Process Chemist

2 weeks ago

South Plainfield, United States TPG Staffing, LLC Full time

TPG Staffing LLC is a leading national staffing agency providing businesses and job applicants with quality opportunities in a wide range of industries. We believe in getting the right person for the right job and the right job for the person. We work closely with our clients to build relationships based on understanding the key drivers of their businesses and the talent required to meet their business goals while providing job seekers with rewarding experiences to enrich their careers.

Our client Located in Central NJ is seeking a Process Chemist to join their growing team. We are seeking a highly motivated and skilled Process Chemist to join our Process R&D Department. In this role, you will be responsible for the development, optimization, and scaling of chemical processes for pharmaceutical production. You will collaborate with cross-functional teams to ensure that our processes are efficient, cost-effective, and compliant with regulatory standards. This job description applies to activities and responsibilities associated with the process chemistry development group and support of GMP Operations.

Prerequisites

  • MS in chemistry
  • Pharmaceutical/biotechnology industry or CDMO industry is required.

Responsibilities

  • Follow existing synthetic routes, making processing improvements where necessary, while conducting multi-step organic synthesis
  • Plan and organize routine operations to maximize production output.
  • Design novel synthetic routes and carry out multi-step organic synthesis.
  • Operate simple open access HPLC/UV, LC/MS, MS, NMR, GC/MS, and other analytical instruments required to monitor reaction processes.
  • Consult with management, the Analytical Department, the Director of GMP Operations and others on issues concerning experiments prior to and during GMP production.
  • Accurately make and check calculations, prepare raw materials, reagents and solutions in accordance with company SOP's.
  • Faithfully record procedures and results in Batch Records or Solution Preparation Forms, notebooks, or other appropriate forms in an organized manner as dictated by departmental SOP and GMP regulations.
  • Write reports on research as required.
  • Promote compliance with cGMP regulations. Attend GMP training sessions.
  • Support management and maintenance of the SOP and Document Control system.
  • Work with clients to develop material release tests and specifications for materials
  • Help ensure that client project needs, requirements, and timelines are communicated to, and coordinated between, GMP Operations and Quality Control. • Conduct process chemistry R&D for clients as an individual contributor, which includes, but is not limited to, research on synthetic routes to active pharmaceutical ingredients and chemical intermediates by route discovery, process optimization, safety evaluation, enabling technologies, high throughput screening and chemo/biocatalytic reaction discovery and optimization. This will include R&D under c-GLP and potentially under c-GMP conditions.
  • Develop safe, timely and efficient chemical processes by using established, new and/or novel chemical methodologies and processes.


Qualifications:

  • Required a Bachelors or Masters in Organic Chemistry.
  • Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects.
  • Knowledge and experience base of working in a c-GMP environment is preferable, but not required
  • Excellent written, verbal and presentation skills.
  • Experience in small molecule drug development is preferable, but not required.
  • Track record of scientific success as measured by publications and presentations.
  • Ability to prioritize and manage numerous activities simultaneously.
  • Ability to interact in an effective and appropriate manner with diverse population sets.
  • Experience in working on and positively contributing to scientific teams.
  • Ability to perform the physical requirements of the position.


The above requirements and qualifications are meant to describe the general nature of the position and do not represent all duties to be performed by the selected candidate. Please note that only candidates who are under consideration for the position will be contacted. The Company is an equal opportunity employer. All employment is decided on basis of qualifications, merit, and business needs without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or veteran or disability status.

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