Quality Engineer II (Validation)

Becton Dickinson Medical Devices • Hunt Valley, MD

1d • Onsite

About The Position

The Quality Engineer II, Validation is responsible for supporting and maintaining Quality Systems across Media manufacturing plants, with a primary focus on validation writing, execution, and compliance. This role ensures consistent application of quality standards, drives continuous improvement initiatives, and partners cross-functionally to support manufacturing operations, product quality, and regulatory compliance.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us? To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers . Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Requirements

• Bachelor's degree in Biological Sciences, Chemistry, or other related science field.
• 2 years experience in Quality, Scientific Operations, or Engineering.

Nice To Haves

• Experience in technical writing and managing process and test method validations.
• Experience in a medical device or pharmaceutical manufacturing facility.
• Knowledge of automated systems for filling and packaging are a plus.

Responsibilities

• Develop, implement, and maintain Quality System procedures, Standard Operating Procedures (SOPs), and quality policies.
• Lead and execute validation activities, including change validations and recurring process/equipment qualifications for Media plants and IDAST.
• Monitor, trend, and analyze quality indicators for purchased materials, manufactured products, and distributed components.
• Assess Critical to Quality (CTQ) parameters and perform risk assessments to support product quality, process predictability, and decision-making.
• Apply statistical tools and data analysis techniques to identify root causes, resolve quality issues, and implement effective corrective actions.
• Initiate and support Corrective and Preventive Actions (CAPAs), including leading investigations and corrective action activities when required.
• Support process control initiatives and promote consistent manufacturing practices across operations.
• Identify and recommend continuous improvement opportunities to enhance product quality, operational efficiency, and compliance.
• Manage day-to-day Quality Management (QM) Engineering activities for assigned products and operational projects.
• Partner with manufacturing, engineering, and cross-functional teams to support product launches, process improvements, and quality initiatives.
• Ensure consistent implementation and application of Quality Systems for both new and existing product lines.
• Maintain compliance with FDA regulations, ISO standards, and other applicable quality and regulatory requirements.
• Support quality-related activities including change controls, product quality notifications, post-market activities, IVDR compliance, and customer complaint investigations.
• Utilize enterprise systems and quality tools to drive compliance, documentation accuracy, and process efficiency.
• Serve as a subject matter expert (SME) during internal and external audits, as needed.
• Foster collaborative and inclusive working relationships across departments that support Media manufacturing operations

Benefits

• Total Rewards program
• Competitive package of compensation and benefits programs
• Salary or hourly rate ranges reward associates fairly and competitively
• Regular review of salary ranges and factors
• Pay is based on the role and the necessary skills and education to perform it successfully
• Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location

What This Job Offers

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