NHS Human Services, Inc.

Manufacturing Supervisor - 2406198219W

Description

Manufacturing Supervisor

About Johnson&Johnson

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/.

Job summery

Within operations, high quality products are manufactured in a safe work environment. The manufacturing supervisor is responsible for achieving and maintaining the production output as documented in the master production schedule or shipment schedule, confirming to; safety, cGMP and lean. (S)He will be working with other manufacturing supervisors. (S)He will be responsible for the core business for the department. (S)He creates a culture in which continuous adhering to, and improvement of, standards is the standard. The manufacturing supervisor leads, supports and coaches a team of colleagues. (S)He ensures a learning and stimulation work environment.

Duties & responsibilities

Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Supports the introduction of New Products/Equipment

• Providing User Requirements (URS) to (line) Engineering

• Identifies documentation affected (SOP’s and Work Instructions)

• Supports training for manufacturing operators in the correct use of the equipment

• Supports the qualification of the equipment

• Leads a Team as part of the End to End production

The supervisor is responsible for:

• Assigning operators per team

• Timely identification of the need for additional Asset(s)

• Ensures the month targets are met according MPS (manufacturing Production Schedules)

• Review and report the performance of the individual team leaders to the next management level and hold at a minimum the 5 performance conversations

• Performs other duties assigned as needed

CGMP, EHS&S, EN LEAN

The work is carried out under strict cGMP conditions. The operator ensures a safe, healthy and sustainable working environment. The execution of tasks, the organization of the work and the continuous improvement of efficiency, effectiveness, quality and cGMP and EHSS compliance are supported by Lean techniques and concepts. The operator has good knowledge of cGMP, EHSS and Lean, at the level appropriate for this position, is trained in the internal procedures and always follows these, as well as other internal standards. The Associate Manufacturing Operator identifies shortcomings and opportunities for improvement. He/she occasionally carries out improvement initiatives that are practical in nature and do not require support from other departments.

Qualifications

Experience and education

• Minimum Educational level: HBO

• Minimum 5 years of working experience

• Experience in the Medical Device industry or medical field

• Computer skills in relation to usage to automation software such as Excel, Windows, ERP software

• Verbal and written communication skills in English and Dutch, business/financial acumen, six sigma and process excellence tools/methodologies, presentation skills

• Performs on pre determined schedule level checks to ensure quality and reliability

Skills

• Detailed knowledge of the manufacturing Process, end to end

• Familiar with the CGMP requirements insofar as these relate to his / her work

• Responsible for being trained at all times in the applicable procedures

• Familiar with the EHS & S requirements insofar as these relate to his / her work. Responsible for being trained at all times in the applicable procedures

• Is able to identify continuous improvements in (work) processes and communicate these to line engineer

• Sets the right priorities, where necessary in close coordination with those involved

• Is focused on ensuring a thorough and flawless production process to meet the highest standards

• Builds strong and productive relationships with all different departments and layers within the Leiden site and within the J&J network. Shows respect for and listens to others. Is aware of their own behavior and the effect on others. Is able to effectively present improvement proposals to stakeholders and thereby guide the decision-making process

• Acts from the company's interests and knows how to frame initiatives within the objectives of the department and the site.

DE&I Statement

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Primary Location Europe/Middle East/Africa-Netherlands-South Holland-Leiden

Organization Mentor Medical Systems, B.V. (8808)

Job Function Manufacturing Assembly

Req ID: 2406198219W