QA Specialist / Pharma / nearby Zwolle / Production / GMP / Audits

Bedrijfsnaam: -
Plaatsingsdatum: 25/02/2019
Standplaats: -


SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical, Chemicals and Biotechnology organisation, based in Overijssel Netherlands.The CompanyOur client is an international company that is responsible for the filling of Lactulose, the production of hormone preparations and the formulation of Mebeverine. For these products our client is the center of excellence. They are looking for a motivated and passionate candidate, with a hand-on mentality, who strives for quality in importance for the workplace and organization.

Are you the one? Read more!

Role DescriptionAs a Production Quality Specialist you come to work in a team together with other Production Quality Specialists and Engineers. As Production Quality Specialist you work within the Solid Production department and report to the Head of Manufacturing Solid Products of our client. You work closely with colleagues from production and the various quality departments.

What if you are selected?

If you are the one the are searching for you will be responsible for ensuring the quality of produced batches based on GMP and internal standards. You will keep an overview of the review of batch documentation and you conduct more complex deviation studies. You have a leading role during (inter) national audits of clients and governments. Exciting don't you think?

ResponsibilitiesMany responsibilities, a varied range of duties and a leading role! What else do you wish for?

The following tasks are you responsibilities, like i said, 'a varied range of duties' is waiting for you:
You will be the end-responsible for reviewing and approving produced batches, also you will be responsible for the quality of produced batches of various products. An other task is the conduct research, reporting and processing of deviations and CAPA's to improve quality. You are responsible for continuous process verification (CPV) reporting and optimization. Also are you responsible for the implementation and compliance in accordance with the requirements of the applicable quality assurance systems (GMP, ISO).

Lean back, it's allot.. But it may be also yours life changing moment!

RequirementsThe most important part; Do you have what it takes?

Our client is looking for someone with the following skills, knowledge and experience:
- You need to have a MSc. Pharmacy, Life Sciences, Chemical or Food Technology (or higher);
- You need to have minimal 2 years work experience within the pharmaceutical industry;
- You have experience with audits and inspections;
- You are excellent in the Dutch and English language (word and writing);
- GMP is known to you and working according to guidelines is a 'piece of cake'

Other informationSo... Are you the one? Apply!

"It always seems impossible until it is done" - Nelson Mandela

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :