Sr Mgr, Global Quality Assurance 1

We believe that diversity adds value to our business our teams and our culture. We are committed to equal employment opportunities fostering an inclusive environment where diversity makes us outstanding.

Help us lead one of the worlds largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries and a growing global team of over 20.000 people. Thats why we need aGlobal Quality Senior Manager like you.

What your responsibilities will be

Execute and ensure the effective implementation of Global Quality Assurance processes across Biopharma sites with a strong focus on packaging activities and final product release.
Provide operational global support to site Quality teams to ensure consistent application of QA processes standards and requirements
Coordinate and support the management of quality incidents deviations investigations and CAPAs.
Support and monitor batch release processes collaborating with Supply Logistics and other stakeholders to facilitate product flow and ensure timely release
Perform oversight of Quality Systems identifying risks and proactively escalating critical issues to Senior Management when required
Coordinate and contribute to global Quality projects and initiatives ensuring execution followup and delivery of defined objectives
Support internal and external audits and regulatory inspections ensuring proper preparation execution and followup of actions
Collect analyze and monitor Quality Metrics and KPIs preparing reports and trend analyses to support datadriven decisions
Promote harmonization consistency and best practices across Biopharma sites fostering a culture of continuous improvement and compliance
Supervise and coordinate Quality teams supporting capability development knowledge sharing and operational alignment across sites
Stay informed of applicable regulatory requirements and quality standards supporting their correct and timely implementation

Who you are

To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge skills education and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).

• Bachelors Degree in Health Sciences or a related field
• 5-10 years of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry
• Analytical and problem-solving abilities
• Excellent written and verbal communication skills
• Experience in project management
• Ability to facilitate change
• Develops collaborative working relationships
• Good understanding of regulatory requirements and quality standards relevant to Biological products
• International experience
• Willingness to travel internationally as needed
• Ambitious results-oriented business-minded person

What we offer

It is a brilliant opportunity for you Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at. If you are interested in joining our company and you have what it takes for such an exciting position then dont hesitate to apply!

We look forward to receiving your application!

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program: Hybrid Model

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package

Contract of Employment:Permanent position

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