Quality Assurance Engineer to company working with industrial gases!

Quality Assurance Engineer to company working with industrial gases!

Arbetsbeskrivning

We are looking for you who is attracted by the idea of working for a good cause that will affect the patient safety. In this position as a Quality Assurance Engineer, you will develop the idea of quality as a tool for patient safety. The organization is well-known within the industry and they are eager to hear from you who is looking forward to using your previous knowledge and be a crucial part in the working chain. You will be responsible for several areas within the quality spectra, you will for example make sure that personnel are trained, you will be responsible for approving subcontracted activities which may impact on GMP and much more. If this sounds like your next challenge, apply today! We look forward to receive your application!

OM TJÄNSTEN
As a Quality Assurance Engineer you will contribute to further upgrading to a Pharmaceutical Gas Company cross-functional co-operation. You will be working with releasing raw materials, intermediates and finished medical gases and special medical gases according to specifications & GMP. Furthermore, you will ensure quality systems are implemented and maintained. Lastly, you will work both self sufficiently and with others and be socially stimulated in your daily work.

You are offered

• A position that is allowing you to use your previous experience, but it also gives you the opportunity to learn in a new working environment

• An employer that is in an expansive phase

• A position that is centered around questions regarding GMP, GDP, ISO etc.

As a consultant at Academic Work you are offered a great opportunity to grow as a professional, extend your network and establish valuable contacts for the future.

ARBETSUPPGIFTER
• Approve validation and qualifications

• Work with batch documentation and make sure it’s correct

• Ensuring customer complaints are dealt with effectively

• Ensuring internal audit program in place and be part of audit team

• Deciding on the final disposition of returned, rejected, recalled or falsified products

VI SÖKER DIG SOM
• A candidate who is fluent in Swedish and English, both verbal and written as you will use both languages daily

• A candidate who possess a University degree in Pharmacy, Chemistry or similar

• At least 2 years experience from a similar position where you have earned good knowledge in Quality Management, Eu pharmaceutical legislation, ISO, GMP, GDP and Medical Device Directive. This has to be clear in your application.

As a person you are:

• A good communicator

• Structured

• Result oriented

Other information


* Start: As soon as possible, we consider applicants with 1 months’ notice period at the most
* Work extent: Full time
* Location: Enköping
* Contact information: This recruitment process is conducted by Academic Work. It is a request from our client that all questions regarding the position are handled by
Academic Work.


Our selection process is continuous and the advert may close before the recruitment process is completed if we have moved forward to the screening or interview phase.

Kontaktpersoner på detta företaget

Sara Frykedal

Consultant Manager Fanny Rosén
08-52257636
Fanny Rosén

Mette Risberg
0736448575
Hedvig Svärd

Konsultchef Catrin Laudon

Sara Frykedal
08-52257605
Fredrik Bardon

Konsultchefsassisten Anna Bengtsson
08-12 05 2224
Konsultchef Lisa Nordell
0812052231

Sammanfattning

  • Arbetsplats: Academic Work
  • 1 plats
  • 6 månader eller längre
  • Heltid
  • Fast månads- vecko- eller timlön
  • Publicerat: 24 november 2020
  • Ansök senast: 24 december 2020

Besöksadress

Lindstedtsvägen 24
Stockholm

Postadress

Lindstedtsvägen 24
Stockholm, 11428

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