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ERBC is a fast growing non clinical service provider with facilities in Italy and France and offers exposure to a wide variety of study designs. Opportunities to tackle scientific and technical challenges are numerous and stimulate curiosity and engagement. ERBC is an open-minded organization offering personal development opportunities.

At ERBC group, we value our employees and consider them an integral part of our company’s growth and success. Our employees are our most valuable asset, and the individual perspectives and contributions of each person on our team are essential to our success. When recruiting, we are looking for people who have expertise, team-spirit, great sense of ethic and a true commitment in animal welfare. We commit to the creation of a durable relationship with our employees by ensuring that their working environment fosters team spirit, promotes training and offers career development opportunities in France and in Italy.
 
By joining ERBC group, you will join an entrepreneurial project with a human dimension that values individual and collective responsibility, with a high societal dimension and the ambition to contribute to the progress of medical research.

 

Interested in joining our team?

Discover here our currently open positions – if there is any - and send our HR team your application by completing the form below.

ERBC is looking for an in vivo toxicology technician to join its team in Baugy (close to Bourges), France (See job description in French).

The in vivo Toxicology Technician is responsible for performing accurate, high quality in-life study work for toxicology studies, apply all procedures (treatments, clinical observations, blood sampling, etc) in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and according to the Study Director and the study coordinator recommendations. As a polyvalent technician, you will work on several rodent and non-rodent species and for different kinds of studies.

You will also be responsible of creating, maintaining and finalizing raw data files, guaranteeing the quality of data produced. You will have to work in complete transparency with the Study Director and the study coordinator, maintaining a climate of trust with the quality assurance unit. You will have to participate in ensuring that work areas are kept clean and orderly, check that the animals in the facilities are in good health and ask for a veterinarian assistance when necessary.

As an in vivo technician, you will work during some week-ends and may exceptionally work by night.

 

Qualification
  • At least three years of experience as an in vivo technician
  • Experience working in an environment with high quality standards (such as GLP, ISO...) and established testing facility operations and procedures.
Education
  • IUT, BTS or licence in biology, veterinary technology, or related field.
Skills
  • Strong organizational and time management skills, ability to handle multiple projects simultaneously while maintaining data quality and meeting timelines.
  • Ability to work effectively in a collaborative, team oriented environment and to meet study timelines.
  • Excellent use of electronic data capture systems, spreadsheet applications or other data management system.
  • Must be able to read and understand scientific and technical English perfectly.
Location
  • Baugy (Bourges) – France. 
For questions in relation to this job opportunity, please feel free to contact:

Marie WEINZAEPFEL, Head of In vivo Toxicology & Pharmacology, ERBC Group mweinzaepfel@erbc-group.com

ERBC is looking for an enthusiastic Study Director of in vivo Toxicology or Pharmacology Studies at its Baugy site, near Bourges (France).

As a scientific project leader, the Study Director has responsibility for the execution of nonclinical toxicology studies. In line with client requirements, he/she will manage the conduct of GLP and non-GLP in vivo toxicology studies in rodent and non-rodent species, including study design development, managing the team execution of the study, collecting, analyzing and interpreting study data and writing scientific study reports.

The Study Director ensures documentation and execution of the study in compliance with internal procedures and in alignement with any quality standards by collaborating with support functions (quality assurance, documentation…).

He/She will contribute to the department scientific and technical improvements in collaboration with his/her peers and other internal scientific and technical staff by developing and sharing his/her own expertise.

ERBC is a fast growing non clinical service provider with facilities in Italy and France and offers exposure to a wide variety of study designs. Opportunities to tackle scientific and technical challenges are numerous and stimulate curiosity and engagement. ERBC is an open-minded organization offering personal development opportunities.


Qualification
  • If possible, at least two years of experience in managing experimental life science studies in Contract Research, Pharmaceutical, Chemical or Biotechnology Organizations.
  • Developed technical expertise in a field relating to testing of ingredients or devices (toxicology, pharmacology, pharmacokinetics…, in vivo preferably, or in vitro).
  • Experience of internal or external client management through result presentation and discussions based on scientific reports and/or publications.
  • Experience in working in an environment with high quality standards (such as GLP, ISO...) and established testing facility operations and procedures.

Education
  • PhD, Pharm D., DVM or equivalent.
Skills
  • Excellent technical writing and computer software skills.
  • Leadership skills for managing multidisciplinary teams for conduction of studies or projects.
  • This position requires ability to speak, write, and read English.

Location

Baugy (Bourges) – France.

Reference: BAU001TOX


For questions in relation to this job opportunity, please feel free to contact:

Stéphanie FLOURAC: Chief Human  Resources Officer, ERBC Group
hr@erbc-group.com

ERBC is looking for a Study Director for General Toxicology Studies in rodents and non-rodents species in Pomezia.

The Study Director has overall responsibility for the conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results.

The position requires supporting scientifically clients and other scientific/technical staff in the conduct of GLP and non-GLP toxicology studies, including study design development, managing the execution of study conduct, collecting, analyzing and interpreting data, utilization of technology and study report writing.

Qualification
  • At least two years of related experience in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
  • Strong working knowledge of AAALAC and GLP regulations and preclinical testing facility operations and procedures.
  • Experience of client management and technical expertise in the relevant business line.
Education
  • PhD or Master Degree in Biological Sciences, Pharm D., DVM or related discipline.
Skills
  • Excellent technical writing and computer software skills.
  • Must be able to clearly speak, write, read, and understand English.
  • Leadership skills for managing multidisciplinary teams for the conduct of studies or projects.
Location

Pomezia (Rome) – Italy

Reference : POM001TOX

For questions in relation to this job opportunity, please feel free to contact:

Stéphanie FLOURAC: Chief Human  Resources Officer, ERBC Group
hr@erbc-group.com

ERBC is looking for a Study Director in validation of Analytical and Bioanalytical methods at its Pomezia site, near Rome (Italy).
The Study Director has overall responsibility for the conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results.


The candidate must be an expert in one or more of the following techniques: HPLC/UPLC, GC/GC-MS, LC-MS/MS.
The position requires supporting scientifically clients and other scientific/technical staff in the conduct of GLP and non-GLP Analytical and Bioanalytical studies, including study design development, managing the execution of study conduct, collecting, analyzing and interpreting data, utilization of technology and study report writing.

Qualification
  • At least two years of related experience in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
  • Strong working knowledge of GLP regulations and their applicability in analytical and bioanalytical methods development.
  • Experience of client management and high technical expertise in the relevant business line.
Education
  • PhD, Chem D. or related discipline.
Skill
  • Excellent technical writing and computer software skills.
  • Must be able to clearly speak, write, read, and understand English.
  • Leadership skills for managing multidisciplinary teams for the conduct of studies or projects.

Location

Pomezia (Rome) – Italy.

Reference: POM001CHEM

For questions in relation to this job opportunity, please feel free to contact:

Stéphanie FLOURAC: Chief Human  Resources Officer, ERBC Group
hr@erbc-group.com

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