Mass Spectrometry Lab Technician – Sophia Antipolis

Description

Mass Spectrometry Lab Technician

Translational Sciences Lab Technician – LC-MS/MS (TECHNICIEN(NE) EN BIOANALYSE)

Le(La) Technicien(ne) en Bioanalyse est responsable d’extraire et d’analyser les échantillons par chromatographie liquide couplée à la spectrométrie de masse, conformément aux procédures et aux MON (Modes Opératoires Normalisés) établis. Il/Elle travaille dans un environnement réglementé et dans le respect des délais. 

ROLE ET RESPONSABILITES (scroll down for the english text)

• Effectue toutes les activités liées au traitement des échantillons (précipitation de protéines, extraction liquide-liquide, extraction en phase solide) permettant d’extraire la molécule, l’entité d’intérêt à quantifier.
• Documente les activités relatives à l’analyse d’échantillons selon les bonnes pratiques de laboratoire et aide à la vérification de divers documents.
• Participe à la révision de MON en bioanalyse.
• Réalise les séries d’analyses de petites molécules à l’aide des instruments et du logiciel approprié (LIMS Watson, LC-MS/MS via Masslynx, Analyst).
• Participe à l’élimination des déchets chimiques et biologiques produits par les employés de laboratoire et aide au nettoyage de l’équipement et des instruments de laboratoire.
• Effectue des tâches de soutien afin de répondre aux besoins des utilisateurs du laboratoire.
• Effectue les activités conformément aux politiques, aux Modes Opératoires Normalisés et aux guides d’opération en vigueur de l’entreprise et de la division, effectue d’autres tâches assignées par la direction.

Job responsibilities 

• Conduct experiments and analyses related to studies from the relative platform. You will perform analyses such as the quantification of small molecules
• Perform all activities related to the extraction (protein precipitation, liquid-liquid extraction, solid phase extraction) and the analysis of biological samples by liquid chromatography coupled to mass spectrometry.
• Document the sample analysis activities performed according to the good documentation practices and contribute to the verification of the documentation 
• Contribute to the revision of the controlled documents
• Perform the assays to analyze small molecules using appropriate instrumentation and software (LIMS Watson, LC-MS/MS via Masslynx, Analyst)
• Contribute to the lab functioning: disposal of biological and chemical wastes, cleaning of instrumentation 
• Perform all the activities in agreement with the current regulations, the controlled documents and user guide applicable within Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. 

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know: 

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. 
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Qualifications

What we’re looking for

• Bac+ 2/3 DUT – BTS – DEUST degree in Science or an equivalent combination of education, training and experience. 
• Relative alternate certification may be considered acceptable.
• Experience in regulatory context will be considered an asset
• Experience within a client-service environment, either in a contract laboratory or within a core group at a pharmaceutical company. 
• In-depth understanding and knowledge of the pharmaceutical industry and contract research organizations in general, and the preclinical community specifically
• Customer oriented, service oriented, and open to learn new skills
• English level: Required English proficiency includes being able to communicate verbally on subjects that are frequently specialized and technical, and writing complex technical reports. 

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health

Additional Information:

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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