Description
Quality Control (QC) Analyst IIA pharmaceutical company in the South San Francisco area is looking for a Quality Control (QC) Analyst II to join their team. This an excellent opportunity to join a team with a stead pipeline and promising growth.
Quality Contrl (QC) Analyst II Responsibilities:
- Perform testing of routine and non-routine samples and document according to GMP.
- Review data and assess against established acceptance criteria
- Perform technical review of peer-generated data for basic methods
- Prepare data tables and graphs
- Identify discrepancies, participate in quality investigations and CAPA (corrective actions preventive actions) initiatives as needed.
- Receive and provide training
- Participate in assay transfer and assay validation.
- Perform equipment qualification / maintenance
- Prepare and maintain standards, controls, stocks, and cultures per established procedures
- Support the maintenance and compliance of operational areas.
- Assure and apply GMP throughout operations.
- Coordinate with customers to support operational activities.
- Support internal and external audits.
- Work to meet schedules.
- Identify and support resolution of technical problems.
- Actively participate in group and project teamwork; project and process improvements.
- Drafts protocols and reports under supervision.
- Meets scheduled performance of 95% on time.
- Perform other duties as requested by managers to support Quality activities.
- Position may involve use of reagents and other chemical compounds, including but not limited to acetonitrile, chlorine, acids and bases, biologic toxins, microorganisms and potent compounds.
Quality Control (QC) Analyst II Requirements:
- B.S./B.A. degree (preferably in relevant scientific discipline) or an equivalent combination of education and experience.
- Ability to write clearly and effectively and have good verbal communication skills
- Basic knowledge of scientific theories, principles and techniques used in analytical or biological test procedures.
- Ability to exercise sound judgment, reasoning and problem solving.
- Capable of completing assigned responsibilities and keeping manager informed of status
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Basic understanding of the analytical techniques cited above helpful. Computer literacy and experience working in a cGMP lab environment preferred.
If you are interested in applying to this position, please respond to this job posting ASAP with an updated version of your resume.
To find out more about Real Staffing please visit www.realstaffing.com