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Job Requirements of Scientist:
-
Employment Type:
Contractor
-
Location:
Collegeville, PA (Onsite)
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Scientist
Careers Integrated Resources Inc
Collegeville, PA (Onsite)
Contractor
Job Title: Scientist
Location: Collegeville, PA
Duration: 9 Months+
Job Description: Summarized Purpose:
Location: Collegeville, PA
Duration: 9 Months+
Job Description: Summarized Purpose:
- Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence.
- Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices.
- Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison aProductst SOP acceptance criteria, methodology, protocol and product specifications.
- Enters data into databases and reports. Performs self review for own data prior to QC submission.
- Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and /or biological matrices for stability and analytical testing.
- Works with multiple functional groups to meet business needs.
- Plans and organizes work with periodic supervision.
- Sets up and maintains analytical instrumentation.
- Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
- Ensures QA findings are addressed appropriately.
- Provides assistance and training to other team members.
- Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems.
- Communicates project status to project leader.
- Performs work assignments accurately, and in a timely and safe manner.
- Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
- Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Demonstrated knowledge of multiple applicable techniques such as: HPLC, GC, MS, Dissolution Testing, Inhalation Testing, Biopharmaceutical Testing, Karl Fischer, UV-Vis, FT-IR, TOC
- Proficient in Microsoft Excel and Word
- Proven ability to interpret data by performing trend analysis
- Proven ability in technical writing skills
- Ability to independently optimize analytical methods
- Proven problem solving and troubleshooting abilities
- Good written and oral communication skills
- Time management and project management skills
- Ability to work in a collaborative work environment with a team
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