Valesta is the privileged partner of pharmaceutical companies, CROs (Contract Research
Organisations) and all other companies that organize, coordinate and carry out clinical
research projects.
To support our ongoing growth and the urgent demand of one of our clients
we are searching for an enthusiastic
QC Development & Stability Expert
Maybe you will be our next colleague?
> Job Description
As a QC Development Expert, you are responsible for the development, qualification and
validation of (analytical) release and stability methods for new developed IVD products and
you make recommendations for the performance of experiments in the area of quality control
(QC).
> Responsibilities
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You plan and perform experiments with a high degree of independence, perform
trending and interpret data in order to draw conclusions. You also write protocols,
report, and transfer documentation on (analytical) test methods and QC
methodologies.
You have a profound understanding of method development, qualification and
validation of (analytical) QC methods including instrument qualification and validation.
You assist in setting up and maintaining stability processes for raw materials as well as
QC test panels.
You apply state-of-the-art knowledge to assigned project(s), you have a high level of
technical proficiency, and modify and introduce new methodologies to improve the
quality, accuracy and usefulness of data
You interface with R&D and Operations organizations to ensure methods and
technology are consistent throughout the company
You lead troubleshooting activities for established test methods used in development
and release testing
You provide support in formulation optimization and process development
You keep abreast of current developments and literature relative to new QC
methodologies and perform literature searches on own initiative.
You present your own work at in-house forums and at professional meetings
You are able to write protocols, reports, technical reviews, transfer documentation
and SOPs autonomously
You follow policies, SOP’s and other applicable guidelines
> Profile
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You have a master degree with 1 - 5 years’ experience in chemistry, biochemistry or
molecular biology in industry, preferably in a medical or diagnostic environment
A PhD is a nice to have
You have a strong knowledge of QC method development and/or stability
You have basic knowledge of clinical sample preparation, DNA/RNA extraction and
real-time PCR
You are able to write protocols, reports, standard operating procedures and test
methods
You are able to interpret data and have strong analytical and problem-solving skills
Knowledge of statistical techniques, such as data trend analysis and design of
experiments and relevant software tools, is highly desirable
You pay attention to detail and you are quality driven
You have excellent oral and written communication skills
You are able to manage multiple priorities
You have the ability to execute effective decision-making, both as an individual and as
part of a team and planning
Your English is perfect (written and spoken)
You have knowledge of relevant software tools (e.g. data analysis)
You are technology-orientated
You are a team player and you are able to work independently
You have good time management skills
You have problem identification, analysis and solving skills
You are results-oriented
You have strong analytical skills
> Company Description
Valesta is a dedicated HR partner for pharmaceutical firms as well as CROs (Contract Research
Organizations) and all other companies that organize, coordinate and carry out clinical trials.
Valesta operates as a matchmaker between companies seeking for the right staffing solution
for ongoing clinical research projects and professionals working in clinical trials looking for a
first or next step in their career.
Next to our expertise (thanks to our years of experience in the field of clinical studies), we
offer a continuous flow of new client requests and career opportunities, ranging from
administration to management, from research to commercial, all situated in the exciting world
of clinical trials.
> Offer
We recruit candidates for contracts of unlimited duration, with great opportunities for
personal growth, all tuned in to your personal needs.
Valesta offers
 A challenging job in an exciting environment
 An attractive salary with additional benefits completely in line with your function and
experience.
> Contact
Are you interested in working with Valesta?
Don’t hesitate and apply as soon as you can!
Send your application letter and CV in English to
[email protected]
Should you have any additional questions, do not hesitate and contact us immediately.