Global Quality Investigation Job Details | STADA Arzneimittel AG

STADA; Sant Just Desvern; Presencial; EUR 40.000 - 65.000; Jornada completa

Descripción de la vacante

Join STADA, a global pharmaceutical leader, as a Global Quality Investigator. In this role, you'll ensure product quality by managing investigations and documents while collaborating with internal and external partners. Ideal candidates will bring a pharmacist or engineer background with robust experience in quality assurance and strong technical writing skills.

Formación

• Minimum 2 years of experience in quality roles.
• C1 proficiency in English.
• Mandatory investigation experience.

Responsabilidades

• Review and approve investigation reports.
• Manage GMP and quality document systems.
• Coordinate investigations with partners.
• Lead Quality Incident Committee Meetings.

Conocimientos

Investigative skills

Technical writing

MS Office proficiency

Educación

Pharmacist or pharmaceutical engineer

Descripción del empleo

GLOBAL QUALITY INVESTIGATION

Barcelona | Spain | Full-time | Permanent

ABOUT US

At STADA, we pursue the purpose of "Taking care of people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision, and values. With our wide range of products—Generics, Consumer Healthcare, and Specialties—we offer patients, doctors, and pharmacists a broad spectrum of therapeutic options.

Approximately 13,000 employees embody our values of Integrity, Entrepreneurship, Agility, and One STADA, aiming to achieve our ambitious goals and shape a successful future for our company. We continually expand our objectives in line with our ambitions and accomplish them with passion, commitment, and a growth mindset.

Would you like to be part of a successful international pharmaceutical company and grow with us?

RESPONSIBILITIES

• Review and approve investigation reports
• Manage systems for archiving GMP and quality documents
• Coordinate investigations with responsible partners (internal sites, global and local functions, CMOs)
• Review and evaluate investigations related to quality issues for products on the market
• Create, review, and approve reports for national competent authorities
• Lead Quality Incident Committee Meetings for risk assessment regarding product quality, especially for batches on the market, in case of OOS results/deviations, and monitor actions defined in the committee
• Serve as key contact for specific topics and communicate globally with group-owned production sites and contract manufacturers
• Maintain metrics to ensure correctness, integrity, and consistency of GxP critical quality data
• Lead and review continuous improvement projects and promote innovation ideas
• Contribute to global quality projects according to plan
• Monitor KPIs related to investigation processes. Act as process owner for NONC, CAPA, DEV, or ETM. Prioritize and lead continuous improvement initiatives and innovative solutions
• Act as deputy team leader in the absence of the team leader, gaining leadership experience by supporting and coordinating the team as needed

EXPERIENCE

• Pharmacist, pharmaceutical engineer, or equivalent scientific qualification with further professional development
• English proficiency – C1 mandatory
• At least 2 years of experience in QP, QA, or QC roles
• Investigation experience is mandatory
• Advanced knowledge of MS Office suite
• Ability to understand and discuss complex topics; strong technical writing skills
• Professional experience in the pharmaceutical industry or a similar quality-focused position

STADA offers a competitive environment for personal and professional development in a growing company full of opportunities. Our future projects require dynamic and proactive professionals capable of adding value in a changing environment.

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