Cirtec Medical

Validation Engineer II

LOWELL, MAPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Cirtec Medical

  • Job overview

    The Validation Engineer II at Cirtec Medical is responsible for process validation activities to ensure manufacturing compliance and improvement of medical device production processes.

  • Responsibilities and impact

    The role involves writing and analyzing validation studies, supporting quality systems, participating in regulatory inspections, coordinating with multiple teams, and managing project schedules and costs.

  • Compensation and benefits

    The salary range is $80,000-$100,000 with benefits including healthcare, dental, vision, wellness programs, paid time off, 401(k) with company match, and career development opportunities.

  • Experience and skills

    Requires a bachelor's degree in engineering or related field with 2-5 years of experience, knowledge of cGMP, validation study authorship, problem-solving skills, and ability to collaborate across functions.

  • Career development

    The company offers training and career development programs to support growth at every career stage.

  • Work environment and culture

    Cirtec Medical promotes a culture of innovation, respect, transparency, and communication, aiming to create an enjoyable and supportive work environment.

  • Company information

    Cirtec Medical is a leading provider of manufacturing solutions for complex Class II and III medical devices with over 30 years of experience in design, development, and manufacturing.

  • Team overview

    The position works closely with Quality Assurance, Manufacturing, and Engineering teams to enhance manufacturing processes.

  • Unique job features

    The job includes unique opportunities to work on complex medical device manufacturing validation and participate in regulatory inspections.

Company overview

Cirtec Medical is a leading provider of comprehensive outsourcing solutions for complex medical devices. They specialize in the design, development, and manufacturing of active and passive implantable devices, minimally invasive surgical devices, and other critical medical technologies. Cirtec makes money by offering end-to-end services, including product development, regulatory support, and full-scale production for medical device companies. Founded in 1988, Cirtec has grown through strategic acquisitions and partnerships, establishing a strong presence in the medical device industry. Their expertise and integrated approach help clients bring innovative medical solutions to market efficiently and effectively.

How to land this job

  • Position your resume to highlight your experience authoring and completing process validation studies, emphasizing familiarity with cGMP requirements and validation documentation.

  • Focus on collaboration skills with cross-functional teams such as Quality Assurance, Manufacturing, and Engineering to demonstrate your ability to implement validation activities effectively.

  • Apply through multiple channels including Cirtec Medical's corporate careers page and LinkedIn to maximize your chances of being noticed for the Validation Engineer II role.

  • Connect with current Cirtec Medical employees in the Quality or Validation divisions on LinkedIn; start conversations by commenting on recent company projects or asking about their experience with process validation challenges.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'process validation,' 'cGMP,' 'CAPA,' 'risk assessment,' and 'equipment installation' to ensure it passes initial screenings.

  • Use Jennie Johnson's Power Apply feature to automate tailored applications, identify the best platforms to apply through, and find relevant LinkedIn connections, saving you valuable time during your job search.

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