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Validation Coordinator - Filling
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Engineering
Projektbeschreibung
One of our clients, an international company in the pharmaceutical industry currently requires a Validation Coordinator to coordinate PQ validation activities
Start: ASAP
Length: min. until 1/6/2015
Location: South of Brussels
KEY RESPONSIBILITIES:
* In collaboration with User, technical services and QA, fixe validation strategy
* Writte PQ Protocol and Report; Risk assessment and Gap Analyis
* Coordinate validation activities
* Coordinate Deviation links to validation activities
* Presentation of the validations during audits/inspections.
* Communicate regularly validation status
* Possible collaboration on specific projects on continuous improvements (transversal CAPA).
PREREQUISITES:
Education
* Engineering degree (pharma, processes, chemistry, biotechnology)
Knowledge:
* Good knowledge of written and spoken French and English
* Good communication skills
* Ability to work under heavy pressure due to the requested flexibility and reactivity of the activities
* Autonomous and achievements oriented
* Hands-on mentality
* Ability to work in project teams in a multidisciplinary environmentand a matricial organization
* Familiar with validation cleaning, sterilisation, Environmental monitoring, media simulation, clean utilities, filling machine
Experience:
* Minimum 5 years' experience in the pharmaceutical industry
* Previous experience in Validation PQ
* Previous experience in a GMP environment
* Asset: experience in Filling or Formulation area
Tags: validation, pharmaceutical, GMP, filling, clean utilities, cleaning, environmental monitoring, PQ, risk assessment, pharmaceutique, CIP, SIP
Start: ASAP
Length: min. until 1/6/2015
Location: South of Brussels
KEY RESPONSIBILITIES:
* In collaboration with User, technical services and QA, fixe validation strategy
* Writte PQ Protocol and Report; Risk assessment and Gap Analyis
* Coordinate validation activities
* Coordinate Deviation links to validation activities
* Presentation of the validations during audits/inspections.
* Communicate regularly validation status
* Possible collaboration on specific projects on continuous improvements (transversal CAPA).
PREREQUISITES:
Education
* Engineering degree (pharma, processes, chemistry, biotechnology)
Knowledge:
* Good knowledge of written and spoken French and English
* Good communication skills
* Ability to work under heavy pressure due to the requested flexibility and reactivity of the activities
* Autonomous and achievements oriented
* Hands-on mentality
* Ability to work in project teams in a multidisciplinary environmentand a matricial organization
* Familiar with validation cleaning, sterilisation, Environmental monitoring, media simulation, clean utilities, filling machine
Experience:
* Minimum 5 years' experience in the pharmaceutical industry
* Previous experience in Validation PQ
* Previous experience in a GMP environment
* Asset: experience in Filling or Formulation area
Tags: validation, pharmaceutical, GMP, filling, clean utilities, cleaning, environmental monitoring, PQ, risk assessment, pharmaceutique, CIP, SIP
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Ingenieurwesen/Technik