philip morris - quality compliance specialist in Neuchatel

posted
contact
Quentin Terrisse, Randstad Inhouse Services PMP Neuchâtel
job type
temporary
apply now

job details

posted
location
neuchatel, neuchâtel
sector
Industrie
job type
temporary
reference number
113866-24816
contact
quentin terrisse, randstad inhouse services pmp neuchâtel
phone
058 242 15 69
apply now

job description

For our client Philip Morris SA in Neuchâtel, we are seeking a:

Quality Compliance Specialist

(100% - Long Term contracted assignment)

The purpose of this role is to support the implementation, maintenance, and continuous improvement of Quality Assurance (QA) program for ISO 17025 to demonstrate to Management that the laboratory activities, facilities, equipment/instrumentation, personnel, methods, procedures, records and systems are under control through QA verification/review, audit and/or inspection. It also implies to support Quality Compliance Team relating to GLP & GCLP activities.

Responsibilities:

ISO 17025 Quality Implementation:
  • Perform internal audits and audits of supplier in accordance to relevant guidelines, including PMI expectations
  • Actively contribute to the entire accreditation process, including the preparation phase, activities during the inspection, and any necessary follow-up
  • Assist in internal and regulatory audits/inspections readiness, in preparation, during the conduct and at the conclusion of the audit by ensuring all ISO 17025 related activities are under control at all time
  • Support the execution of governance for Reduced Risk Products (RRP) and Conventional Cigarettes (CC) for PMI, ensuring adherence with the QMS according to internal and external standards
  • Perform QA review of new and existing controlled-documents for completeness, accuracy, data integrity and maintenance in compliance with ISO 17025 such as standard operating procedures (SOPs), work instruction and forms/templates
  • Contribute to the maintenance, testing, and improvement of Systems related to main accountabilities

Quality Compliance Team support:
  • Support document and record management activities
  • Support archiving and e-archiving process in accordance to ISO 17025 standard and any other relevant requirements
  • Support training activities by acting as back-up Functional Admin for LMS (Learning Management System)
  • Provide training on systems and processes owned by Quality Compliance.

qualification

  • Education: University in Life science or any relevant field or equivalent skills through demonstrated experience
  • 1-3 years' experience in quality organization, preferably within a GxP environment
  • Proven knowledge of Quality Management Systems and related external standards (ISO, GxP) and experience in maintenance of quality management systems and continous improvement
  • Proven auditing experience in ISO 17025, GLP or in the area of pharmaceutical or life science
  • Experience in life science, in a R&D function preferred
  • Excellent verbal and written communication skills, with emphasis on technical writing
  • Good planning and organizational skills.
  • Experience in project management in a cross-functional and international environment is preferable
  • Able to deal with ambiguity, autonomous and highly action oriented
  • Fluent in English and French languages.
  • Start date: As soon as possible

If you are interested in this challenging position, please do not hesitate to send us your CV, motivation letter, latest certificates and the date of your availability. Only online applications will be considered. We look forward to your application that will be treated with full confidentiality.

Please note that a UE27/AELE nationality or a valid Swiss Work Permit are required for this position