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Data Reviewer and QC Documentation Specialist

Date: Jan 12, 2022

Location: Rho, IT, 0000

Company: Teva Pharmaceuticals

Who we are

 

Teva, world leader with over 40.000 employees, in the field of equivalent medicines, with a differentiated business that also includes specialist medicines, over-the-counter drugs and the production and marketing of APIs (active pharmaceutical ingredients), is present in Italy for over 25 years with a commercial branch and manufacturing sites.
Our mission is simple: improve the wellbeing of our patients.
We care about them and about our colleagues, creating a respectful, diverse and inclusive working environment, committing ourselves to maintaining high standards of quality, compliance and safety, always respecting our values (Teva Code of conduct).
We all work for one company and we work together to achieve a common goal.
 

Reporting to

 

QC Coordinator

Main activities and responsibilities

 

•Reviews the analytical data by signing the Analytical sheets or Laboratory notebooks and the electronic reports, where applicable. 
•Performs the periodical review of Audit Trails.
•Supports the revision and creation of QC documentation, such as monographs, analytical sheets, SOPs and Excel worksheets.
•Approves in the LIMS system raw materials, IPCs and intermediates, as a back-up of the QC Supervisors.
•Updates the QC documents in accordance with the pharmacopoeia changes (SOPs, test methods, specifications).
•Provides support for Laboratory investigations, OOS or OOT and manages the relevant TW records.
•Organizes the shipment of samples for external analyses.
•Supports the QC Supervisors and QCM throughout the conduction of internal and external audits.
•In the fulfillment of all the aforementioned tasks, upholds the internal procedures, guidelines and policies.
 

Requirement

 


•Solid scientific and technical background
•Preferential title: university degree
•Previous experience working in a QC laboratory environment operating to GMP principles.
•Knowledge of the GMP regulations relevant to API manufacture.
•Ability to multi-task, prioritize and manage time effectively.

What we offer

 

We try to take care of our employees, offering them small and large benefits. By way of example:
•Recognition Program
•Health insurance
•Canteen
•Coffee Key
•Welfare platform

 

Type of contract: permanent

Department

Location and working program

 

Rho (MI) site, from Monday to Friday (for production reasons, attendance on two shifts may be required).

Teva’s commitment to equal opportunities

 

Teva is committed to equal opportunities in the world of work. Our global policy requires equal employment opportunities to be provided regardless of age, race, religion, health, identity or gender expression, or any other legally recognized status that is entitled to protection under applicable laws.