Manager, QA Operations

The Manager, Quality Assurance (QA) Operations ensures compliance with the quality system's procedures and assesses regulatory and quality risks in activities and processes according to regulatory agency guidelines and company practices. This role is accountable for routine Quality Assurance duties related to the production and disposition of products manufactured and tested on behalf of Neogene. This role is based in Santa Monica, CA, and reports to the Director of Quality.

What you will do:

• Provide quality assurance support across departments (Manufacturing, Supply Chain, QC, Process Development, Regulatory Affairs) within Neogene and externally to assure compliance and relationships.

• Perform several activities to ensure compliance with applicable quality goals and regulatory requirements.

• Batch documentation ensures resolution of issues to release product.

• Approval of Deviations and CAPAs Support the Disposition of products for the U.S. and other countries.

• Support New Product Introductions.

• Support quality assessments of internal operations to analyze quality compliance and assess risk.

• Provide QA guidance on product development projects and technical transfer activities

• Support Management Review activities and oversee trending of important quality, product, and GMP metrics.

• Support regulatory inspections, internal audits, and external audits from partners.

• Develop QA Standard Operating Procedures to ensure Quality goals are met

• Review routine manufacturing and quality control data for in-process and finished product.

• Develop solutions to more complex problems.

• May conduct or serve as a lead/coordinator of investigations and corrective and preventive action (CAPA) recommendations related to manufactured products.

Minimum Qualifications:

• Bachelor's degree with a minimum of 7 years of experience OR Master's Degree and a minimum of 5 years of experience OR PhD with a minimum of two(2) years experience in a GMP environment.

• Knowledge of and ability to apply GMP in conformance to US, EU, and ROW standards.

• Proficient in cGMP regulations, quality systems, and regulatory requirements.

• Experience writing, evaluating, and closing investigations, CAPAs and change control records.

• Experience conducting internal and external audits.

• Experience supporting Quality Control Analytical and Facilities & Engineering teams.

• Will to accept temporary responsibilities outside of the initial job description.

• Ability to build collaboration amongst individuals.

• Proficient in MS Word, Excel, PowerPoint, and other applications.

• Willingness to think outside of the box and adapt best practices for stage-appropriate products.

• Demonstrate organizational, prioritization, and proficiency.

When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

The annual base salary for this position ranges from $95,446 to $143,170. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Date Posted

03-Dec-2024

Closing Date

30-Dec-2024Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.