| Computer System Validation Consultant |
Contract
|
| Computer System Validation Consultant - 15 years experience of development and validation of global computer systems in large pharma companies.
In depth knowledge of computer system validation processes, system development lifecycle, 21CFR Part 11 assessment and validation project management as applied to regulated areas
A flexible, practical and proactive approach and an ability to adapt to changing priorities
Excellent communication skills (written and v...more |
| Location: East Anglia, UK |
Salary: £350 per day |
|
| Research Officer |
Permanent
|
| Research Officer - Pharmacology graduate with 16 years laboratory experience from novel drug screening to analysis of clinical samples. Also completed PhD (subject to viva). Wide range of laboratory techniques include ELISA, HPLC, GC, FACS, cell functional studies. Managing medical university laboratories; varied duties covering all aspects of clinical research and scientific support. Protocol and ethics writing, sample collection and analysis, statistics, presentation of results.
PC literate: ...more |
| Location: South Wales, will relocate to south West/South East UK. |
Salary: £21,000 + |
|
| It Director/Programme Manager |
Permanent
|
| It Director/Programme Manager - 15 years in IT management. Key Skills: Leadership, Business Strategy and Development, Implementation, Negotiation, Contract Management, Programme Planning, Budgeting, Project Monitoring and Control, BPR, Risk Management and Contingency Planning.
Current role includes:
• Senior management team member responsible for IM operational systems (ITIL) and IM project delivery in conformance with GxP quality standards.
• Liaison with global IM community, leveraging...more |
| Location: South West preferred, UK |
Salary: £60k |
|
| Quality Assurance, Regulatory Compliance, Validation |
Permanent
|
| Quality Assurance, Regulatory Compliance, Validation - A Senior Quality/Technical Manager with 12 years experience in Quality Assurance, Control, Systems Management and Validation in the Pharmaceutical sector
Major Achievements:
Registration transfer from ISO9002:1994 to ISO9001:2000
Developed an electronic CAPA and deviation system in conjunction with IT department
Validation of methodology and techniques as part of the site cleaning validation master plan
&#...more |
| Location: UK |
Salary: Negotiable |
|
| Senior Consultant |
Contract
|
| Senior Consultant - Senior data management and computer systems validation consultant - UK based. More than 18 years pharmaceutical and CRO experience designing, implementing and operating clinical IT systems (DM, CTMS, Pharmacovigulance, e-Clinical Systems). 21-CFR-Part 11 experience. Prospective and retrospective CSV projects, including audit and project management . Newbury, Berkshire...more |
| Location: Newbury, Berkshire, UK |
Salary: £300- £600/day |
|
| Project Manager |
Contract
|
| Project Manager - An experienced product and process Project Manager with formal training in the latest best practice techniques, including Risk Assessment and FMEA, and over 10 years hands-on using MS Project.
I can demonstrate a proven track record in delivering a diverse range of projects on time and within budget, from the introduction of new products, to the development and implementation of new high-speed, high volume manufacturing equipment.
My projects have included, high-speed and h...more |
| Location: South East, UK |
Salary: £32/hr |
|
| Regulatory Affairs |
Permanent
|
| Regulatory Affairs - Ten years Pharmaceuticl Industry.
Involved in Method, Process, and Transfer Validation along with Intermediate Precision.
INSTRUMENTATION: NMR, IR, UV, HPLC, ESR, GLC, AA, GC/MS, Karl-Fischer & Electrode Chemistry.
Have six months experience in Regulatory Affairs Executive-Chemist : Work within Chemical Manufacturing Control (CMC) group in Global Post Approval Registration (GPAR),except USA. Activities involve: updating/providing/preparing Part IIC. and Part IIF. Comm...more |
| Location: Beds, Berks, Bucks, Herts, Middx, Oxon and Surrey |
Salary: £30k |
|
| Business Analyst/Validation Consultant |
Permanent
|
| Business Analyst - Business Analyst / Computer Systems Validation Consultant – UK, willing to relocate. Accomplished professional with more than 5 years experience as a business consultant specialising in Business Process Analysis and Re-engineering, Excellent knowledge of CFR 21 Part 11 and GAMP4. Compliant package implementation within the Pharmaceutical Industry. More than 2 years experience as a Project Manager in the Pharmaceutical, Automotive, Electrical Industries. Managed implementation...more |
| Location: Europe/USA/Asia |
Salary: £50k |
|
| Validation Specialist |
Permanent
|
| Validation Specialist - Senior Validation Consultant –,
· Looking for An opportunity in PA/NJ/DE –Greater Philadelphia area
· 5 years experience in development, reviewing and executing validation documents, SOPs and protocol in cGMP facility. Experience in SDLC and VSR.
· Experience in the field of Process Control System Validation and Computer System Validation and compliance, 21 CFR Part 11 assessments and audits
· Experience with validation of Allen Bradley Contrologix PLC system Va...more |
| Location: Pennsylvania, New Jersey, Delaware |
Salary: $ 40 HOUR + Benefits |
|
| SAS Programmer |
Contract
|
| SAS Programmer - SAS Programmer - 17 months of SAS programming experience in the pharmaceutical industry as on March 2004. Good knowledge of SAS/BASE, SAS/STAT, SAS/GRAPH & MACRO in the UNIX environment. Good knowledge of Applied Statistics in the pharmaceutical and marketing domains. Good communication and presentation skills. Also have knowledge of Oracle, Perl and PL/SQL. Therapeutic areas worked include Neurology, Respiratory and Metabolism. Experienced in Phase 1 and 3 studies.
Skills in...more |
| Location: Bangalore - India |
Salary: £20-£30 pounds per hour |
|
|
