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Group Associate Project Manager (m/f/d) - Quality Control

Group Associate Project Manager (m/f/d) - Quality Control

Group Associate Project Manager (m/f/d) - Quality Control

Group Associate Project Manager (m/f/d) - Quality Control

Octapharma Pharmazeutika Produktionsges.m.b.H.

Pharmazeutische Produkte, Arzneimittel

Wien

  • Art der Beschäftigung: Vollzeit
  • Vor Ort
  • Zu den Ersten gehören

Group Associate Project Manager (m/f/d) - Quality Control

Über diesen Job

Group Associate Project Manager (m/f/d) - Quality Control

Job ID: 61807
Career Level:

Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.

With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.

This position is limited until 01.02.2028.

Your main tasks and responsibilities

  • Manage and coordinate complex, cross-functional projects within the global QC network, ensuring timely delivery and alignment with corporate objectives
  • Develop project plans, define milestones, allocate resources, and monitor progress to ensure successful implementation
  • Collaborate with internal stakeholders across global functions and manufacturing sites to ensure seamless project execution
  • Identify risks and implement mitigation strategies to ensure operational excellence
  • Drive continuous improvement initiatives within QC processes and systems
  • Prepare and deliver clear, structured communication to senior management and project teams
  • Support global harmonization efforts and contribute to strategic decision-making in QC

Your expertise and ideal skill set

  • University degree in a scientific discipline (Master preferred)
  • Good understanding of analytical laboratory processes in the biopharmaceutical or life sciences field
  • Experience in pharmaceutical or biotechnological industry, global exposure is an asset
  • Project management skills and advanced proficiency in Microsoft Office and project management tools
  • Excellent written and verbal communication skills in English
  • Ability to manage multiple priorities and work effectively under pressure
  • Willingness to travel as required by project needs

Your department - where you make an impact

  • We, the Corporate Quality department, provides strategic alignment across local Quality Control departments, analytical method validation, and stability studies, ensuring efficient processes and regulatory compliance.

Thrive with us

  • Company restaurant & meal subsidy
  • Training & further education
  • Health promotion
  • Parking spaces and good public transport connections
  • Company and team events

Enjoy these attractive benefits! You can find all offers here: Benefits

The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.270,14 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.

It´s in our blood

We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.

Do you have any questions? Then get in touch with your contact person.

Larissa Amling

Unternehmens-Details

company logo

Octapharma Pharmazeutika Produktionsges.m.b.H.

Pharmazeutische Produkte, Arzneimittel

1.001-5.000 Mitarbeitende

Wien, Österreich

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