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QC Technician II and Technical Services Representative (Sorrento Valley)
By | July 14, 2010
Invivoscribe Technologies, Inc., is a privately-held corporation dedicated to improving the quality of healthcare worldwide by providing high quality, reliable, cutting-edge tools for molecular research, molecular diagnostics, and personalized molecular medicine.
Invivoscribe provides a comprehensive selection of PCR-based gene rearrangement, chromosome translocation, and gene mutation Research Use Only testing reagents and controls. We also provide CE-marked in vitro diagnostic products to customers outside North America, and our subsidiary, LabPMM, provides comprehensive international access to clinical testing of patient samples. Customers include many of the world’s leading pharmaceutical and biotechnology companies, medical centers, cancer research centers, reference laboratories and molecular testing centers.
We have an immediate opening for a Full-Time QC Technician II and Technical Services Representative (QCTII).
Duties and Responsibilities include the following:
Responsible for assuring that only quality products are released for distribution. It is their job to ensure that products are tested to meet the applicable government regulations and industry standards
Responsible for resolving customer inquiries and complaints.
Effectively maintain and improve the Standard Operating Procedures (SOP), acceptance criteria, etc. for the department and products tested.
Effectively and efficiently test raw materials, in process and final product and generate testing data.
Releases products to QA for final approval.
Ensure that all customer complaints and inquiries are resolved.
Conduct and maintain the real time stability study testing.
Maintain inventory materials used in quality control.
Requirements:
Requires knowledge and skills normally acquired through the successful completion of a BS Degree in a scientific discipline.
Requires 1+ years of experience in a GMP regulated industry or equivalent combination of education and experience.
Direct working knowledge of a production environment, including use of SOPs, batch records, ERP systems and purchasing specifications.
Direct working knowledge of PCR (polymerase chain reactions), gel electrophoresis, capillary electrophoresis, DNA/RNA isolation and purification, and cDNA synthesis.
Strong working knowledge molecular biology.
Ability to recognize deviation from accepted practice is required.
Experience with sterile techniques and accurate pipetting skills.
Meticulous and detailed oriented.
Ability to follow Standardized Operating Procedures (SOPs) as well as written and verbal instructions.
Ability to work independently as well as in a team environment.
Excellent written and verbal communication skills with the ability to train employees.
Ability to manage multiple projects and changing priorities.
Willingness to learn and take on new challenges.
Able to use Adobe Acrobat, Illustrator, and Photoshop for artwork and graphics in documents.
Ability to perform some tasks that are monotonous & physically demanding in lab environment. Repetitive pipetting, labeling, and capping/uncapping tubes are required.
Some activities will take place at a desk and on a computer.
PLEASE SPECIFY THE POSITION AND APPLY IN ONE OF THE FOLLOWING WAYS:
Submit your resume via email at HR5@invivoscribe.com.
Fax: 858-623-8109
Please be sure to reference Job Code: KSMT in the subject line of either your cover letter or email to be considered for this position.
Please, no phone calls about this position.
Please, no walk-ins inquiring about this position.
COMPENSATION:
Competitive salary that is commensurate with experience.
IVS provides health, dental, and vision coverage and a 401(k) retirement plan.
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