Sr. QC Associate - Direct Material

We are seeking for an experienced Sr. QC Associate Direct Material (raw material) to support direct material validation and testing.  In this role the associate will apply knowledge of good manufacturing practices and good laboratory practices on a daily basis. Calibrate and maintain laboratory and instrumentation equipment. Revise and update standard operation procedures. Develop and/or optimize testing methods and troubleshoot testing methods. Maintain laboratories in audit ready and cGMP compliant manner and participate in audits. Compile data for documentation of test procedures and prepare reports for internal and regulatory submissions. Review and evaluate data for conformance to specifications/reports. Investigate anomalous data. Use state-of-the-art techniques to evaluate and implement new techniques and technologies. Maintain validation program for QC laboratory analytical instruments. Evaluate and trend data and discrepancies. Provide ongoing training and process improvements. Lead product operations with special projects. Support audits as a subject matter expert.  The OpportunityValidation & Documentation Leadership – Creates, reviews, and approves validation documents while providing process and equipment knowledge, training, and day-to-day support to QC partnersOperations & Problem Resolution – Monitors equipment and processes to identify and resolve issues, troubleshoots complex assay and equipment problems using advanced techniques, and identifies functional improvementsLaboratory Testing & Analysis – Performs microbiological and chemical testing at all complexity levels, conducts lab investigations, manages environmental monitoring data, and evaluates new techniques and technologiesTechnical Expertise & Training – Serves as a subject matter expert and liaison across departments, trains analysts in basic to complex laboratory techniques, provides professional guidance, and represents QC during auditsSafety, Compliance & Data Management – Ensures safety and security compliance (including TSA requirements where applicable), collects and generates data reports from electronic systems, and fosters a positive safety culture.Supplementary Responsibilities Act as supervisor designee in cross-site and/or interdepartmental meetings Facilitate team meetings as required Attend department meetings as required Who you areYou possess a Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemistry or other relevant discipline with 7-8 years of related experience.Knowledge, Skills, and Abilities Demonstrate excellent organizational skills Strong written and verbal communication skills, with demonstrated leadership in a large group Computer skills- LIMS, Microsoft Word, Excel, Power Point, Visio Ability to read and follow Standard Operating ProceduresWork under limited direction and guidance Ability to invest time, as required, to expedite or complete assignments or projects. This shall include working non-standard hours such as evenings and weekends as necessary. Demonstrate strong spreadsheet, word processing and database skills necessary to process and present technical data in a clear and concise manner. Ability to read, interpret, and troubleshoot technical data Ability to use discretion and good judgment in making decisions including the ability to know when to refer a problem to senior level staff. Demonstrate excellent written and verbal communication skills Demonstrate strong presentation skills including the ability to prepare and deliver professional presentations to external business interests. Ability to work in a fast pace environment with high volume testing schedules Experience in chemical testing assays Experience with electronic systems used in laboratories Ability to multitask and manage time effectively Knowledge of laboratory safety procedures Experience working in GMP environment Experience speaking to auditors Work Environment/Physical Demands/Safety ConsiderationsWork in office and laboratory environment Lift up to 30lbs May work in the clean room environment that requires gowning and no make up or jewelry May work in the clean room environment where it is loud due to different equipment operating Work with some hazardous materials and chemicals Ability to sit, stand and move within work space for extended periods Ability to perform repetitive tasks including frequent hand to finger manipulations, grasping pushing and pulling. Ability to stand 8 to 10 hours a day. May be required to work some evenings and weekends Travel may be up to 25% during start-up laboratory activities.   No more than 10% travel expected during routine operations.   Relocation benefits are not available for this posting.The expected salary range for this position based on the primary location of California is $68,300.00 - $110,000.00 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.BenefitsGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.