Located in beautiful Chenango County near the Finger Lakes and Adirondack regions, we offer first rate scientific careers in a bucolic setting, with affordable housing, excellent schools and many recreational opportunities such as canoeing, hiking, swimming, and skiing. The cities of Ithaca, Binghamton, Syracuse and Albany are all within 1 - 1.5 hours drive, offering unique cultural opportunity within the region.
We seek professionals who thrive on independent thinking and continual professional development. We offer a competitive employment package that includes full medical and dental, and generous, flexible vacations.
Please submit a cover letter and your resume by email to:
HR@pharmassistlab.com
Job Opportunities at PharmAssist: Posted September 5, 2006
Scientist
PharmAssist Analytical Laboratory has an immediate opening for a Research and Development Scientist. The qualified candidate will develop and validate analytical methods for API and related compounds in drug products and drug substances/raw materials. Previous experience with experimental design, formulation development studies, forced degradation and stability studies desired. Must be familiar with cGMP regulations, FDA, and ICH guidelines. Should have excellent knowledge of chemistry, liquid and gas chromatography, dissolution and wet chemistry. Good understanding of USP and other compendia procedures and requirements is also necessary. Knowledge of IQ/OQ/PQ of laboratory instrumentation and equipment, experience in writing SOP's, method development reports, validation protocols and validation reports.
Requires: This position requires a Ph.D in analytical chemistry, a Masters degree in Chemistry plus 2 years of pharmaceutical analysis experience, or a BS degree in Chemistry plus 3 years of pharmaceutical analysis experience with a strong knowledge of HPLC. Plan and organize work with minimal supervision, interpret analytical data in regards to acceptability and consistency. Must be computer literate in Word, Excel and Power Point.
Scientific Data Reviewer
The Scientific Data Reviewer functions as a peer review of raw data and documentation-related work for R&D projects. This individual will have sound scientific judgment and expertise in cGMP requirements directly related to analytical testing. He/she will review data packets to ensure that all steps have been performed and verified and appropriately investigated where applicable. Applicants must be able to plan and organize work with minimal supervision, interpret analytical data in regards to acceptability and consistency. He/she will also ensure that the data meets internal QA and Sponsor compliance standards and participate in the preparation of progress reports regarding the status of the project.
Requires: This position minimally requires a BS degree in a scientific discipline and 3+ years of pharmaceutical industry experience. Other requirements include a deep understanding of analytical technologies (HPLC, GC, UV Spectroscopy) and method validation requirements, as well as a demonstrated ability to manage multiple projects and meet critical deadlines. Candidates must have excellent written and verbal communication skills, demonstrated ability to work in a team-oriented environment, and strong interpersonal skills. Must be computer literate in Word, Excel, and Power Point. Work schedule may be flexible.
QA Associate
PharmAssist Analytical Laboratory has an immediate opening for a Quality Assurance Associate. The QA group is responsible for assisting in all QA and regulatory affairs, including but not limited to document review and control, regulatory compliance training, and internal/external audits. The QA Associate addresses all quality issues and leads in the development/establishment/maintenance of the laboratory quality system.
Requires: Candidates must have at minimum a Bachelor's degree in science ( e.g. chemistry, biology, biochemistry, etc.), and at least 1-3 years regulated documentation experience in the pharmaceutical industry. Candidates must have excellent written and verbal communication skills, must be conversant with current Good Manufacturing and Laboratory Practices (cGMP/cGLP), and must be familiar with the latest USP, ICH and FDA regulatory guidelines. Must be computer literate in Word, Excel and database programs. The position requires the ability to manage multiple projects, meet critical deadlines, and work in a team-oriented environment.
|