID 74836BR

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Success Profile

Check out the top traits we're looking for and see if you have the right mix.

  • Detail-Oriented
  • Proactive
  • Problem-Solver
  • Results-Driven
  • Organized
  • Multi-Tasker
  • "When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."

    Chris – Associate Director, Regulatory & Access
  • "In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"

    Riley – Regulatory Affairs Consultant

Rewards

  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Management

    Strong management with depth of experience working for global health authorities.

Responsibilities

Qualifications
  • BS degree and 1-2 years of experience, or
  • MS degree with no experience
Required Skills and Experience
  • Some experience with chromatographic analysis using various UPLC and HPLC techniques
  • General knowledge of separations science
  • Hands-on experience in chromatographic analysis
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Excellent organization to multi-task and manage multiple projects
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Desired Skills and Experience
  • Experience with Empower chromatographic data program and with analysis of drug formulations preferred.
  • Good understanding of GLP or GMP compliance requirements and ALCOA documentation principle
Responsibilities
  • Conducting analyses of dose formulations used in preclinical studies
  • Data interpretation and processing
  • Being responsible for following safe laboratory practices and for maintaining the work area in a clean orderly and safe manner
  • General understanding of analytical method development and method validation

Qualifications

Qualifications
  • BS degree and 1-2 years of experience, or
  • MS degree with no experience
Required Skills and Experience
  • Some experience with chromatographic analysis using various UPLC and HPLC techniques
  • General knowledge of separations science
  • Hands-on experience in chromatographic analysis
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Excellent organization to multi-task and manage multiple projects
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Desired Skills and Experience
  • Experience with Empower chromatographic data program and with analysis of drug formulations preferred.
  • Good understanding of GLP or GMP compliance requirements and ALCOA documentation principle
Responsibilities
  • Conducting analyses of dose formulations used in preclinical studies
  • Data interpretation and processing
  • Being responsible for following safe laboratory practices and for maintaining the work area in a clean orderly and safe manner
  • General understanding of analytical method development and method validation

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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