QC Scientist II Job

QC SCIENTIST II needed for a CONTRACT opportunity with Yoh's client located in MELVILLE, NY.

THE BIG PICTURE - TOP SKILLS SHOULD YOU POSSESS:

- Pharmaceutical
- Method Development/Validation

WHAT YOU'LL BE DOING:

- Responsible for the independent management of assigned projects. This includes the evaluation, development and validation of methods required for raw materials and finished products. Conducts research to develop or improve analytical techniques, methodology, procedures and investigates application of instruments in analysis.
- Performs qualitative and quantitative analyses of organic and inorganic compounds to determine the identity, purity and homogeneity of drug substances and products related to each project.
- Organizes and interprets all data obtained using a wide variety of instrumental technologies.
- Evaluates new technologies for application to the current and future business needs.
- Implements QC specifications to ensure process consistency, quality and optimal performance.
- Ascertains relationships between molecular structure and physical properties to aid in the analysis of compounds.
- Responsible for understanding the Change Control system and the requirements for submitting validation reports and protocols so as to fully implement method requirements and specifications.
- Assessment and Establishment of Product Expiry Dating.
- Seeks out opportunities to evaluate technologies applicable to Quality Control testing.
- Trains new team members.
- Pursues subject matter expert status for a specific technology or testing discipline.
- Develops analytical methods for full range of testing in both Raw Materials and Finished Products. Selects appropriate methodologies, technology and techniques for those methods to be validated.
- Writes and reviews validation protocols and reports. Adept at instrumentation troubleshooting.
- Works with customers in QC Supply Chain, Quality Assurance, Regulatory Affairs and Technical Services to ensure the customer needs are understood and met.
- Ensures all company policies and procedures are adhered to.
- Conducts self in a manner consistent with Novartis Behaviors and supports Quality Culture initiatives.
- Performs other duties as assigned
- Adheres to all applicable procedures, cGMP's, company policies, and all other quality or regulatory requirements (OSHA, DEA, FDA, HS&E, and USP/NF etc.).
- Ensures all work is performed in a safe, effective manner, and in compliance with the appropriate industry and regulatory standards, and Departmental, Plant, and Corporate quality and Behavioral Based Safety (BBS) goals.

WHAT YOU NEED TO BRING TO THE TABLE:

- Minimum fifteen (15) years of Pharmaceutical method development/validation experience with PhD required.
- BS or MS with significant method development/validation experience in a pharmaceutical environment will be considered only in exceptional cases.

OPPORTUNITY IS CALLING, APPLY NOW!

RECRUITER: Hannah Cihlar

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

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