Validation Expert Packaging – Specjalista ds. Walidacji Pakowania
Stryków (Powiat zgierski) Marketing
Job description
Job Description
In this role you will be responsible mainly for:
- Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging processes and ongoing verification for processes and cleaning (as applicable)
- Support process validation lifecycle activities by ensuring a state of control is maintained through ongoing process verification (OPV). Ensure that appropriate variables are identified for on-going monitoring as a contributor to quality risk management activities
- Author and review process, packaging or cleaning validation protocols & reports, ongoing process and cleaning verification protocols & reports
- Support execution of validation activities at the shop floor
- Support validation lead for KPI reporting
Position Title
Validation Expert Packaging – Specjalista ds. Walidacji Pakowania
Desired profile
Minimum requirements
All candidates interested in this role should present:
- BSc. in Chemistry, Pharmacy, Chemical Engineering or Pharmaceutical
Technology
- Minimum 2-3 year experience in pharmaceutical areas: manufacturing, technology, engineering or QA, relevant to the specialist area of expertise
- Experience in executing process validation
- Expert in reviewing and writing technical reports
- Fluent in English, both verbal and oral and proficient in site local language
- Very good command in MS Office
Job Type
Full Time
Company/Legal Entity
Poland Lek S.A., Strykow
Country
Poland
Work Location
Strykow
Functional Area
Technical Operations
Division
Novartis Technical Operations
Business Unit
NTO SOLIDS
Employment Type
Regular
Sourcing Statement
You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV.