LOCATION:

Cartago, Costa Rica, CR
Job Family: Manufacturing
Country/Region: Costa Rica
This is a permanent-full time position to work in our Cartago Site, located in Zona Franca La Lima. Relocation is not allow for this position.
Our Value Stream Managers lead, plan, control, coordinate all functions within the Value Streams and ensure that products comply with regulations and company requirements. They manage the production of the area’s product(s) and manage the area’s processes with the given resources in line with the production plans, with the expected safety and quality, at the lowest cost level. Follow up / maintain the machines, measuring devices from maintenance point of view and ensure the right technical condition. Planning the related processes and resources. Implement and improve Lean processes to achieve the highest utilization of the resources.
The Value Stream Manager is responsible for keeping the fulfilment of all related instructions, standards in the area. Responsible for tracking the related materials and for finding the root cause of scrap and losses. Responsible for keeping the area’s material handling equipment in a good condition – organize the change if needed.

HUMAN RESOURCES:

Ensure the most efficient given human resources to maintain operations within the Value Stream (VS).
Plan and execute the people development focused on required competencies.
Scheduled frequent meetings / discussions with team members to inform and manage them.
Headcount planning and execution of actions.
Manage disciplinary process when applicable according to Coloplast and legislation.
Planning and execution of overtime according to the best interests of the company.
Comply and adhere to Coloplast standard procedures, as well as safety and EHS related rules.
Responsible for the creation of Job descriptions and Training plans of all direct reports
Responsible to request all necessary accesses and specific roles to Coloplast systems for direct reports
Any additional tasks requested by the direct leader

ESSENTIAL QUALIFICATIONS:

Bachelor’s degree (B. A. / B.S.) with a Masters degree preferred.
Proven experience managing cross/functional teams and an organization larger than 200 collaborators including direct, indirect and support personnel.
Manufacturing and/or medical devices industries experience
Experience improving manufacturing operations using Lean and Six Sigma techniques. Certification on Lean or Six Sigma is desirable.
Experience with MES or other system to track and analyze production operations.

PREFERRED QUALIFICATIONS:

General knowledge of mechanical and electrical systems.
Experience working with inventory management systems.
Ability to manage multiple projects simultaneously.
Knowledge of PowerBI.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:

Must be flexible with work schedule.
Proficient on production capacity analysis.
Strong written and verbal communication skills
Change facilitation/Lean transformations.
Computer skills (Microsoft Office Suite, ERP Systems)
Good English knowledge.
Problem solving skills.
Experience working with inventory management systems.
Ability to manage multiple projects simultaneously.
Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16.000 people and with products available in more than 143 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things.
Coloplast is committed to being an inclusive organization, where people bring their differences to work each day, fulfil their potential and have a strong sense of belonging because – and not despite – of their differences. We therefore encourage all qualified candidates to apply regardless of gender, age, race, nationality, ethnicity, sexual orientation, religious belief or physical ability.
Visit us on Coloplast.com.
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RESPONSIBLE FOR THE FOLLOWING WITHIN THEIR AREA:

Implementation of requirements in the corporate quality system
Clearly defining responsibilities and authority for relevant activities described in the quality system.
Ensure awareness of the Quality policy
Ensure awareness of their contribution to the effectiveness of the Quality system and the benefits of improved performance
Ensure awareness of implications for not conforming with Quality requirements
The identification of needs and preparation of instructions, where necessary.
Ensuring that the required resources and competences are available.
Taking action if requirements from the quality system and/or regulatory requirements are not complied with.