Job Title: Analytical Scientist III

Job Location: Boothwyn, PA.

Job Summary:

The Analytical Scientist III is responsible for coordinating the chemical method projects in the analytical department. Specific duties will include:

  • Conduct material characterization and physical testing and will support process development and manufacturing. She/he will conduct stability evaluation, and API/raw material, in-process and finished product release testing.

  • Serve as Project Leader for assigned projects and act as a technical liaison with Clients to provide written/verbal reports on progress or changes to plan.

  • Coordinate the project activity schedule to ensure that all the activities are assigned appropriately and completed on time.

  • Author, review and approve reports, SOPs and protocols as needed.

  • Work closely with Formulation Development and Quality Assurance departments to meet all Client and QS Pharma technical milestones.

  • Participate in initial discussions with potential clients. Work closely with Business Development to provide Client presentations, tours, preparation of development work plans, prepare/review proposals to support current clients and new business opportunities.

  • Develop and implement training program for the department personnel.

  • Carry out duties in compliance with all state and federal regulations and guidelines including FDA, EPA, OSHA and DEA. Comply with all company and site policies and procedures.

  • Minimum requirements:

    Master’s degree in Chemistry, Pharmacy, or related field, or foreign degree equivalent, plus 2 years of industrial pharmaceutical laboratory experience.

    The experience (which may be gained concurrently) must include:

  • Demonstrated scientific, technical, and regulatory proficiency in the area of Analytical Research & Development including liquid chromatography development, troubleshooting, sample preparation and method validation;

  • Experience with creating SOPs related to testing of the drug development in various phases of development, from preclinical to commercial;

  • Experience working in compliance with FDA, EPA, OSHA and DEA regulations.

  • To apply send resume and letter of application detailing experience to Jenne’ Johnson, HR Generalist, QS Pharma LLC, 3 Chelsea Parkway, Boothwyn, PA 19601;