Cleaning Validation Engineer to Alten Pharma

We are now looking for new colleagues who want to work together with us and develop themselves as a consultant in our wonderful Life Science team in the greater Stockholm-Uppsala area!

As a Life Science 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.

You will support our customers in different areas, depending on your experience and interest, for example; quality, validation, process, QC, method development and project management.

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.

 

YOUR DEVELOPMENT

As a consultant, you have a great chance to impact your own development! If you feel that the business is interesting there is a chance to develop into a Business Manager role in time. If the consultant role is more interesting, we have great opportunities to develop into expert roles as well as working in teams and work packages.


THE ROLE:
Prepare Cleaning and Process validation protocols according to internal and external requirements.
Execute qualification, cleaning and process validation tests in accordance with approved protocols, procedures and guidelines.
Analyze cleaning and process validation test data to determine systems have met validation criteria.
Write process and cleaning validation final reports that offer conclusions based on test results.
Document testing results in validation/qualification protocols per protocol requirements; obtain samples to be analyzed per qualification/validation protocol requirements.
Assure that all validation activities are performed in compliance with approved validation/qualification protocols, standard operating procedures (SOPs), and current regulatory requirements/guidelines.
Conduct internal evaluations on the performance and compliance of the Cleaning Validation Program.

 

ESSENTIAL REQUIREMENTS (Education and Experience) 
Minimum of 5 years’ experience in the pharmaceutical/biotech industry and with a thorough knowledge of quality systems, GMP and regulatory requirements including FDA.
At least 3 years’ experience in preforming validation in a GMP environment.
MSc in Chemistry, Pharmacy, Biology or equivalent.
Good team player with strong interpersonal and leadership skills
Practical and enquiring approach to problem solving.
Ability to draw conclusions based on the application of logic and analysis of situations.
Fluent in Swedish and English.

 

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

 

WHAT WE OFFER YOU

Every employee is equally valuable in the success of ALTEN! We are driven by making people grow and develop, which is why we offer you the opportunity to work with what you are truly passionate about. At ALTEN, we have a broad range of assignments at most of the leading companies in Sweden in several different sectors, to make it possible for your wishes to come true. We offer both national and international opportunities and together with your coaching manager, you build your career path so you constantly are able to develop and achieve your goals and dreams!

As a consultant at ALTEN, you will get the genuine team feeling at your assignment but also a wonderful togetherness at ALTEN. Through our different internal networks, such as ALTEN Sports, Women@ALTEN and ALTEN Innovation you will get the opportunity to drive topics and activities that are close to your heart, together with your colleagues. All activities are of course optional. Work life balance is our top priority. We also have a collective agreement and other benefits like Pension, Insurances and Wellness grants.

 

We believe in growing together!