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Mid Research and Development (R&D) Engineer

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Heredia, H

  1. Research & Development
  1. Full-time
R00134173

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.


Job Description

Position Purpose Lead, collaborate, and execute regional and global product and process development initiatives (NPI and MPS) within the R&D function, focusing on medical devices. Guide projects from concept inception, working intimately with cross-functional experts—including physicians and researchers—to design and refine innovative products born from scientific ideas and publications, bringing transformative solutions from vision to reality. Manage all phases from Design Validation & Verification (DVV) to Process Validation, ensuring manufacturability and compliance throughout the development lifecycle.

Major Responsibilities

  • Perform as a key member on the Global Core Team for breast-related medical device projects, supporting both Marketed Product Support (MPS) and New Product Introductions (NPI).
  • Lead and collaborate on product and process development activities, serving as an essential participant in the design and development sub-teams.
  • Spearhead early-stage product ideation, engaging directly with clinicians, scientists, and cross-functional teams to shape solutions founded on emerging needs and the latest scientific advances.
  • Partner with engineering, manufacturing, and marketing departments to evaluate new materials, review specifications, and integrate novel technologies with rigorous scientific and technical acumen.
  • Support and/or lead technical initiatives related to product design, compliance with regulatory agencies, and documentation for new or enhanced products.
  • Contribute to organizational objectives by supporting change controls, audits, CAPAs, complaint investigations, regulatory and marketing inquiries, and associated data generation.

Qualifications

Education

  • Bachelor’s degree or higher in Engineering (Chemical, Mechanical, Materials, Physics) or related sciences (Biology, Chemistry).
  • Master’s degree is highly desirable.
  • Advanced English proficiency (B2/B2+ or higher), capable of working in an international, scientifically driven environment.

Skills & Experience

  • Minimum 3 years’ experience in Product Development, Manufacturing, Process Engineering, or Quality within the Medical Device Industry.
  • In-depth knowledge of Quality Management Systems and global regulations (GMP, QSR, FDA, CAPA, ISO).
  • Skilled in technical writing and documentation, and proficient in Microsoft Office; experience with Minitab, SolidWorks, or AutoCAD is desirable.
  • Proven experience with design control, medical device manufacturing, and process development.
  • Familiarity with plastics, rubber, or silicone design and processing methods; understanding of materials selection, test methods, and physical/chemical characterization.
  • Competence in risk management methodologies, such as FMEA, as well as equipment qualification and process validation.
  • Demonstrated ability to work collaboratively with multidisciplinary teams, maintaining confidentiality and performance under regulatory environments.
  • High level of flexibility, technical rigor, and a drive for real, tangible results—transforming visionary concepts into concrete solutions, no matter the challenge ('as if taking a washing machine to the moon').

Additional Information

At AbbVie, we are committed to cultivating a work culture that promotes inclusion, diversity and personal growth. We recognize that our collective success is based on the individual well-being of our employees and that is why

we have designed a benefits package with every aspect of their lives in mind.

  • Enhanced Health and Wellness Coverage: Our administrative staff has comprehensive medical and dental insurance, ensuring peace of mind for you and your loved ones.
  • Flexible Hybrid Work Model: For eligible positions within our administrative staff, we adopt a hybrid work scheme that allows you the convenience of teleworking for two days a week.
  • Life Insurance: Secure your family's future with our life insurance policy.
  • Educational Advancement: Invest in your future with our scholarship program available to employees and their
  • dependents.
  • Employee Assistance Program (EAP): Access professional support with our comprehensive EAP, which offers psychological, legal and financial counseling.
  • Community and Social Commitment: Make a difference with a paid volunteer day, which allows you to contribute to the community during the company's working hours.
  • Employee Stock Purchase Plan: Participate in our company's success by buying shares at a special price exclusive to employees.
  • Solidarity Association: Join a community focused on mutual aid and enjoy the benefits that come with being a member. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html