Easter Seals Jobs

Manager, Incoming Inspection - 2406203320W

Description

Johnson & Johnson is recruiting for a Manager, Incoming Inspection, located in Danvers, MA, USA.

This is a unique opportunity to join a world-class team at Johnson & Johnson. As the Manager of Incoming Inspection, you will have a critical role in ensuring the flawless quality of our products and driving continuous improvement initiatives. This is an exciting role that offers the chance to make a significant impact and contribute to the success of our ambitious goals!

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

KEY RESPONSIBILITIES:

• Lead a team of supervisors and incoming engineers to ensure the efficient and effective inspection of incoming materials and components. Our commitment to exceptional quality starts with leadership.

• Develop and implement standard operating procedures (SOPs) for incoming inspection processes. Your expertise will enable us to maintain consistency and accuracy in our inspection protocols.

• Collaborate with teams from different departments to identify and address quality issues and non-conformances. Working closely with Supplier Quality Engineering, Supplier Engineering, Logistics and Product Development will enhance our ability to improve our products and processes.

• Support investigations into material review boards (MRB) and provide guidance on disposition.

• Monitor, analyze and report out inspection data to identify trends and implement corrective actions. Keen analytical skills will allow us to proactively address any potential quality concerns.

Qualifications

Education:

• A Bachelor's degree in Engineering or a related field is required, with equivalent experience also being considered. Although a Master's degree is preferred, it is not obligatory.

Experience and Skills

Required:

• Demonstrated ability in a quality engineering, manufacturing engineering or incoming inspection role, preferably within the medical device or pharmaceutical industry.

• 6 years of related work experience

• Experience in managing teams and driving process improvements. Leadership skills will empower your team to excel and continuously strive for excellence.

• Strong knowledge of quality management systems, FDA regulations, and ISO standards. Expertise in regulatory compliance will help us meet and exceed industry standards.

• Excellent analytical and problem-solving skills. Ability to analyze complex data and provide practical solutions will be crucial in maintaining our quality standards.

• Strong communication and collaboration skills to effectively work with diverse teams. The ability to collaborate with colleagues from various departments will be essential in maintaining a cohesive and efficient quality control process.

• Ability to lift up to 50 pounds. Your physical capabilities will ensure that you can perform the necessary tasks associated with the role.

Preferred:

• ASQ certification (e.g., CQE, CQA).

• Experience with non-conforming materials and MRB (Material Review Board) processes. Familiarity with MRB processes will enable you to efficiently manage non-conforming materials.

• Knowledge of statistical process control (SPC) and Lean Six Sigma methodologies. Using statistical analysis and continuous improvement methodologies will support our business growth and development.

• Experience with SAP or other ERP systems. Your familiarity with ERP systems will facilitate seamless data management and analysis.

Other:

• Proficiency in English is required.

• Limited travel may be required for training and collaboration purposes.

• Relevant certifications such as Lean Six Sigma or Certified Quality Engineer are preferred. Your certifications will enhance your ability to contribute to our continuous improvement initiatives.

• Experience in SAP (or other similar ERP systeim) is a plus

• This position is not unionized.

• Valid driver's license is required for this role.

For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com.

Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Primary Location NA-US-4887-Danvers

Organization ABIOMED Inc.(6942)

Job Function Quality Control

Req ID: 2406203320W