Quality Specialist (f/m/d), Part Time (20 hours a week), Hybrid

Takeda; Wien; Hybrid; EUR 40 000 - 60 000; Teilzeit

Zusammenfassung

Takeda is seeking a part-time Quality Specialist in Vienna to ensure compliance with quality assurance regulations in Distribution and Sales. The role involves managing document systems, conducting audits, and supporting local quality activities. Ideal candidates should have a scientific degree, three years experience in pharma, and be fluent in German and English, contributing to an inclusive workplace committed to better health outcomes.

Leistungen

Competitive salary

Flexible work from home options

In-house job rotation program

Employee referral and recognition programs

Qualifikationen

• Bachelor's or Master's degree in a scientific or health sciences field.
• Experience in pharmaceutical companies over the last 3 years.
• Fluency in spoken and written German and English.

Aufgaben

• Manage electronic document management and training systems.
• Coordinate Gap Assessments of global processes.
• Support health authority communications regarding product quality issues.

Kenntnisse

Communication

Organizational Skills

Interpersonal Skills

Ausbildung

Bachelor's or Master's in Scientific Field

Jobbeschreibung

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Quality Specialist (f/m/d), Part Time (20 hours a week), Hybrid, Vienna

Client: Takeda

Location: Vienna, Austria

Job Category: Other

EU work permit required: Yes

Job Reference: 4ce7c720629a

Job Views: 6

Posted: 21.06.2025

Expiry Date: 05.08.2025

Job Description:

About the role:

As a Quality Specialist, you will support the Quality area of Distribution and Sales for Austria in all aspects of Quality Assurance in accordance with Austrian regulations and Takeda. You will report to the Manager, Quality Assurance.

How you will contribute:

• Manage electronic document management and training systems as the LOC administrator.
• Maintain the LOC QMS, including coordinating Gap Assessments of global processes.
• Create and maintain local SOPs and other quality documents (e.g., contracts, quality agreements).
• Support local deviations, CAPAs, escalations, and field corrective actions.
• Handle local quality surveillance activities such as returns, market actions, complaints, inquiries, and customer qualification.
• Participate in internal and external audits.
• Assist in preparing monthly LOC Quality reports.
• Support health authority communications regarding product quality issues affecting Austria.
• Promote enterprise thinking, innovation, and trust-building to serve patients better.
• Participate in LOC and GQ projects as assigned by the Line Manager.

What you bring to Takeda:

• Bachelor's or Master's degree in a scientific or health sciences field (biotech, pharma, chemistry, biology).
• Experience in pharmaceutical companies over the last 3 years, with exposure to audits.
• Fluency in spoken and written German and English.
• Strong communication and organizational skills.
• Excellent interpersonal skills to build relationships, challenge thinking constructively, and work collaboratively.
• A lifelong learning mindset and ownership of personal development.

What Takeda can offer you:

• A competitive salary starting at €3,307.50 gross per month (full-time, collective wage agreement for the chemical industry), depending on experience and qualifications.
• Support with parental leave, dad month, bilingual company kindergarten.
• Flexible work from home options depending on the role.
• In-house job rotation program.
• In-house canteen with discounts or meal vouchers.
• Employee referral and recognition programs.
• Takeda Resource Groups.
• Medical checkups and fitness center access.

More about us:

Takeda is committed to transforming patient care through innovative pharmaceuticals and patient support programs. Recognized as a Global Top Employer, we foster an inclusive, collaborative workplace dedicated to delivering Better Health and a Brighter Future worldwide.

Empowering our people to shine:

We are committed to diversity and equal employment opportunities for all employees and applicants, regardless of race, color, religion, sex, sexual orientation, gender identity, parental status, national origin, age, disability, citizenship, genetic information, marital status, or any other protected characteristic.