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Process Improvement Consultant
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Consultant, Client
Projektbeschreibung
One of our clients, a multinational company in the pharmaceutical industry currently requires a Process Improvement Consultant
Start: 2/1/2014
Length: Minimum 6 months
Location: South of Brussels
FUNCTION DESCRIPTION
Our client is focusing on its Quality Improvement Plan (QIP). For this purpose, a cell project was created to concentrate on secondary process robustness.
For this part of the key plan, they are looking for 1 effective complementary worker that will focus on filling activities.
Their mission in collaboration with the product-process team will be toparticipate, improve and share robustness processes.
KEY RESPONSIBILITIES
* Follow the action plan of QIP
* Write, edite and trail:
- request for process change (RPC)
- Performance qualification (PQ)
- Standard operation procedure (SOP)
- check list
* Map process parameters
* Risk analysis: failure mode and effects analysis (FMEA)
PREREQUISITES
- Education : Master or Bachelor with experience with processes in pharma, chemistry or biotechnology
- Specific skills : effective, tight, pragmatical,outgoing and communicative
- Knowledge:
* Computing skills
-bases - Microsoft : Word, Excel, Outlook
-specific tools - group management portal (GMP)
- Experience:
* History with pharma environment
* Protocol writing
Tags: Process, Robustness, Pharmaceutical, Pharmaceutique, GMP, Risk analysis, Quality Improvement, Process Improvement
One of our clients, a multinational company in the pharmaceutical industry currently requires a Process Improvement Consultant
Start: 2/1/2014
Length: Minimum 6 months
Location: South of Brussels
FUNCTION DESCRIPTION
Our client is focusing on its Quality Improvement Plan (QIP). For thispurpose, a cell project was created to concentrate on secondary processrobustness.
For this part of the key plan, they are looking for 1 effective complementary worker that will focus on filling activities.
Their mission in collaboration with the product-process team will be to participate, improve and share robustness processes.
KEY RESPONSIBILITIES
* Follow the action plan of QIP
* Write, edite and trail:
- request for process change (RPC)
- Performance qualification (PQ)
- Standard operation procedure (SOP)
- check list
* Map process parameters
* Risk analysis: failure mode and effects analysis (FMEA)
PREREQUISITES
- Education : Master or Bachelor with experience with processes inpharma, chemistry or biotechnology
- Specific skills : effective, tight, pragmatical,outgoing and communicative
- Knowledge:
* Computing skills
-bases - Microsoft : Word, Excel, Outlook
-specific tools - group management portal (GMP)
- Experience:
* History with pharma environment
* Protocol writing
Tags: Process, Robustness, Pharmaceutical, Pharmaceutique, GMP, Riskanalysis, Quality Improvement, Process Improvement
Start: 2/1/2014
Length: Minimum 6 months
Location: South of Brussels
FUNCTION DESCRIPTION
Our client is focusing on its Quality Improvement Plan (QIP). For this purpose, a cell project was created to concentrate on secondary process robustness.
For this part of the key plan, they are looking for 1 effective complementary worker that will focus on filling activities.
Their mission in collaboration with the product-process team will be toparticipate, improve and share robustness processes.
KEY RESPONSIBILITIES
* Follow the action plan of QIP
* Write, edite and trail:
- request for process change (RPC)
- Performance qualification (PQ)
- Standard operation procedure (SOP)
- check list
* Map process parameters
* Risk analysis: failure mode and effects analysis (FMEA)
PREREQUISITES
- Education : Master or Bachelor with experience with processes in pharma, chemistry or biotechnology
- Specific skills : effective, tight, pragmatical,outgoing and communicative
- Knowledge:
* Computing skills
-bases - Microsoft : Word, Excel, Outlook
-specific tools - group management portal (GMP)
- Experience:
* History with pharma environment
* Protocol writing
Tags: Process, Robustness, Pharmaceutical, Pharmaceutique, GMP, Risk analysis, Quality Improvement, Process Improvement
One of our clients, a multinational company in the pharmaceutical industry currently requires a Process Improvement Consultant
Start: 2/1/2014
Length: Minimum 6 months
Location: South of Brussels
FUNCTION DESCRIPTION
Our client is focusing on its Quality Improvement Plan (QIP). For thispurpose, a cell project was created to concentrate on secondary processrobustness.
For this part of the key plan, they are looking for 1 effective complementary worker that will focus on filling activities.
Their mission in collaboration with the product-process team will be to participate, improve and share robustness processes.
KEY RESPONSIBILITIES
* Follow the action plan of QIP
* Write, edite and trail:
- request for process change (RPC)
- Performance qualification (PQ)
- Standard operation procedure (SOP)
- check list
* Map process parameters
* Risk analysis: failure mode and effects analysis (FMEA)
PREREQUISITES
- Education : Master or Bachelor with experience with processes inpharma, chemistry or biotechnology
- Specific skills : effective, tight, pragmatical,outgoing and communicative
- Knowledge:
* Computing skills
-bases - Microsoft : Word, Excel, Outlook
-specific tools - group management portal (GMP)
- Experience:
* History with pharma environment
* Protocol writing
Tags: Process, Robustness, Pharmaceutical, Pharmaceutique, GMP, Riskanalysis, Quality Improvement, Process Improvement
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Organisation/Management