Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
QA Coordination Expert
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Engineering, Support, Engineer
Projektbeschreibung
One of our clients, a multinational company in the pharmaceutical industry currently requires a QA Coordination Expert
Start: ASAP
End: 31/12/13
Location: South of Brussels
FUNCTION AREA
- Raises and maintains the status of quality in the organisation and enables a company to promote itself as one that provides quality goodsand services.
- Involves Total Quality Management (TQM) programmes and thedevelopment of standard procedures in accordance with the client's standards and cGMP Regulations.
- Raises and maintains the status of quality in the organisation and enables a company to promote itself as one that provides quality goodsand services.
- Involves Total Quality Management (TQM) programmes and the development of standard procedures in accordance with the client's standards and cGMP Regulations.
DISCIPLINE
Develops, assures and maintains the quality of the product and processes
- Standard procedures
- Quality audits/review
- Key Performance Indicators (KPIs)
- Process re-engineering
KEY ACCOUNTABILITIES
* Ensures quality oversight of all activities related to the area of responsibility
* Ensures batches of the intermediate product related to the area of responsibility are released in a timely manner
* Ensures deviations, complaints, change controls, OOS investigation, maintenance and calibration plans are reviewed and handled in a timely manner
* Ensures critical topics are adequately and timely escalated to higher management
* Represents QA in all operational meetings related to the area ofresponsibility (staff meetings, deviation, CAPA, RPC follow-upmeetings, )
* Supervises a team of technicians, distributes their work and isresponsible for their training and development plan
* Performs internal audits
* Contributes to local and/or transversal improvement projects toensure the compliance level is maintained in line with cGMP and theclient's standard requirements
* Provides QA support to new product introduction projects and related validation activities
* Understands technical/production problems and evaluates theirpotential impact on product quality. Escalates complex problems to N+1
* Compiles quality reviews
PREREQUISITES:
Education :
Scientific university degree (Pharmacist, Engineer or equivalent)
Knowledge :
Very good knowledge of English
* Knowledge of GMP regulated environment
Experience :
Minimum 2 years of experience in a Pharmaceutical/Bio/Medical deviceenvironment or equivalent
Tags: QA, Quality Assurance, Pharmaceutical, Pharmaceutique, KPI,Quality Management, GMP
Start: ASAP
End: 31/12/13
Location: South of Brussels
FUNCTION AREA
- Raises and maintains the status of quality in the organisation and enables a company to promote itself as one that provides quality goodsand services.
- Involves Total Quality Management (TQM) programmes and thedevelopment of standard procedures in accordance with the client's standards and cGMP Regulations.
- Raises and maintains the status of quality in the organisation and enables a company to promote itself as one that provides quality goodsand services.
- Involves Total Quality Management (TQM) programmes and the development of standard procedures in accordance with the client's standards and cGMP Regulations.
DISCIPLINE
Develops, assures and maintains the quality of the product and processes
- Standard procedures
- Quality audits/review
- Key Performance Indicators (KPIs)
- Process re-engineering
KEY ACCOUNTABILITIES
* Ensures quality oversight of all activities related to the area of responsibility
* Ensures batches of the intermediate product related to the area of responsibility are released in a timely manner
* Ensures deviations, complaints, change controls, OOS investigation, maintenance and calibration plans are reviewed and handled in a timely manner
* Ensures critical topics are adequately and timely escalated to higher management
* Represents QA in all operational meetings related to the area ofresponsibility (staff meetings, deviation, CAPA, RPC follow-upmeetings, )
* Supervises a team of technicians, distributes their work and isresponsible for their training and development plan
* Performs internal audits
* Contributes to local and/or transversal improvement projects toensure the compliance level is maintained in line with cGMP and theclient's standard requirements
* Provides QA support to new product introduction projects and related validation activities
* Understands technical/production problems and evaluates theirpotential impact on product quality. Escalates complex problems to N+1
* Compiles quality reviews
PREREQUISITES:
Education :
Scientific university degree (Pharmacist, Engineer or equivalent)
Knowledge :
Very good knowledge of English
* Knowledge of GMP regulated environment
Experience :
Minimum 2 years of experience in a Pharmaceutical/Bio/Medical deviceenvironment or equivalent
Tags: QA, Quality Assurance, Pharmaceutical, Pharmaceutique, KPI,Quality Management, GMP
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Ingenieurwesen/Technik, Sonstiges