Senior Supplier Management Engineer - m/f - Pharmaindustry
Core Informatics
Regensburg, Germany
vor 16 Tg.

Austria - LinzNetherlands - TilburgNetherlands - GroningenItaly - MonzaItaly - FerentinoFrance - BourgoinGermany - Regensburg

Job DescriptionAs a member of the Global Supplier Quality organization, the Senior Supplier Management Engineer will be a key contributor into the global supplier performance management program at Thermo Fisher.

The Senior Supplier Management Engineer will be responsible for implementing procedures and best practices that focus on mitigating risk in the supply base, improving Supplier performance, and driving resolution to escalated Supplier deviations.

Specifically, the responsibilities include supplier deviation management, risk identification and reduction, quality and supply chain improvements, and relationship management with internal and external stakeholders.

The Senior Supplier Management Engineer will have experience in Pharmaceutical / Medical Device manufacturing or similar field and will possess technical capabilities, problem solving knowledge, project management skills and procurement acumen.

Essential Functions : Travel up to 50%Travels to and from supplier locations to resolve escalated Manufacturing, Quality, Technical and supply issues and investigations, as well as facilitate overall improvements to proactively prevent supplier issues.

Utilizes enhanced problem-solving skills (six sigma) to determine true root cause and to develop and implement irreversible corrective actions.

Coordinates, communicates and oversees general technical matters pertaining to suppliers, including understanding and optimizing component / material usage and upskilling suppliers to provide improved materials and services.

Provides efficient and effective solutions and CAPA management for escalated supplier issues.Provides supplier investigation ownership related to escalated supplier complaintsResponsible for communicating escalated issues to the Global Supplier Quality Leadership Team Participates in periodic business and relationship review meetings with problematic suppliers.

Serves as a primary point of contact to legacy Patheon sites and suppliers in the region. Responsible for managing a data driven Global Supplier Management program that focuses on identifying and mitigating risk across the direct material supply chain.

Works across functional boundaries to identify business needs and establish best practices.Must understand worldwide regulatory requirements and cGMPs.

Ensures policies and practices are in place to meet compliance requirements of relevant standard including (ISO 9002,ISO13485, cGMP).

Education : A minimum of a Bachelor’s Degree is required in Engineering, Science, or Business Experience : A minimum of 5-

10 years of relevant experience in a GMP environment, in any of the following industries : Pharmaceutical, Medical Device, OTC Drug, Cosmetic and / or Food and Dietary Supplements, is required.

Minimum of 5 years’ experience in Procurement and / or Quality.Demonstrated problem-solving skillsKnowledge of cGMPs, technical writing, data management, collection, and analysisSigma Black Belt, Green Belt or Yellow Belt certificationExperience in CAPA management systems (i.

e. TrackWise)Experience in a matrix organizationExperience in driving continuous improvement with a track record of achieving results.

Experience in Supply Chain Management and capacity assessment a plus. Equivalency : Equivalent combinations of education, training, and relevant work experience may be considered.

For this role, we offer an attractive salary that matches your qualifications and experience. Please note that for legal reasons we have to point out that for this position according to the collective agreement for the chemical industry the monthly gross salary is at least € 3.163,33.

As a member of the Global Supplier Quality organization, the Senior Supplier Management Engineer will be a key contributor into the global supplier performance management program at Thermo Fisher.

The Senior Supplier Management Engineer will be responsible for implementing procedures and best practices that focus on mitigating risk in the supply base, improving Supplier performance, and driving resolution to escalated Supplier deviations.

Specifically, the responsibilities include supplier deviation management, risk identification and reduction, quality and supply chain improvements, and relationship management with internal and external stakeholders.

The Senior Supplier Management Engineer will have experience in Pharmaceutical / Medical Device manufacturing or similar field and will possess technical capabilities, problem solving knowledge, project management skills and procurement acumen. Essential Functions :

5 Reasons to Work at Thermo Fisher Scientific

  • Travel up to 50%
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  • Travels to and from supplier locations to resolve escalated Manufacturing, Quality, Technical and supply issues and investigations, as well as facilitate overall improvements to proactively prevent supplier issues.
  • Utilizes enhanced problem-solving skills (six sigma) to determine true root cause and to develop and implement irreversible corrective actions.

  • Coordinates, communicates and oversees general technical matters pertaining to suppliers, including understanding and optimizing component / material usage and upskilling suppliers to provide improved materials and services.
  • Provides efficient and effective solutions and CAPA management for escalated supplier issues.
  • Provides supplier investigation ownership related to escalated supplier complaints
  • Responsible for communicating escalated issues to the Global Supplier Quality Leadership Team
  • Participates in periodic business and relationship review meetings with problematic suppliers.
  • Serves as a primary point of contact to legacy Patheon sites and suppliers in the region.
  • Responsible for managing a data driven Global Supplier Management program that focuses on identifying and mitigating risk across the direct material supply chain.
  • Works across functional boundaries to identify business needs and establish best practices.
  • Must understand worldwide regulatory requirements and cGMPs.
  • Ensures policies and practices are in place to meet compliance requirements of relevant standard including (ISO 9002,ISO13485, cGMP).
  • A minimum of 5-10 years of relevant experience in a GMP environment, in any of the following industries : Pharmaceutical, Medical Device, OTC Drug, Cosmetic and / or Food and Dietary Supplements, is required.
  • Minimum of 5 years’ experience in Procurement and / or Quality.
  • Demonstrated problem-solving skills
  • Knowledge of cGMPs, technical writing, data management, collection, and analysis
  • Sigma Black Belt, Green Belt or Yellow Belt certification
  • Experience in CAPA management systems (i.e. TrackWise)
  • Experience in a matrix organization
  • Experience in driving continuous improvement with a track record of achieving results.
  • Experience in Supply Chain Management and capacity assessment a plus.
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