Validation Engineer II

Job Description Perform start-up, commissioning, qualification, validation and revalidation for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, medical device, and drug product manufacturing processes. Strategic Focus Area: Develops into a subject matter expert in process validation and cleaning/sterilization validation. Specific Responsibilities: * Authors, executes, and summarizes qualification and validation protocols. * Conducts Risk / Impact Assessments and establishes system boundaries. * Ensures protocols, records, and procedures are in compliance with current Good Manufacturing Practices (cGMP), industry standards and approved SOPs. * Provides technical input in determining strategy for validation activities. * Represents validation during site GMP activities and participates on cross-functional teams. * Coordinates the investigation and impact assessment for all deviated equipment or processes discovered upon calibration or validation. * Initiates, or provides validation input on quality systems such as CAPAs and change controls. * Responsible for other duties and projects as assigned. Job Complexity: The job requires the ability to work on diverse complex issues where analysis of situations or data requires an in-depth evaluation of a variety of factors. The position exercises broad judgment in selecting optimum methods, techniques, and evaluation criteria for obtaining results. Supervisor Responsibilities: None Experience, Knowledge and Skills Required: * BS degree in engineering or scientific discipline or equivalent experience. * 3-5 years of validation experience in pharmaceutical, medical device or FDA regulated environments. * Strong understanding of cGMP and regulations related to facility, utility, equipment, and process validations. * Ability to initiate, manage and close quality systems such as change control, CAPA and deviation management. * Detailed experience performing root cause analysis investigations for deviations and non-conformances having technical scope. * Excellent written and verbal communications skills. Desired Experience, Knowledge, and Skills: * Advanced degree or post-graduate coursework may be desirable. * Hands on experience on process validation of medical device and/or drug product manufacturing processes. * Knowledge of the fundamentals of Steam Sterilization and Cleaning Validation. * Solid understanding of quality risk management principles and statistical concepts as applicable to area of responsibility. * Subject matter expert on regulations and best practices pertaining to validation. * Practical application and knowledge of ISO 13485, GHTF Process Validation Guidance and other applicable standards used in the medical device manufacturing. The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law. We are an equal opportunity employer, and we do not tolerate discrimination based on characteristics such as age, gender, gender identity and expression, genetic status, sexual orientation, race, ethnicity, national origin, religion, disability, military status, family status, or any other protected category under federal, state, or local law. Position Details Now Hiring LocationBedford, MA Employment TypeFull-Time DepartmentEngineering Salary Range$90,000 - $115,000 Apply Now Share This Career * * * * Ready to Apply? Click the button below to submit your application for this position. 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View Position Career Senior Validation Engineer Full-Time•Engineering•Bedford, MA This position is responsible for leading and performing the Bedford Site's Validation projects that includes start-up, commissioning, qualification, validation and revalidation for facility, equipment, critical… View Position Products Navigation" data-detect-dark-bg="true">Products * Regenerative Solutions * OA Pain Management * Our Technology Resources Navigation" data-detect-dark-bg="true">Resources * Literature & Videos * News & Blog * Just For Patients * Events * Certifications * Form 1095-C * Instructions for Use * Find a Doctor Company Navigation" data-detect-dark-bg="true">Company * About Anika * Meet Our Team * Our Story * Join Us Connect Navigation" data-detect-dark-bg="true">Connect * Investor Relations * Contact Us * Find a Rep Follow Us * LinkedIn * Instagram * Facebook * X * YouTube 3 Media Web Solutions, Inc 2026 Anika Therapeutics. All rights reserved. Privacy Policy Terms of Use Legal

Created: 2026-04-02