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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 sens of ethic and a true comitment 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 a Head of Study Director Group, effectively managing a team of toxicology scientists.
Responsible of the overall performance of General Toxicology, Safety Pharmacology and DART Study Directors in line with overall company strategy.

Provides sound multi-disciplinary experience on Toxicology (i.e., subchronic/chronic testing, reproductive/developmental testing, immunotoxicology, toxicokinetics).

Provides leadership and direction to the Study Directors in order to ensure high quality and high standards of work, to meet sponsor requirements in a timely manner and deliver planned operational performance.  

Maintains awareness of current scientific/technical aspects and regulatory requirements of work undertaken in the department. Ensures the up-dating of scientific validity and compliance to national and international guidelines in order to be a referee for internal scientific staff and for the client.
Ensures that all aspects of the studies are performed in compliance with applicable Good Laboratory Practice regulations, company Standard Operating Procedures and in compliance with relevant Health, Environmental and Safety legislation.

Qualification
  • At least ten years of related experience in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
  • Proven effective management and leadership skills
  • History of successful problem solving
  • Strong communication and interpersonal skills
  • 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, 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.
Location:
  • Pomezia (Rome) – Italy
For questions in relation to this job opportunity, please feel free to contact:

Silvana VENTURELLA Scientific & Operational Director, ERT, ERBC Group
Phone and Mobile: +39 06 91095 558 / +39 335 5956972
sventurella@erbc-group.com

ERBC is looking for a Study Director in Developmental And Reproductive Toxicology (DART), including Embryo-fetal Development, Fertility, Pre-/Postnatal and Juvenile Toxicology Studies.

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 Study Director performs, reviews and confirms external, visceral and skeletal fetal abnormalities.

The candidate must be an expert in one or more of the following: fetal pathology, endocrinology, behavioral toxicity/neurotoxicity, juvenile toxicity.

The position requires supporting scientifically clients and other scientific/technical staff in the conduct of GLP and non-GLP DART 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 five years of related experience in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
  • Skilled in performing scientific presentations and preparing scientific publications.
  • 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, 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
For questions in relation to this job opportunity, please feel free to contact:

Silvana VENTURELLA Scientific & Operational Director, ERT, ERBC Group
Phone and Mobile: +39 06 91095 558 / +39 335 5956972
sventurella@erbc-group.com

ERBC is looking for QA auditor in GLP activities.
The Quality Assurance Auditor has overall responsibility for the conduct of audits in accordance with GLP regulation: performing audits of raw data, reports and audit of routine processes to assure compliance with applicable GLP regulatory requirements, and procedures.

Qualification
  • At least two years auditing experience in GLP (or GMP) QA role in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
Education
  • Bachelor’s degree or equivalent, preferably in a life science or related discipline.
Skills
  • Scientific competences in the fields of Toxicology and/or Pharmacology and/or Laboratory Sciences.
  • Knowledge of GLP (or GMP) regulations.
  • Computer system validation Data Integrity.
  • Excellent writing skills.
  • Must be able to clearly write, read, speak and understand scientific and technical English.
Location:
  • Baugy - France
For questions in relation to this job opportunity, please feel free to contact:

Sylvie BIDOLI-BEUTIN Chief officer, Global Quality & Compliance, ERBC Group
sbidoli@erbc-group.com

ERBC is looking for an engineer with experience in process improvement (Lean Six Sigma, 5S, Project management, …), fluent in English, spoken Italian welcome, Lean Six Sigma green and/or black belt certification wished.
The position is based in Pomezia, 25 km south of Rome, Italy (if you are French a V.I.E. contract is possible). Regular trips are to be expected to the group's headquarters in Baugy (18800) France. The successful candidate will report directly to the Director of the Pomezia site and as such will be a member of the Pomezia site management committee, and functionally to the Group Chief Scientific Officer in charge of the continuous improvement of the Group.

Job description
  • Management of projects for continuous improvement of digital processes: is the priority of the position for the year 2021.
  • Management of projects for continuous improvement of business processes (experience in activities in analytical, toxicology and pharmacology laboratories is not required).
  • Management of IS validation processes in a GLP environment according to OECD Guideline 17.
Qualification

Three years in a similar position would be an asset. Freshly graduated engineering student can apply.

