Genentech
Quality Control Associate
Genentech - San Francisco, California, United States, 94199
Work at Genentech
Overview
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Overview
The Position
In Pharma Technical Development (PTD), we actively collaborate and develop creative technical solutions to efficiently transform scientific ideas into products. Our mission is to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, teamwork, dedication and mutual respect, and contributes every single day, continuously improving what it does. Global Analytical Development and Quality Control (ADQC) organization is a leader in developing, validating, and executing physico-chemical, immunochemical, and biological methods for our biologics pipeline. This function provides integrated analytical control strategies and systems that enable CMC development of biologic therapeutics, process development, product characterization, and drug delivery for biologic products from research (molecular assessment) through post product launch. The Opportunity
We have a great opportunity to join our team as a lab analyst performing physico-chemical testing of biologics and other pharmaceutical compounds, along with general lab operations. Previous GMP experience in a biopharmaceutics environment is preferred. The role will be responsible for performing analytical, biochemical, and/or biological testing; data review; and/or related activities that support QC operations. Responsibilities: Perform a broad variety of basic and moderately complex tests with documentation according to GMP
Maintain accountability for deliverables affecting department and organizational objectives
Maintain a state of inspection readiness
Identify discrepancies and support resolution of technical problems
Supports department to meet corporate goals and department objectives
Perform any other tasks as requested by Management to support Quality activities
Actively participate in group and project teamwork
Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area.
Perform physico-chemical testing for biologics and other pharmaceutical compounds.
Schedule and Perform routine and semi-routine assignments and support lab maintenance operations.
Adhere to cGMP policies and procedures, including documentation of activities
Record information and complete transactions in applicable cGMP systems
Coordinate with customers to support operational activities
Who you are
The successful candidate will possess the following skills and experience: Bachelor's degree, preferably in a scientific discipline, or Associate's degree with 5 years of related experience preferably in a bio-pharmaceutical cGMPgmp lab environment
QC / cGMP
experience working in a lab environment in an industry or academic setting is strongly preferred
Ability to communicate clearly and effectively, both verbally and in writing
Ability to exercise sound judgment, reasoning, and problem-solving capabilities
Attention to detail with strong organization and prioritization skills
Takes accountability and works effectively as part of a team
Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of South San Francisco, CA is $78,500 to $145,900. 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 . Benefits Genentech 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 .
#J-18808-Ljbffr
In Pharma Technical Development (PTD), we actively collaborate and develop creative technical solutions to efficiently transform scientific ideas into products. Our mission is to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, teamwork, dedication and mutual respect, and contributes every single day, continuously improving what it does. Global Analytical Development and Quality Control (ADQC) organization is a leader in developing, validating, and executing physico-chemical, immunochemical, and biological methods for our biologics pipeline. This function provides integrated analytical control strategies and systems that enable CMC development of biologic therapeutics, process development, product characterization, and drug delivery for biologic products from research (molecular assessment) through post product launch. The Opportunity
We have a great opportunity to join our team as a lab analyst performing physico-chemical testing of biologics and other pharmaceutical compounds, along with general lab operations. Previous GMP experience in a biopharmaceutics environment is preferred. The role will be responsible for performing analytical, biochemical, and/or biological testing; data review; and/or related activities that support QC operations. Responsibilities: Perform a broad variety of basic and moderately complex tests with documentation according to GMP
Maintain accountability for deliverables affecting department and organizational objectives
Maintain a state of inspection readiness
Identify discrepancies and support resolution of technical problems
Supports department to meet corporate goals and department objectives
Perform any other tasks as requested by Management to support Quality activities
Actively participate in group and project teamwork
Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area.
Perform physico-chemical testing for biologics and other pharmaceutical compounds.
Schedule and Perform routine and semi-routine assignments and support lab maintenance operations.
Adhere to cGMP policies and procedures, including documentation of activities
Record information and complete transactions in applicable cGMP systems
Coordinate with customers to support operational activities
Who you are
The successful candidate will possess the following skills and experience: Bachelor's degree, preferably in a scientific discipline, or Associate's degree with 5 years of related experience preferably in a bio-pharmaceutical cGMPgmp lab environment
QC / cGMP
experience working in a lab environment in an industry or academic setting is strongly preferred
Ability to communicate clearly and effectively, both verbally and in writing
Ability to exercise sound judgment, reasoning, and problem-solving capabilities
Attention to detail with strong organization and prioritization skills
Takes accountability and works effectively as part of a team
Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of South San Francisco, CA is $78,500 to $145,900. 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 . Benefits Genentech 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 .
#J-18808-Ljbffr