Quality Assurance Officer to AstraZeneca in Södertälje

Logent AB / Administratörsjobb / Stockholm
Observera att sista ansökningsdag har passerat.


Visa alla administratörsjobb i Stockholm, Solna, Lidingö, Sundbyberg, Danderyd eller i hela Sverige
Visa alla jobb hos Logent AB i Stockholm, Solna, Sundbyberg, Danderyd, Huddinge eller i hela Sverige

Publiceringsdatum
2020-10-05

Om tjänsten

About AstraZeneca

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration.

We are now seeking Quality Assurance Officer to join the Global Supplier Quality (GSQ) team.

About the position
Job description

The incumbent is responsible for compliance activities for GSQ supply chains and suppliers. They are responsible for all Quality activities that directly support execution of assigned Quality Management System elements.

QAOs will be assigned in discussion with their line management, key areas of responsibility, but will be expected to learn other areas of the quality system to help support the rest of the team during times of peak workload or holiday coverage.

This includes, but is not limited to, the Quality System oversight and/or performance of the following activities:
• Product quality complaint, Temperature Excursions or S&L complaint management
• Deviation investigations, quality issue management and escalation
• Product release
• Change control
• SOP management
• Stability Data entry and management
• Supply Chain Assurance (SCA) system administration
• Training System
• Quality Risk Management
• Quality Agreements (establishment and maintenance) between AZ and External Suppliers and between GSQ and AZ Operations Sites.

Key Accountabilities

Complaints Management - Coordinate complaints issued for GSQ as a supplying site or coordinating site
• Product Quality Complaints
• Temperature Excursion
• Supply and Logistics (support when applicable)
• Product security

Supports GSQ Quality Management Systems
• Manages and maintains quality data and records in relevant quality management support systems (GQCLIMS, SAP and OCM) as required.
• SCA data entry and checks
• Stability Data entry and secondary data checks
• Assists in the production of, or contribution to, AZ quality documentation as GSQ SOPs.
• Manages internal deviations in Track wise deviation system.

Product Release - Vaccine products (in accordance with Manufacturing License),
• Batch record reviews (including certificates of analysis/conformance, assessment of deviations as required) including working in relevant quality management systems (SAP, GQCLIMS).
• Assign Usage Decision for batches affected by Critical deviations, assessed by Senior Quality Supplier Manager or Qualified Persons
• Issuance of certificates within GQCLIMS system and manually.

Who are you?
Education, Qualifications, Skills and Experience

Essential

• Bachelor degree in a science / technical field such as Pharmacy, Biology, Chemistry or Engineering (Note: there may be specific additional requirements depending on the regulations in each country). Proven broad experience in either the pharmaceutical operations environment or pharmaceutical Quality Assurance role
• Strong demonstrated knowledge of cGMPs, Quality Systems and the pharmaceutical supply chain environment. Also strong understanding of industry standards such as Pharmacopeia, ISO standards, etc.
• Previous experience of product release role
• Excellent oral and written communication skills [English and local language(s)]

Desirable

• Experience working in a PCO/PET organization or Lean/Six Sigma training.
• Multi-site / multi-functional experience
• Proven experience in Quality Assurance or combination of Quality and Technical
• Strong problem solving skills
• Strong negotiating/influencing skills
• Ability to work independently under his/her own initiative
• Release experience within a Vaccines environment


AstraZeneca är en arbetsgivare som främjar lika rättigheter och möjligheter. AstraZeneca välkomnar ansökningar från alla kvalificerade sökande oberoende av kön, könsöverskridande identitet eller uttryck, etnisk tillhörighet, religion eller annan trosuppfattning, funktionsnedsättning, sexuell läggning och ålder.

Logent är en oberoende tjänsteleverantör inom logistik med ett heltäckande erbjudande inom Supply Chain Management. Vårt erbjudande innefattar tjänster och branschlösningar inom våra tjänsteområden Logistik, Bemanning, Hamn & Hub och Kompetens. Logent finns representerade på ett flertal orter i Sverige och Norge med ca 3000 anställda. Under 2019 omsatte Logent ca 1,5 miljarder SEK.

Vi är måna om våra anställda och erbjuder alla medarbetare försäkringar och marknadsmässiga löner. För dig som vill prova på att arbeta i Norge eller kan tänka dig att arbeta vid någon av de andra orterna där Logent finns representerade i Sverige så har vi på Logent många roliga uppdrag att erbjuda, vi ser gärna att våra anställda utvecklas inom koncernen!

Läs mer på www.logent.se

Varaktighet, arbetstid
Heltid Visstid, 3-6 månader

Ersättning
Fast lön

Så ansöker du
Sista dag att ansöka är 2020-10-15
Klicka på denna länk för att göra din ansökan

Företag
Logent AB

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "2817".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Logent AB (org.nr 556634-4429), http://www.logent.se

Arbetsplats
Logent Bemanning AB

Jobbnummer
5385488

Observera att sista ansökningsdag har passerat.

Prenumerera på jobb från Logent AB

Fyll i din e-postadress för att få e-postnotifiering när det dyker upp fler lediga jobb hos Logent AB: