Data Integrity Project Specialists

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Job ID SR0034164
Date posted 03/19/2019
Location:Neuchâtel, Canton of Neuchâtel

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine.

Here, everyone matters, and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

Data Integrity Project Specialists

11-month assignment (May 2019 – April 2020)

Takeda’s Neuchatel Manufacturing plant is looking for two highly motivated Project Specialists for a period of 11 months to work on project focused on Data Integrity.

Your mission

Within the Manufacturing support department, the purpose of this role to provide the technical expertise needed to participate in a Data Integrity project within the manufacturing process and to act as a catalyst for continuous improvement.

Essential Duties & Responsibilities

• Support the Data Integrity project for the whole manufacturing plant
  
  
  
  • Participate in the meetings related to this project
  
  
  • Follow-up on the assigned actions related to the scope of this project
  
  


• Lead, perform and review  risk/gap assessments related to the manufacturing equipment and associated data.


• Work on actions linked to production-related gap and risk assessment : participate in change control and documentation updates activities


• Work on actions linked to gap assessment and risk assessment (production related)


• Perform quality and manufacturing technical aspect reviews for the equipment

Required Skills

• Demonstrated experience in manufacturing and/or data integrity projects


• Confirmed experience with automated systems used in biotechnology industry


• Expertise in Quality/Compliance within an FDA regulated/GMP manufacturing field required


• Ability to provide solutions to satisfy business objectives and cost implications within timelines


• Structured systems thinking with good technical understanding of operations


• Ability to think and act cross-functionally, interacting with experts, SME’s, engineers etc.


• Project management training or experience is an asset (from URS to implementation)

Personal qualities

• Interpersonal skills, self-motivated, capable of analyzing and solving problems


• Great team player prepared to work in and embrace a team-based culture and more specifically within the manufacturing teams directly on the production floor


• Excellent oral and written skills in English and French


• Ability to describe processes and qualifications and to translate them into clear, precise reports

Working Environment

• While this is a day-time job, must be able to work on occasions in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.

Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda’s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.

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