Ardena
Associate Scientist - Analytical Development
Ardena, Sauk Trail Beach, Wisconsin, United States
About us
Ardena
is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalyticalservices.
The
Ardena Group
is operating from five sites in Europe and one in US. For the Ardena branch based in Mariakerke (Gent, Belgium), we are looking for an
ASSOCIATE SCIENTIST – ANALYTICAL DEVELOPMENT WHAT YOU WILL WORK ON Ardena Gent
guides a worldwide portfolio of customers through the processes of formulation and analytical development, the preparation of regulatory dossiers and the manufacturing and labeling of early-phase clinical materials according to GMP appropriate standards.
The analytical laboratory plays a key role in the development and validation of analytical methods to characterize drugs and to perform quality control testing on incoming raw materials and on the finished clinical materials.
YOUR KEY RESPONSIBILITIES
You prepare, perform and report development and quality control analyses according to method descriptions and protocols
You validate analytical methods
You provide active input related to analytical issues
You plan, organize and control the attributed analytical package
You communicate and interact with method developer(s), compliance, Lab management and formulation scientists
You initiate and document investigations and non-conformances
YOUR PROFILE LOOKS LIKE/ RESEMBLES
You have a Bachelor or Master’s degree in science
You have recently graduated or have 1 to 2 years of relevant professional laboratory experience e.g. chromatography (HPLC, UPLC, GC), dissolution, Karl Fisher and spectrometry (UV-VIS, IR)
You are capable of working in a regulated quality control environment (GMP)
You are flexible, a problem solver and a team player
You have an analytical mindset and you are stress resistant
You are fluent in English (written as well as spoken)
You feel comfortable in a dynamic and changing environment
You like to learn and develop yourself
WHAT WE OFFER
An attractive and tailor-made remuneration package including extra-legal benefits such as
Compensation if you come to work by bike
Meal vouchers
Group/hospitalization insurance
Flexible working hours
32 days holiday a year
Ability to grow your skills in a rapidly growing company with international customer portfolio
A dynamic working environment
#J-18808-Ljbffr
is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalyticalservices.
The
Ardena Group
is operating from five sites in Europe and one in US. For the Ardena branch based in Mariakerke (Gent, Belgium), we are looking for an
ASSOCIATE SCIENTIST – ANALYTICAL DEVELOPMENT WHAT YOU WILL WORK ON Ardena Gent
guides a worldwide portfolio of customers through the processes of formulation and analytical development, the preparation of regulatory dossiers and the manufacturing and labeling of early-phase clinical materials according to GMP appropriate standards.
The analytical laboratory plays a key role in the development and validation of analytical methods to characterize drugs and to perform quality control testing on incoming raw materials and on the finished clinical materials.
YOUR KEY RESPONSIBILITIES
You prepare, perform and report development and quality control analyses according to method descriptions and protocols
You validate analytical methods
You provide active input related to analytical issues
You plan, organize and control the attributed analytical package
You communicate and interact with method developer(s), compliance, Lab management and formulation scientists
You initiate and document investigations and non-conformances
YOUR PROFILE LOOKS LIKE/ RESEMBLES
You have a Bachelor or Master’s degree in science
You have recently graduated or have 1 to 2 years of relevant professional laboratory experience e.g. chromatography (HPLC, UPLC, GC), dissolution, Karl Fisher and spectrometry (UV-VIS, IR)
You are capable of working in a regulated quality control environment (GMP)
You are flexible, a problem solver and a team player
You have an analytical mindset and you are stress resistant
You are fluent in English (written as well as spoken)
You feel comfortable in a dynamic and changing environment
You like to learn and develop yourself
WHAT WE OFFER
An attractive and tailor-made remuneration package including extra-legal benefits such as
Compensation if you come to work by bike
Meal vouchers
Group/hospitalization insurance
Flexible working hours
32 days holiday a year
Ability to grow your skills in a rapidly growing company with international customer portfolio
A dynamic working environment
#J-18808-Ljbffr