QUALITY CONTROL ANALYST

Job description

ROYAUME-UNI(Haverhill)
du01 novembre 2020au01 novembre 2022(pour24mois)
ETABLISSEMENT :SANOFI-AVENTIS GROUPE
REMUNERATION MENSUELLE :1681€ (indemnité non contractuelle fixée par décret et arrêté, dont le montant peut varier notamment en
fonction de l’évolution du barème de référence, de la localisation de la mission et des cas d’abattements prévus par les textes)

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

We are looking for a candidate for a VIE mission of:

Quality Control Analyst

Job description:

- Sampling and analysis of raw materials, drug substances and drug products
- Ensure stability testing is initiated and completed within the required time frame
- Documenting analytical data and results according to cGMP (current Good Manufacturing Practice)
- Collation of analytical data into release packs
- Review raw data, ensuring all documented results are in accordance with the appropriate product/material specification
- Responsible for first line troubleshooting
- Support the Quality Control function
- Training and support of colleagues
- Support equipment requalifications, calibrations, services etc.
- Carry out Risk/COSHH (the Control of Substances Hazardous to Health Regulations) assessments, ensure that the laboratory is maintained in a safe and tidy manner
- Raise Events, CAPA's ( Corrective and preventive action )& Laboratory investigations immediately
- Identify and implement improvements to ways of working
- Take responsibility for adhering to cGMP requirements during all activities performed
- Works as part of a team, within well-established, defined processes & procedures

Key “MUST HAVE” competencies, skills & experiences

Education:

- Bachelor’s Degree in Life Science (Chemistry, Pharmacy or related field)

Professional experience:

- Working knowledge of laboratory health and safety
- First working experience in Quality Department is preferred
- Knowledge of relevant regulations, guidelines, good practices, sustained competences in analytical techniques and skills applicable to affiliate operations would be a plus
- Experience in a pharmaceutical environment would be a plus

IT / hard skills:

- Demonstrated ability to work consistently to quality policies and cGMP (current Good Manufacturing Practice)
- Good knowledge of Microsoft Office package
- Knowledge of statistical tools would be a plus

Soft skills:

- Demonstrated ability to successfully manage own workload to meet departmental targets
- Act for change
- Strive for results
- Cooperate transversally
- Commit to customers
- Proactive
- Being able to take ownership for actions
- Analytical thinking

Languages:

- Fluent English