Analytical Specialist within Quality Unit

Job ID:  54966

Location: 

Wien, AT

Job Level:  Professionals

Job Category:  Quality

Employment Type:  Permanent position

Do you want to combine the opportunities that a global company provides with the advantages of a family-owned business? Octapharma is a biotechnology pharmaceutical company with large-scale manufacturing in northwestern Kungsholmen - with a vision to improve people's health and lives.
 

What will you do as an Analytical Specialist?

• Prepare validation documents and other GMP relevant documents with support of senior analytical specialists and team leaders

• Develop and validate methods and support troubleshooting in the QC laboratories

• Support of method development in collaboration with the product specialists at R&D

• Sample administration and follow up of the validation related testing in the QC and R&D laboratories

• Preparing statistical evaluation of data and reporting in Excel

• Support of method transfer and implementation of the methods at the receiving laboratory

• Administrate documents required for submission and support within inspection tasks
   

Your Profile

• University degree (MSc, Phd or equivalent) in chemistry/biosciences

• Work experience in pharmaceutical industry especially in the field of method validation (GMP environment) is a plus

• Willingness to travel due to business trips

• Good knowledge in MS Word and MS Excel

• Excellent English communication skills (oral and written), Swedish or German is a plus

• Social skills and presentation skills

• Strong problem solving, organizational and time management skill

• Ability to multitask and a high level of flexibility

Corporate QC within Quality Unit

• Overall responsibility for quality control and quality assurance of our medicines

• Regulatory compliance and quality assurance for comprehensive systems

• Manufacture of biological medicines entails extra high quality requirements

• Works together with other functions related to everything from the blood plasma we use as raw material to the final release of the finished product to our patients

• The department corporate QC Method Validation (cQCMV) consists of 27 people and is distributed between several Octapharma sites
   

What is the best thing about working with us?

• You contribute to saving lives - Every day is meaningful as we manufacture life-saving medicines

• Benefits – Bonus program, benefits portal with advantageous deals and offers as well as naprapat at the workplace and more.

• Family values ​​- Long-term perspective regarding personnel and relationships

• Bistro bryggeriet – Homemade food is served every day and we have our own bakery/café

• Historic and unique work environment – ​​State-of-the-art offices originating from Stora Bryggeriet (a beer brewery from 1892)

• Competence development - We offer, among other things, several different employee and leadership training courses, both internal and external, trainee programs and digital solutions
   

Apply today!

If you have questions about the position, contact Tina Eriksson Heyder at 0760004308. Application deadline is 2023-03-21, the position can be filled before then.
 

If you go further in the process

• We want to collect as much information as possible early in the process to be able to make the best match

• Within a few days, you will be able to carry out occupational psychology tests

• The tests are done early in the process because we want to ensure an objective, unbiased and fair selection process

Do you want to get to know us better? Learn more about Quality Unit on our website and follow us day by day on LinkedIn! 
 

Union representatives
Unionen, Zahra Kafash-Hoshyar, 08-566 433 13
Akademikerföreningen, Ann-Charlotte Hinz, 08-566 431 35