QA Officer / Pharma / region Amsterdam / GMP (FDA)
Location: NetherlandsSIRE® 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 Zuid-Holland Netherlands.
Our client is looking for a QA Officer for the Quality Assurance department. Someone who wish to enhance their own development!
- Participate in project teams as QA project lead and contact person for clients
- Batch release preparation
- Coordination and maintenance of quality management systems
- Handling and assessment of deviations and change controls
- Participate in project teams as QA project lead and contact person for clients
- Execution of internal audits according to audit plan and support during external audits (clients and governmental bodies)
- Minimum of HBO educational level in the orientation of Chemistry, (Micro)Biology or Pharmaceutical Sciences
- Profound knowledge of Dutch and English language, verbal and written
- Ability to work with tight deadlines and handle multiple tasks
- A minimum of 4 years experience in the pharmaceutical industry
- Excellent verbal and written communication skills
- Computer fluency in MS-Office, e.g. Word, Excel, PowerPoint; knowledge of TrackWise is a plus
- Experience with FDA compliance is a plus
Are you the one they are looking for? Our client offers you exciting work as part of a team of experts who treat each other as equals.
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.
The Company
As one of the world’s most research-intensive chemical companies, our client have been developing leading solutions for numerous sectors. Our client is a fast-growing company, and the are looking to attract motivated new colleagues who share their values and who would like to be part of their family.Our client is looking for a QA Officer for the Quality Assurance department. Someone who wish to enhance their own development!
Role Description
As a QA Officer you will be doing typical QA tasks; like reviewing and approving the GMP documents and master batch records. Reviewing and approving of batch manufacturing and QC testing records. Sound interesting? Discover more of your responsibilities!Responsibilities
More of your responsibilities as QA at our client will be:- Participate in project teams as QA project lead and contact person for clients
- Batch release preparation
- Coordination and maintenance of quality management systems
- Handling and assessment of deviations and change controls
- Participate in project teams as QA project lead and contact person for clients
- Execution of internal audits according to audit plan and support during external audits (clients and governmental bodies)
Requirements
Check the requirements, see yourself in it? Don't hesitate and apply!- Minimum of HBO educational level in the orientation of Chemistry, (Micro)Biology or Pharmaceutical Sciences
- Profound knowledge of Dutch and English language, verbal and written
- Ability to work with tight deadlines and handle multiple tasks
- A minimum of 4 years experience in the pharmaceutical industry
- Excellent verbal and written communication skills
Other information
Do you own these extras?- Computer fluency in MS-Office, e.g. Word, Excel, PowerPoint; knowledge of TrackWise is a plus
- Experience with FDA compliance is a plus
Are you the one they are looking for? Our client offers you exciting work as part of a team of experts who treat each other as equals.
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.
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