Manufacturing Engineer (multiple Openings)

Johnson & Johnson Johnson & Johnson · Pharma · Anasco, Puerto Rico +1

Manufacturing Engineer role at Johnson & Johnson focused on supporting the manufacturing organization, optimizing processes, and ensuring production goals are met. Responsibilities include technical activities for new/improved products/processes, problem analysis, validation support, and troubleshooting equipment. Requires a Bachelor's degree in Engineering and at least two years of experience. Experience in Medical Device or Pharmaceutical industry is preferred, along with knowledge of regulatory compliance.

What you'd actually do

  1. Initiates and completes technical activities to new or improved products or processes, for current programs, next generation programs and to meet strategic goals and objectives of the company.
  2. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.
  3. Incorporates business policies and procedures into task completion. Understands the business needs of the company and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends.
  4. Cultivates internal and external network of resources to complete tasks. Serves as a resource in the training of new engineers and employees.
  5. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters. Acts as spokesperson to customers on business unit current and future capabilities.

Skills

Required

  • Bachelor's degree in Engineering
  • Minimum two (2) years of experience in Engineering
  • Strong knowledge on Statistics
  • Computer literate
  • Good communication skills
  • Fluent in English and Spanish
  • Good interpersonal skills
  • Strong skills on problem solving/root cause analysis
  • Knowledge of regulatory compliance with all local and federal agencies i.e., FDA, ISO, OSHA, etc.

Nice to have

  • Experience in Medical Device or Pharmaceutical industry
  • Certification in CQE or Six Sigma Black Belt Project Management

What the JD emphasized

  • process/equipment validations
  • regulatory compliance with all local and federal agencies i.e., FDA, ISO, OSHA, etc.