Education

Master of Engineering Degree (INSA or equivalent).

Skills

A strong leadership personality is required to support the operational staff in the execution of their improvement plans (i.e. ability to influence and impact, strong results orientation, good ability to communicate clearly with empathy, respect of deadlines).

Location
  • Pomezia (Rome) – Italy
For questions in relation to this job opportunity, please feel free to contact:

Silvana VENTURELLA Scientific & Operational Director, ERT, ERBC Group
Phone and Mobile: +39 06 91095 558 / +39 335 5956972
sventurella@erbc-group.com

Pascal CHAMPÉROUX Chief Scientific Officer, Process Efficiency & Innovation, ERBC Group
Phone:+ 33 (0)2 48 23 00 23
pchamperoux@erbc-group.com

ERBC is looking for an Information Technology specialist with technical expertise and a passion for delivering excellent IT support to a very high standard.

The ideal candidate:
  • Has at least 5 years’ experience working within the IT industry and has a thrust for technology.
  • Is IT literate with strong Microsoft Office skills, especially Excel and Access.
  • Has proven knowledge of database management.
  • Has experience in working with Microsoft Windows & Server and tools such as Active Directory, DHCP, DNS etc.
  • Is able to monitor the network, servers and systems and has the ability to diagnose and resolve basic technical issues.
  • Is familiar with backup and recovery software and methodologies.
  • Has notions of virtual machine management.
  • Has good knowledge of printer fleet management.
  • Has notions of support ticketing systems and SLA’s.
  • Has basic knowledge of data arrays and cluster servers.
  • Has notions of GxP and data integrity regulations.
  • Has basic oral and written communication skills in English.
  • Has the ability to work towards deadlines and deliver as part of a team.
  • Is punctual, flexible and with a proactive personality.

Key Responsibilities and requirements:
  • Assist employees with computer problems and answer their questions.
  • Troubleshoot hardware and software issues in person, remotely and via phone.
  • Verify functionality of hardware and software components, also third party.
  • Third-party applications support and administration.
  • Database support and administration.
  • Conduct daily network backup operations.
  • Log issues reported by employees.
  • Direct unresolved issues to the next level of support personnel.
  • Virtual machine management.
  • User accounts, permissions and passwords management.
Location

Pomezia (Rome) – Italy

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

Remo ROMANO Head of IT Italy
rromano@erbc-group.com

ERBC is looking for a reliable Environmental Health and Safety (EHS) Manager for Baugy Facilities (France) to ensure everyone in the company is compliant with health and safety regulations. She/he will also be responsible for establishing policies and standard operating procedures that will create and maintain a safe workplace.
As an EHS manager, she/he must pay excellent attention to detail to identify hazards and unsafe conditions. She/he will also be able to discover opportunities for improving conditions and execute various safety programs and trainings. The ability to communicate guidelines to a multidisciplinary workforce is essential.
The mission is to ensure that all that Baugy Facility meets all legal expectations and actively supports occupational health and safety.

EHS Manager main responsibilities include:
  • Developing and executing health and safety plans in the workplace according to global policies and legal guidelines
  • Preparing and enforcing policies to establish a culture of health and safety
  • Evaluating practices, procedures and facilities to assess risk and adherence to the law

Qualification

  • At least two years of EHS experience in Pharmaceutical or Chemical industries.
Education
  • Bachelors degree in Environmental Safety, Occupational Safety and Health, or related field required; Masters degree desirable.
Skills
  • Extensive knowledge of environmental regulations and policies.
  • Excellent analytical and problem-solving skills.
  • Excellent organizational skills and attention to detail.
  • Proficient in technology and equipment used in environmental inspections.
  • Excellent written and verbal communication skills. Languages: French, English.
  • Must be able to write, read, speak and understand scientific and technical English perfectly.
  • Reading and understanding Italian would be an asset.
Location

Baugy (Bourges) – France.  
Some missions could be conducted in our Facilities in Pomezia (Rome) – Italy.

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

Sylvie BIDOLI-BEUTIN Chief officer, Global Quality & Compliance, ERBC Group
sbidoli@erbc-group.com

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

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