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Senior QA Compliance Expert
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client
Projektbeschreibung
For our client in Stein we are looking for a Senior QA Compliance Expert for a 6 month contract.
Place: Stein
Duration: ASAP-31.12.2017
Workload: 100%
Job Purpose:
To plan and execute assigned GMP QA Compliance tasks related to the support of sterile manufacturing, such as: supporting qualification and validation activities related to routine manufacturing and launch projects, review and approval of GMP relevant documentation, Change Control, Deviation handling and representation of QA Compliance Qualification & Validation in dedicated project(s).
Major accountabilities:
Represent QA Compliance Qualification
Erfahrung: Professional experience in Quality Control/Quality Assurance or in the manufacturing of pharmaceutical drug products and Steriles/Biotechnology
Profound knowledge of cGMPs
Technical/Professional Knowledge and Skills
Knowledge of the current pharmacopoeia requirements including technical methods (USP, Ph. Eur, JP,Coaches and inspires people to achieve team goals
Superior problem solving, decision making and planning skills as appropriate.
Sets clear priorities for task for him/herself and the team.
Excellent knowledge of GMP regulations
Ability to work under time pressure
Focus on customer satisfaction
Recognized expert; networking with CPL/QA/QC, PUs, TRD, HSE, RegCMC, SCM, etc.
Support PUs to guarantee high quality and current GMP
Provides new solutions for existing processes and is committed to continuous improvements
Assumes responsibility and sets clear priorities
Is a strong team player
Readily shares information and professional knowledge
Is a role model
Communicates on all levels within and outside own function
Works independently, efficiently and contentiously
Is committed to quality, GSU and GMP
Is goal-oriented and flexible
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) (see below) For further details feel free to call me
I am looking forward to receiving your application.
Place: Stein
Duration: ASAP-31.12.2017
Workload: 100%
Job Purpose:
To plan and execute assigned GMP QA Compliance tasks related to the support of sterile manufacturing, such as: supporting qualification and validation activities related to routine manufacturing and launch projects, review and approval of GMP relevant documentation, Change Control, Deviation handling and representation of QA Compliance Qualification & Validation in dedicated project(s).
Major accountabilities:
Represent QA Compliance Qualification
Erfahrung: Professional experience in Quality Control/Quality Assurance or in the manufacturing of pharmaceutical drug products and Steriles/Biotechnology
Profound knowledge of cGMPs
Technical/Professional Knowledge and Skills
Knowledge of the current pharmacopoeia requirements including technical methods (USP, Ph. Eur, JP,Coaches and inspires people to achieve team goals
Superior problem solving, decision making and planning skills as appropriate.
Sets clear priorities for task for him/herself and the team.
Excellent knowledge of GMP regulations
Ability to work under time pressure
Focus on customer satisfaction
Recognized expert; networking with CPL/QA/QC, PUs, TRD, HSE, RegCMC, SCM, etc.
Support PUs to guarantee high quality and current GMP
Provides new solutions for existing processes and is committed to continuous improvements
Assumes responsibility and sets clear priorities
Is a strong team player
Readily shares information and professional knowledge
Is a role model
Communicates on all levels within and outside own function
Works independently, efficiently and contentiously
Is committed to quality, GSU and GMP
Is goal-oriented and flexible
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) (see below) For further details feel free to call me
I am looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges