LOC Quality and MAH EU Specialist (m/f/d)

Job title:

LOC Quality and MAH EU Specialist (m/f/d)

Company:

Takeda

Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s and . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:As Local Quality and MAH (Marketing Authorization Holder) EU Specialist you perform the Quality MAH obligations for Takeda Pharma A/S participating in the maintenance of Local and Nordic actions. In this multifaceted role, you will be responsible for change control, deviation, CAPA management, trainings, document management as well as audits and self-inspections (internal and external) among other things. You work as a deputy responsible person in Denmark as agreed with and delegated from the RP and report to Gitte Hjelvang, the Head of Quality DK & Nordics bei Takeda.How you will contribute:Product Quality Review and Marketing Authorization:Maintain overview of Takeda Pharma A/S MA ownership including PQR reviewPrepare, maintain and perform PQR review annual plan.Stakeholder management with internal and external partnersPrepare monthly the KPI for PQR and Quality agreement.Processing of deviations, CAPA’s and change control:Act as aTrackWise (TW) owner, subject matter expert (SME) and quality approverPrepare and participate Audits and inspection observationsInitiatiate, own, evaluate and review deviations, CAPAs and change controls in TrackWiseAct as quality approver locally as well as cross borders in the NordicsGeneral responsibilitiesBe part of LOC Quality CouncilTake care of proper archiving, documentation, and data integritySupport projects to contribute to the compliance with GDP regulation in LOC Denmark.Take care of proper archiving, documentation and data integrity relatedWhat you bring to Takeda:University degree in Life Sciences or a related discipline, pharmacy preferredExperience from the pharmaceutical industry (GXP)Excellent knowledge in local and international GMP / GDP regulationsStrong communication and stakeholder management skills.Fluent English (C1) and Denish is a mustMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.Empowering our people to shine:Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.LocationsDNK – VallensbækWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Expected salary

Location

Vallensbæk, Hovedstaden

Job date

Thu, 01 Aug 2024 01:34:43 GMT

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