Senior Validation Engineer II, III

We are seeking a Senior Validation Engineer with solid hands‑on validation experience and a collaborative mindset to help drive validation harmonization across the Cellares global landscape. The primary focus of this position will be responsible for execution activities for QC and Manufacturing equipment. In addition to many of the equipment seen at traditional cell & gene therapy facilities, this position will focus on the qualification and validation of several Cellares proprietary equipment.

The ideal candidate will have a deep understanding of qualification and validation lifecycle activities across all manufacturing process streams, and the ability to apply that knowledge base to the Cellares Cell Shuttle and Cell Q. In addition to equipment qualification and validation, the person in this position will also execute facilities and utility systems. The desired candidate will be very hands‑on with execution, but also develop documentation;

validation/qualification protocols (IQ/OQ/PQ), risk assessments, system impact assessments, summary reports, SOPs and other technical documents. This position, at times, will require the oversight of contract workers, junior level engineers and equipment vendors.

Candidates should enjoy working in a fast‑paced, mission‑driven environment, be comfortable with justified risk‑based approaches, and be prepared to tackle a broad selection of challenges as the company grows.

• Generate and develop qualification and validation lifecycle documents, templates, protocols, reports including but not limited to SOPs related to the commissioning, qualification and validation programs, risk assessments, system impact assessments, validation master plans, URS, project plans, validation master lists
• Review validation protocols, executed validation studies, and validation summary reports as needed to support GMP manufacturing and laboratory systems
• Ensure maintenance of validated status via periodic review (PR) and requalification activities
• Knowledge of CSV methodology and required lifecycle document content including risk‑based approaches used to validate technical systems
• Knowledge of data integrity and ALCOA+ principles and the applicability to process and analytical systems
• Knowledge of QC equipment validation as it relates to the interface of IQ/OQ and method validation
• Support vendor qualification activities including risk assessments and participate in the selection of vendors that support validation effort
• Support the change control program with respect to facility, equipment, and utility validation changes. Evaluate validation impact of equipment introduction/upgrades and software/hardware changes
• Follow written SOPs, and ensure SOP training remains current
• Oversee contractors who carry out commissioning, qualification and validation projects related to facility, utility, and equipment
• Provide guidance on topics to foster a quality culture and quality mindset
• Actively participate in continuous improvement activities with cross‑functional teams
• Provide status updates to stakeholders and internal customers of validation activities in their respective areas
• Identify qualification/validation gaps, strategize on solutions, drive gap mitigation
• Mentor and train junior level engineers
• Foster a collaborative approach to ensure harmonization of qualification/validation approach across all Cellares sites
• Participate in regulatory inspections

• Minimum of a Bachelor’s degree in Engineering or a scientific related field and 8 years of experience working in a GMP regulated environment
• Minimum of 5 years qualification and validation hands‑on experience
• Detailed knowledge of 21 CFR Part 210, 211, Device GMPs (21 CFR Part 820), EU GMPs (Annex
  1) requirements
• Knowledge of System Development Life Cycle concepts and software (GAMP5 expected pharmaceutical standards, 21 CFR Part 11)
• Excellent technical writing skills with an understanding of good documentation practice
• Self‑motivated, detail‑oriented and passionate about advancing the field of cell therapies
• Collaborative, solution‑oriented, comfortable in an agile environment

$90,000 - $210,000 a year

Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.