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Sr Qc Analyst

Company: GENENTECH
Location: Oceanside
Posted on: January 12, 2021

Job Description:

The Position Summary:Conduct routine and non-routine analysis of manufactured in-process commercial products according to standard operating procedures. Responsible for collecting, processing and reporting of data. Prepares reagents and maintains laboratory in an audit ready and cGMP compliant manner at all times. Review and evaluate own data for conformance to specifications and assist with investigation of laboratory deviations. Revise and update standard operation procedures. Display good manufacturing practices and good laboratory practices on a daily basis. Ensure quality and safety of manufactured products. Work independently with little supervision. Assist with investigations and data review related to area of expertise. Use state-of-the-art techniques to evaluate and implement new techniques and technologies. Essential:Proficient in cGMP practices in all aspects of laboratory assignments Collect, process and report on data for samples associated with environmental monitoring and in-process testing from the commercial manufacturing facilities Apply basic and advanced troubleshooting methods Initiate, compile, and perform lab investigations that include reviewing documents, conducting internal and external interviews, and tracking information Perform microbiological and chemical assays at all levels of complexity to support manufactured products Serve as subject mater expert for an assigned assay Train others in basic to complex laboratory and troubleshooting techniques Evaluate and implement new techniques and technologies Responsible for working with a team of analysts to perform analytical testing of samples Assist in data trending, data review, and lab maintenance Participate in non-routine projects Apply knowledge to assist in investigations and support studies and protocols Responsible for collecting, entering data and generating reports from electronic systems Peer review of data relating to analysts area of expertise All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Supplementary Responsibilities:Attend team, department and corporate meetings as required Attend seminars and/or classes necessary to support business demands ? Requirements:Education and Experience:BS/BA in Microbiology, Biochemistry, or related Science 3 years related experience Knowledge, Skills, and Abilities:Demonstrate excellent organizational skills Ability to read and follow Standard Operating Procedures Excellent interpersonal, written and verbal communication skills Must have working knowledge in manual and automated chemical and microbiological assays Must be able work independently as well as within a team in a fast pace environmental Work Environment/Physical Demands/Safety Considerations :Work in office and laboratory environment Ability to stand for 8 to 10 hours a day Ability to lift up to 30lbs Ability to climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility May work in the clean room environment that requires gowning and no make up or jewelry May work in the clean room environment which can be a loud environment from 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 Available to work over-time, weekends, and holidays as needed #LI-CA1 #ptcareers Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. Diversity and Inclusion (D&I) are critical to the success of our company and our impact on society. We believe that by championing diversity of background, thought and experience, we can foster a sense of belonging and provide an environment where every employee feels valued, included, and able to contribute their best for the patients we serve. We're focused on attracting, retaining, developing and advancing our people to their full potential by rewarding bold ways of thinking and integrating inclusive behaviors into every aspect of our work. The next step is yours. To apply today, click on the "Apply for this job" button. Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page . Job Facts JOB FUNCTION Quality Control COMPANY/DIVISION Pharmaceuticals SCHEDULE Full time JOB TYPE Regular

Keywords: GENENTECH, Oceanside , Sr Qc Analyst, Professions , Oceanside, California

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