Senior Validation Engineer

AstraZeneca • Redwood City, CA

1d • $101,643 - $152,465 • Onsite

About The Position

The role is heavily focused on supporting the key site digital/software/automation transformation and related validation activities. The first two years will focus on validation of digital tools (MES systems, software, etc.) and may require continued administrative support of these systems. The position is responsible for performing adequate and comprehensive qualification and validation of equipment, processes, products, and facilities at the Redwood City site to support site goals and targets. This includes assuring the design, installation, implementation, data integrity, and validation of computer systems meet all applicable industry standards and regulatory requirements. The role may also serve as a system or business owner, overseeing the system from implementation and ensuring proper documentation at every phase.

Requirements

• Entry-level Master’s/ PhD degree in engineering, science, technology, or related field (OR) Bachelor’s degree with 3+ years of relevant experience.
• At least 3 years’ experience in independent development, writing and performance qualifications / validation.
• Experience in and knowledge of qualification of control systems and computer system validation.
• Proven capability to assess processes, equipment and products for sources of variation.
• Ability to analyze data and reach appropriate solutions.
• Ability to perform and appropriately document deviations and investigations.
• Excellent analytical skills and attention to detail.
• Work requires a high degree of accuracy in complex documentation.
• Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and validations.
• Must have the ability to learn technical subject matter quickly and integrate knowledge into previously known information.
• Must effectively evaluate information collected from various sources and determine impact upon controlled state of processes, equipment, facilities, and products.
• Must be goal oriented and quickly adaptable to new situations.
• Excellent technical writing and verbal communication skills.
• Experience with Process Engineering or setting up new equipment– (URS, PID, DQ, IQ, OQ, PQ).
• Experience working with digital tools and applications related to reporting, documentation, and analysis.

Nice To Haves

• Ability to read P&IDs and electrical drawings.
• Working knowledge of FDA guidance on Process Validation and Computer System validation.
• Experience with various programming to support digital/software validation.
• Knowledge of hardware and/or software integration.

Responsibilities

• Support implementation of the Site Digital Technology Strategy and roadmap, architecting key strategic digital transformation initiatives aligned to business priorities and value targets.
• Develop and lead CSV and Life-cycle management activities to support GxP conforming systems, facilities, manufacturing, and laboratory systems.
• Evaluate equipment and processes to identify critical parameters based upon potential impact on product quality attributes.
• Prepare qualification, requalification, and process validation protocols, analyze applicable data, and prepare final reports in compliance with relevant regulations, industry practices, and AZ policies and procedures.
• Perform and document field verification of equipment, instruments, and facilities as required by approved protocols.
• Assess accuracy of P&ID, Electrical drawing to support validation and change control.
• Provide supervision and training for less experienced or entry-level validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages.
• Provide supervision and training for contract validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages.
• Perform risk assessment on proposed changes, document change control deliverables with respect to validation requirements.
• Complete, review, and/or approve risk assessments for instruments, equipment, processes, and products.
• Analyze data and information to determine whether processes, equipment, and products are within an appropriate state of control during qualification and validation, as well as in assessing the need for requalification/revalidation on a periodic basis.
• Prepare and/or evaluate change controls to ensure that equipment, products, processes, and facilities remain in a qualified, validated state, including definition of appropriate requirements in change control documents, completion of identified actions, and preparation of applicable reports and data packages.
• Identify and investigate unusual or unexpected events, data, or sources of variation during the development and performance of qualifications/validations; assess and document the impact upon qualification or validation as applicable, and recommend appropriate corrective/preventive actions.
• Coordinate assigned qualification projects as needed with other departments.
• Ensure that work is performed in accordance with applicable regulations, industry guidelines and practices, approved procedures and cGMP.
• Other responsibilities as assigned by department management.

Benefits

• Qualified retirement programs
• Paid time off (i.e., vacation, holiday, and leaves)
• Health coverage
• Dental coverage
• Vision coverage
• Eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level