Cette offre d'emploi n'est plus disponible
À propos
Read all the information about this opportunity carefully, then use the application button below to send your CV and application.
The testing carried out is on In coming materials.
Actively involved in Investigations Always ensure compliance with EHS, actively participate in EHS activities and 5s.
Perform routine instrument calibration checks at appropriate times.
Preparation and control of Standard Operating Procedures and always ensuring compliance with cGMP guidelines.
Completion of Documentation for Batch Release process.
Assisting in the provision of trends Assist in audits.
Generation/ reporting of Key performance indicators for the group.
Ensure compliance with current pharmacopoeias and all regulatory/company guidelines.
Interaction with other departments e.g., QA, BU, Sterility assurance etc.
Keep colleagues informed of current issues and developments as appropriate.
Reasonable level of overtime will be required to facilitate the business needs.
Carry out additional duties as deemed necessary by your PTL/Senior Analyst PRINCIPAL QUALIFICATIONS: A third level Science Qualification Skills REQUIRED: Good communications skills, excellent time management skills, flexibility and agility will be required.
Openness to change.
Proven ability to work on own initiative and deliver expectations.
DESIRED WORK EXPERIENCE: Pharmaceutical experience in a GMP regulated laboratory environment.
Additional Information Relocation Assistance Provided: No To be considered for this role you will be redirected to and must complete the application process on our careers page. xyswxtq
To start the process, click the Apply button below to Login/Register.
TPBN1_IJ
Compétences linguistiques
- English
Avis aux utilisateurs
Cette offre a été publiée par l’un de nos partenaires. Vous pouvez consulter l’offre originale ici.