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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Principal Scientist 1, 2 Synthetic Chemist, Process Development Engineering & Safety - FSP

Job ID R0000039654

We are looking to fill a Principal Scientist position working as a full-time employee of Parexel FSP on 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 sponsorship.

Description

The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ is seeking a motivated and technically focused chemist who is looking for an opportunity to develop and optimize chemical process steps combining a series of typical chemical engineering unit operations used in the specialty chemical and pharmaceutical industries (e.g. reactions, extractions, distillations, crystallizations, filtrations, drying).  The individual would do this as part of project teams working together on chemical processes combining multiple chemical steps in order to bring new active pharmaceutical ingredients (APIs) through the R&D pipeline from early through late-stage development.

This position is largely a laboratory-based role to support chemical process development performed at scales spanning the range from grams to multi-kilogram scale in order to understand scale-up issues, improve process robustness, quality, safety, environmental footprint and yield, troubleshoot issues, optimize, and deliver process intermediates and/or APIs. This role requires the ability to work in the lab with a variety of chemicals, use an array of manual and automated laboratory reactors/equipment and process/analytical instruments.  Deskwork will involve planning, analysis, and documentation of laboratory experiments, and writing clear and concise reports.  The role offers fast-paced, hands-on research that requires a high degree of technical skills and contributions.

Qualifications

  • Principal Scientist I - PhD in Chemistry or closely related field (Biochemistry, Analytical Chemistry, Research Sciences, Material Sciences, etc.); or MS degree in Chemistry or a closely related field (Biochemistry, Analytical Chemistry, Research Sciences, Material Sciences, etc.) with 3+ years of professional experience in pharma/biopharma industry.

  • Principal Scientist II - PhD with 1-3 years of experience in in pharma/biopharma industry (can include post doc), or MS degree with 5+ years of professional experience (as stated above).

Required Skills and Experience

  • Demonstrated experience with chemical process development, scale-up, and unit operations including reactions, extractions, distillations, crystallizations, filtrations, and drying.

  • Strong laboratory skills with the ability to safely handle a wide variety of chemicals, execute experiments, and generate, analyze, and document data in compliance with safety and Good Laboratory Practices (GLP) expectations.

  • Knowledge of chemistry theory and practice, including process robustness, quality, yield, and environmental considerations.

  • Ability to work accurately and safely in a fast-paced, regulated laboratory environment with minimal supervision.

  • Proficiency with computers and experience using local and web-based software tools (e.g., MS Office, data analysis tools).

  • Strong organizational, interpersonal, written, and oral communication skills to effectively collaborate within cross-functional project teams.

  • Demonstrated ability to follow established procedures, policies, and guidelines to meet safety, environmental, and quality requirements.

  • Initiative and independence to develop, apply, and improve laboratory systems, methods, and best practices.

Desired Skills and Experience

  • Hands-on experience with laboratory reactor and process equipment, including automated systems such as Mettler Toledo EasyMax/Optimax.

  • Experience using in-situ or off-line analytical and characterization techniques such as HPLC, GC, FTIR, Raman, FBRM, PVM, KF, or DSC.

  • Familiarity with statistically designed experimentation, including Design of Experiments (DoE) methodologies.

  • Experience with API crystallization, isolation, drying, and particle physical attribute control at bench and kilo-lab scales.

  • Awareness of current Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP).

  • Experience with process safety evaluations, calorimetry, hazard analysis (e.g., PHA, LOPA), or environmentally sound process design.

  • Exposure to mathematical modeling, data analysis, or simulation tools (e.g., Aspen, MATLAB, Mathematica or similar).

  • Experience with PHA's, Layers of Protection Analysis or similar risk evaluation methodologies.

  • Flexibility to adapt to changing work assignments, priorities, and project timelines.

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!

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