Engineer III - API Crystallization - FSP

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New Jersey
Pharmaceutical
The Role

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 an Engineer 3 position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off.  This position does not offer any sponsorship.

Overview / Responsibilities

The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control.  Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.).  The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department.

Qualifications

  • BS or MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required

  • Engineer 3, MS plus 1-2 years’ experience in a regulated work environment, or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities; BS with 3-5 years.

Required Skills and Experience

  • Knowledge of chemistry theory and practice, along with process scale-up

  • Ability to work in the lab with a variety of chemicals

  • Experience in wet chemistry including safely handling solvents and chemicals, running experiments, proper disposal of waste, and generating and analyzing data

  • Ability to use an array of characterization instruments

  • Good organizational, interpersonal, writing, and time management skills

  • The ability to strictly follow established procedures, policies and guidelines required to comply with safety, environmental and GMP expectations in the lab

  • Initiative and independence to develop, apply, and/or improve new systems and best practices

  • The ability to work independently with a minimum of supervision and as part of teams when required

  • Ability to work accurately in a fast-paced environment

  • Ability to write clear and concise reports

  • Familiarity with MS Office products

  • Proficiency with computers and experience with local and web-based software

  • Ability to integrate into the existing work and culture

Desired Skills and Experience

  • Experience in crystallization and/or with using Mettler Toledo equipment (i.e., Easymax / Optimax reactor systems)

  • Experience with in-situ or off-line analytical techniques such as FTIR, FBRM, PVM, Raman, and/or GC/HPLC

  • Experience with solids handling within a ventilated balance enclosure

  • Familiarity with statistical experimental design (i.e., Design of Experiments)

  • Flexibility to adapt to changing work assignments and deadlines

  • Firsthand experience with experiments and data analysis using Differential Scanning Calorimetry (DSC) or other calorimetry techniques and tools

  • Experience with mathematical modeling using Aspen, MATLAB / Mathematica or similar

#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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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

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