Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Parental leave
- Vision insurance
- Wellness resources
Company
Crystal Pharmatech, Inc. is a technology-driven CRO based whose services range from solid state information to processing for active pharmaceutical ingredients and formulations. Crystal Pharmatech provides clients with data derived from experiments and partners with clients to ensure comprehensive solutions for their research needs based on sound scientific understanding. www.crystalpharmatech.com
Job Description
The successful candidate will handle all areas of solid-state research applied to API with a strong emphasis on early formulation development. The candidate will develop experimental designs under the supervision of the immediate manager. The candidate must actively communicate across multiple functional areas including process chemistry, analytical chemistry and physical chemistry. The candidate will be given appropriate training before handling a new task.
The ideal candidate should have the following qualifications:
The ideal candidate should have the following qualifications:
- MS in Chemistry, Pharmaceutical Science or related field
- Industry experience: 1-2 years of experience with a Master’s degree in related field
- Display a high-level of innovation and practical ingenuity
- A background in topics including thermodynamics, polymorphism, crystallization, API and formulation process development
- Always diligent in scientific rigor displaying a high-level of integrity
- Strong communication and interpersonal skills required to effectively collaborate with team members and clients
- Strong scientific writing skills.
Work Location:
This position is based onsite at our Cranbury, New Jersey facility. This role requires regular onsite laboratory work and is not eligible for remote or hybrid arrangements.
This position is based onsite at our Cranbury, New Jersey facility. This role requires regular onsite laboratory work and is not eligible for remote or hybrid arrangements.
Roles and Responsibilities
- Crystal form screening, scale-up, full characterization and evaluation
- XRPD, DSC, TGA, PLM, KF, GC, HPLC use and data interpretation
- Good organization skills
- Able to multitask and maintain multiple projects at one time
Recruiter Notice:
This position is not open to third-party recruiters or staffing agencies. Unsolicited resumes will not be accepted and do not constitute a contractual relationship.
This position is not open to third-party recruiters or staffing agencies. Unsolicited resumes will not be accepted and do not constitute a contractual relationship.
Compensation: $75,000.00 - $78,000.00 per year
About Us
Crystal Pharmatech, established in 2010, is a global company with approximately 300 employees and three R&D centers located in Suzhou (China), New Jersey, San Francisco (USA), and Toronto (Canada). Our key differentiator is our integrated and specialized services, including API solid-state research, crystallization, preformulation, formulation development and manufacturing, clinical supply.
Our Company
Crystal Pharmatech, established in 2010, is a global company with approximately 300 employees and three R&D centers located in Suzhou (China), New Jersey, San Francisco (USA), and Toronto (Canada). Our key differentiator is our integrated and specialized services, including API solid-state research, crystallization, preformulation, formulation development and manufacturing, clinical supply.
Our Company
Crystal Pharmatech, established in 2010, is a global company with approximately 300 employees and three R&D centers located in Suzhou (China), New Jersey, San Francisco (USA), and Toronto (Canada). Our key differentiator is our integrated and specialized services, including API solid-state research, crystallization, preformulation, formulation development and manufacturing, clinical supply.
With an average of 20 years of experience, our scientific leadership team has successfully delivered over 100 early phase and 19 commercialized products for global pharmaceutical companies. We have served over 1,000 clients, supporting more than 2,000 new chemical entities.
Leveraging our unique expertise, we collaborate with you to design and develop the most suitable crystal form and formulation for further development. Our guiding principle of "getting the crystal form and formulation right the first time for Phase I" not only expedites the progression of your molecule to IND filing and Phase I clinical trials, but also minimizes the necessity for human PK bridging studies. This approach saves valuable time and reduces costs as your program moves forward to Phase II or subsequent clinical trials.



