Site Quality Head, Hobro

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Nordjylland

Job Description


Site Quality Head – Pharmaceutical Production Plant

Takeda, Hobro

JOB PURPOSE:

The Site Quality Head is a key member of the Site Leadership Team and independently organized with reference to Region Quality in Europe.

The Site Quality Head is responsible for setting and executing the site’s Quality strategy and Quality Culture activities with focus to meet or exceed quality expectations. The Quality function consists of QC, QA, Quality Systems and Compliance and Quality Improvement, in total 13 employees.

Takeda – Better health, Brighter Future
Takeda is the biggest supplier of RX and OTC products in Denmark. Approximately every 6. Package delivered from the pharmacies in Denmark are coming from Takeda. By working at Takeda, you make a positive difference for thousands of patients and for yourself.

At the plant we produce various bulk tablets, which are packed and distributed in collaboration with other plants in our network.

Takeda is among the top 10 pharma companies in the world and we have a network in more than 70 countries in Europa, USA, Latin-American, Afrika, Middle east and Asia. You can read more here.

RESPONSIBILITIES:

The responsibilities of the Site Quality Head include:

  • Lead Quality Organization, QC, QA, QSC, QI
  • Implement/maintain Quality System
  • Ensure Qualification and Quality Agreements with main suppliers, customers and host audits at the site
  • Communication internally and externally (outside Hobro) on Quality Related matters
  • Member of Site Leadership team with responsibility to support daily business and tactic- and strategic development
  • Defining and monitoring strategic objectives for the Quality function in line with site and Global Quality objectives.
  • Leading change and continuous improvement for the Quality function.
  • Leading the site Quality Culture program and embedding a real culture of quality throughout the site.
  • Defining and ongoing monitoring of the Quality budget (operational and capex).
  • Resource planning and monitoring of resource requirements within Quality.
  • Mentoring Quality personnel will be part of the role
  • Preferably Qualified Person, responsible for product quality at Takeda Hobro

EDUCATIONAL REQUIREMENTS AND EXPIRIENCE:

  • Primary Degree in a scientific discipline preferably Cand Scient, Pharm
  • Minimum of 7 years’ experience in the pharmaceutical industry
  • QC laboratory experience is strongly desired

SKILLS/COMPETENCIES:

  • Strong Leadership and Interpersonal skills
  • Excellent knowledge of cGMP and preferably QP experience
  • High level of initiative
  • Excellent verbal and written communication skills in Danish and English
  • Ability to adapt to changing priorities, working in complex organizations and ability to creatively come up with innovative solutions
  • Excellent mentoring skills and the ability to bring a team together

Does this sound interesting?
If you have questions to this position, you are welcome to contact Site Head, Annelise Olsen, at telephone +45 2777 9757.

We look forward to hearing from you


Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Nordjylland

Jobbet er oprettet på vores service den 15.4.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Øvrige
  • Nordjylland
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