Senior Validation EngineerNorthbridge

Senior Validation EngineerNorthbridge Employer EyePoint Location Northbridge Start date May 11, 2026 View more categories View less categories Discipline Engineering , Manufacturing & Production , Operations , Process , Science/R D , Biotechnology Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details The Senior Validation Engineer is responsible for providing technical leadership and execution support for validation activities required to achieve and maintain regulatory compliance in preparation for an NDA filing and commercial readiness. This role oversees validation efforts across process validation (PV), Process Performance Qualification (PPQ), facility and utility qualification, equipment qualification, computer system validation (CSV), automation/controls validation, and validation lifecycle management . The Senior Validation Engineer ensures that all validation deliverables meet applicable regulatory requirements, internal quality standards, and inspection‑readiness expectations. This position is based at our Northbridge, MA facility. We offer a hybrid work schedule. Essential Duties and Responsibilities Lead the development, execution, and approval of Process Validation and PPQ protocols and reports , ensuring alignment with FDA, EMA, and ICH guidelines. Support the establishment and maintenance of a robust process control strategy and contribute to Continued Process Verification (CPV) planning. Plan, execute, and document facility, equipment, and utilities qualification activities, including IQ/OQ/PQ, in accordance with internal procedures and regulatory expectations. Lead and support Computer System Validation (CSV) activities following GAMP 5 and 21 CFR Part 11 requirements, including validation of automation and control systems. Ensure validation documentation is maintained in a state of inspection readiness , supporting internal audits, regulatory inspections, and pre‑approval inspection (PAI) preparation. Conduct validation lifecycle gap assessments , develop remediation plans, and drive closure of identified gaps. Contribute to the development, revision, and implementation of Validation Master Plans (VMPs), validation SOPs, risk assessments, and related quality system documentation . Collaborate cross‑functionally with Manufacturing, Quality Assurance, Engineering, MS&T, and Regulatory Affairs to ensure validation activities support operational and regulatory objectives. Provide subject matter expertise (SME) during audits, inspections, and technical discussions. Mentor junior validation staff and support training initiatives related to validation practices and compliance requirements. Education Requirements Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related technical discipline required. Experience Requirements Minimum 8-12 years of validation experience in the pharmaceutical, biotechnology, or related regulated industry. Demonstrated experience leading process validation and PPQ activities in support of NDA/BLA submissions or commercial product launches. Strong background in facility, equipment, and utilities qualification , including cleanroom environments and critical utilities (e.g., compressed gases, WFI, etc.). Hands‑on experience with CSV and automation validation , including PLC, SCADA, HMI, and data integrity compliance. Proven experience supporting regulatory inspections , including PAI preparation and response. Familiarity with applicable regulations and guidance, including

FDA, EMA, ICH Q7/Q8/Q9/Q10/Q12, EU

Annex 15, and data integrity principles . Knowledge, Skills, and Abilities Strong understanding of validation principles, risk‑based approaches, and lifecycle management. Proficiency in technical writing, protocol development, and documentation review. Ability to interpret and apply regulatory requirements to validation strategies. Strong analytical and problem‑solving skills, including experience with statistical tools and process capability concepts. Excellent communication, organizational, and cross‑functional collaboration skills. Demonstrated leadership capability and ability to mentor junior staff. Ability to work independently in a fast‑paced, evolving environment. Working Conditions Standard office and GMP manufacturing/cleanroom environments. Some travel may be required for vendor visits, FAT/SAT activities, or corporate meetings. EyePoint is committed to fair and equitable compensation practices. The salary offer is commensurate with EyePoint's compensation philosophy and considers factors including but not limited to education, training, experience, market conditions, criticality of the role and internal equity. The target salary range for this position is listed below: Salary Range $128,750 - $163,083 USD Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Company EyePoint is a specialty biopharmaceutical company committed to developing and commercializing innovative ophthalmic products in indications with high unmet medical need to help improve the lives of patients with serious eye disorders.

Company info Website http:

//www.eyepointpharma.com/ Location 480 Pleasant Street Suite B300 Watertown Massachusetts 02472 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Process Engineer (Fill-Finish) Swiftwater, Pennsylvania GMP Utility Engineer Worcester, MA Sr. Process Engineer Remote