Job Title: Analytical Scientist III
Job Location: Boothwyn, PA.
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.
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; firstname.lastname@example.org.