המקום בו המומחים והחברות הטובות ביותר נפגשים
Key Responsibilities:
This role is based on a 2 shift cycle - Day shift 6am – 2pm & Evening shift 2pm – 10pm
Are you?
Degree level educated within a scientific discipline
Do you have?
Knowledge of cGMP, and GMP for Labs requirements.
Broad Knowledge of Analytical Techniques and Experience in HPLC/UPLC
People management experience
Experience in Calibration Systems
Operation of Laboratory Instruments skills
Experience of Chemicals and Associated Dangers
Knowledge of Company Policies, Procedures and Quality Systems
cGMP Regulatory Bodies Experience
Knowledge & Understanding of the Chemical / Pharmaceutical Manufacturing sector
Familiarity with US and European regulatory guidelines.
Documentation Compliance experience
Report Writing / Technical Report writing skills
Computer Systems Validation & GMP Guidelines
Interviewing skills
Opex mindset to drive and improve performance in QC
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Internal Eligibility for Job Postings
Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:
Be a current employee of Teva
Meet the basic requirements for the job
Have received a rating not lower than “Successful” on their most recent performance review and must not currently be on a performance improvement plan
Apply to the posted requisition within the allotted time frame
Have been in their current position for a minimum tenure of twelve (12) months
Unless explicitly stated in the job description, no company sponsored work authorisation no relocation assistance should be assumed.
משרות נוספות שיכולות לעניין אותך