Validation Engineer

Publiceringsdatum: 2024-03-08

Funderar du på att söka jobb inom yrken med teknisk inriktning? Ett spännande jobb som civilingenjör, kemi hos Alten Sverige AB väntar på dig - varför inte söka idag? Vill du arbeta heltid hos Alten Sverige AB? Just nu letar de efter någon som vill ha en tjänst tills vidare.

Denna position är tillgänglig i Stockholm. Alten Sverige AB söker för närvarande efter en person att anställa inom civilingenjör, kemi-branschen. Ta en titt på deras lediga tjänst för att se om något av dem passar just dig. Här är chansen att bli en del av Alten Sverige AB och jobba som civilingenjör, kemi! Ansök senast onsdag den åttonde maj 2024.

Jobbannons

WE ARE NOW LOOKING FOR NEW COLLEAGUES WHO WANT TO WORK TOGETHER WITH US AND DEVELOP THEMSELVES AS A VALIDATION CONSULTANT IN OUR LIFE SCIENCE TEAM IN THE GREATER STOCKHOLM-REGION!

As a Validation consultant in ALTEN, you work with different interesting customers that we support in the Pharmaceutical Industry. We aim to make a difference for our clients as well as their end users, the patients! Our clients and colleagues are located in Stockholm, Uppsala, Södertälje and Strängnäs.

As a person, it is important that you are flexible, driven, accurate, efficient, helpful and structured while being social and a team player. You must be able to plan, prioritize and perform your tasks independently and in a solution-oriented way.

As a consultant, you have a great chance to impact your own development! Once you get some seniority we have great opportunities to develop you into expert roles as well as working in teams and work packages.

THE ROLE

Lead, plan, coordinate and/or perform validation and qualification

Perform qualification and validation test of equipment, process, method, system, and/or instruments

Issue and review validation plans, protocols and reports

Investigate deviations and follow up with CAPA

Define manufacturing processes, equipment, method, system, and/or instruments

Create or support the creation of URS

Define, write, review, update validation documentation, perform validation activities, such as validation assessments, validation plans, FAT&SAT protocols, IQOQPQ protocols and reports

Risk analysis and management

Initiate and manage change management operations

ESSENTIAL REQUIREMENTS  (Education and Experience)

At least Bachelor degree in a relevant science/technical field; e.g. Pharmacy, Biology, Chemistry or Engineering

At least 2 years of experience with validation and/or qualification within the pharmaceutical industry

Ability to demonstrate knowledge in GxP

Ability to work independently under your own initiative

Good communication and presentation skills

Problem solving skills

Fluent in Swedish and English in both written and speech

VALUBLE QUALIFICATION AND EXPERIENCE

Knowledge in SAP, LIMS

Knowledge of automation, CSV, 21CFR11 and GAMP5

Cleaning validation (CV) and/or work in clean rooms

Sterilization and Aseptic experience

Good experience of Change Control

Qualification of process equipment, packaging or analytical instruments IQ/OQ/PQ,

Excellent knowledge of interpretation of the demands in Eudralex and FDA.

ABOUT ALTEN:

ALTEN is one of Europe’s largest consulting companies within Engineering, IT and Life Sciences with over 54,000 employees in more than 30 countries. We’re a global actor with a local presence with 1400 committed colleagues in offices from Lund in the south to Skellefteå in the north. Our engineers carry out complex and highly technical projects throughout the product development chain of the most prestigious companies in sectors such as Automotive, Aerospace & Defense, Energy, Manufacturing, Public Sector and Life Sciences.

For four years in a row, ALTEN has been named one of Sweden's most attractive employers by Karriärföretagen, an award for employers that offer unique career and development opportunities.

Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you!

BUILDING TOMORROW'S FUTURE TODAY!