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This position is part of Genentech’s’ Pharma Technical - individualized and cell therapy team based in Hillsboro, Oregon. In this critical role, you will be part of a dedicated cross-functional team working on production start-up activities including building GMP-compliant processes to manufacture, test and release products in a fully GMP-compliant facility, and the quality approach for this exciting and novel technology.

The Opportunity :

In this role, you will be responsible for ensuring that both commercial and clinical (IMP) products meet specified requirements and are released in accordance with legal compliance and Roche quality standards. Your primary accountability will encompass reviewing and approving QA controlled documentation, including procedures and master batch records. Additionally, you will :

Ensure lot disposition and timely release of commercial and clinical products in compliance with internal standards and local / international laws

Create, revise, and review quality documents; provide oversight for operational procedures to maintain GMP compliance

Lead and support cross-functional projects and Quality initiatives; resolve Quality risks through interdepartmental collaboration

Assess and resolve deviations promptly, partnering with functional areas to investigate and address product quality impacts; manage CAPA processes effectively

Meet budgetary goals for QA Operations and promote a positive safety culture aligned with Safety, Health and Environment requirements

Provide Quality Assurance oversight of end-to-end production operations, including Chain of Custody and Chain of Identity

Participate in internal and external audits as a Subject Matter Expert, ensuring readiness for inspections and defending lot disposition practices and GMP compliance

Collaborate with Manufacturing, Site functions, PTD, Affiliate Quality Assurance Management, Regulatory (PTR), Global Quality System and Management, External Quality, Supplier Quality, suppliers, and CMOs to ensure cohesive quality standards and compliance across all operations

Please note : We offer the opportunity to join our team at either the QA Specialist III or QA Senior Specialist level, depending on your experience and qualifications.

Qualifications for QA Specialist III :

You possess a Bachelor's Degree (preferably in Pharmacy, Pharmaceutical, bioengineering, Chemistry or other relevant discipline) AND at least 3 years of pharmaceutical or related life science industry experience

You possess at least 3 years of experience in Quality Assurance, Quality Control, Manufacturing

You possess knowledge of Quality Assurance principles, practices, and standards for the biopharmaceutical industry

You have an understanding of GMP relevant to the pharmaceutical industry and knowledge of local and international GMP regulations; knowledge of regulations related to ATMP is desirable

You possess strong verbal and technical written communication skills, excellent interpersonal skills, and negotiation skills

You are an effective problem-solver

You are familiar with computer systems and aptitude to quickly become familiar with new software (e.g., EDMS, LIMS, SAP)

Qualifications for Senior QA Specialist :

You possess a Bachelor's Degree (preferably in Pharmacy, Pharmaceutical, bioengineering, Chemistry or other relevant discipline) AND 6 or more years work experience in the pharmaceutical or related life science industry

You possess at least 8 years of experience in Quality Assurance, Quality Control, Manufacturing

You possess expert knowledge of Quality Assurance principles, practices, and standards for the biopharmaceutical industry

You have an expert understanding of GMP relevant to the pharmaceutical industry and knowledge of local and international GMP regulations; knowledge of regulations related to ATMP is desirable

You possess excellent verbal and technical written communication skills, excellent interpersonal skills, and negotiation skills

You demonstrate excellent problem-solving skills, tactical strategy, and diplomacy

You have demonstrated experience with computer systems and aptitude to quickly become familiar with new software (e.g., EDMS, LIMS, SAP)

Compensation :

The expected salary range for the Quality Assurance Specialist III in Oregon is $77,500 - $110,700 (mid) - $143,900 (max). For the Senior Quality Assurance Specialist, the salary range is $94,010 - $134,300 (mid) - $174,590. 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.

Notes :

Relocation benefits are approved for this position.

This position is an on-site role; remote options are not available.

The ability to work flexibly outside of normal business hours may be required to support business operations.

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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.

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