| SYSTEMS / COMPLIANCE CONSULTANT |
Contract
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| SYSTEMS / COMPLIANCE CONSULTANT - Senior Computer Systems Compliance / Validation Consultant.
Member Institute of Electrical and Electronic Engineers 40280687
Professional Member Association for Computing Machinery 3815974
Professional Member Institute of Validation Technology 1000244
Member of British Computer Society 09530561
Member International Society for Pharmaceutical Engineering 223303
Professional with more than 10 years experience as a consultant in the Pharmaceutical Industry sp...more |
| Location: |
Salary: Negotiable |
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| validation |
Permanent
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| validation - Have over 6 yrs experience in the pharmaceutical industry, roles randing from Quality assurance to Process and computer validation.. houston Texas usa...more |
| Location: houston Texas usa |
Salary: $80,000 |
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| Research Scientist, QA Person, Regulatory Affairs and Microbiologist |
Permanent
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| Research Scientist, QA Person, Regulatory Affairs and Microbiologist - I am a positive and ambitious person. To date I have gained very good work experience in the Pharmaceutical Industry in Quality Assurance and in the Food Sector in both Quality Control and Product Development. With my Scientific based education and knowledge behind me, I would like to further my career in the Pharmaceutical/Science Sector.
. Liverpool (Merseyside) North West...more |
| Location: Liverpool (Merseyside) North West, UK |
Salary: £20000 - £30000 |
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| Validation Manager |
Permanent
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| Validation Manager - Validation or Quality Management with greater than 10 years in Pharmaceutical / Biotechnology industries: Experience inall aspects of validation Equipment, Process, Cleaning, Test Method, primary and secondary. Also experienced Project manager in support of Technology transfer, Refurbishment ,Process Re-engineering and Capital equipment purchases,
Knowledge of Quality Systems, Failure investigations, risk Management , Total Quality Management in combination with Business...more |
| Location: UK, Will relocate |
Salary: Negotiable |
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| Director |
Permanent
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| Director - Young Managing Director of Consulting Engineers Group
Candidate has MBA and Chartered Engineer/Chartered Scientist accreditation.
He has a proven reputation in the management of high technology and scientific businesses. He has successfully derived value from provision of capital projects and business services to clients operating in sectors including Research, Pharmaceuticals, Construction, Architecture and Business Consultancy.
He has an engaging manner and an acute busin...more |
| Location: North West, UK |
Salary: Negotiable |
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| Technical Author |
Contract
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| Technical Author - A Senior Technical Author, with a wide range of experience in the field of requirements elicitation, currently working in an IT environment for a pharmaceutical company producing high quality validation GSOP documentation to tight deadlines and fixed price budgets.
Central to my earlier role was the evolution of high-quality customer-facing services, where challenging measures of customer satisfaction were important benchmarks.
As a Regional Operations Manager I was res...more |
| Location: Kent, UK |
Salary: +£25/hr |
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| Validation, Compliance Consultant |
Contract
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| Validation, Compliance Consultant - Validation consultant, specialising in lab systems, quality systems and 21 CFR Part 11 work. Retrospective and prospective validation using GAMP 4.
10 years of pharma experience, including development work, QA, technology transfer, quality audits, GAMP 5 systems, 21 CFR Part 11 remediation plans, control systems for autoclaves, freeze dryers, and ovens.
. Hertfordshire...more |
| Location: Hertfordshire |
Salary: neg |
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| validation and regulatory compliance |
Contract
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| validation and regulatory compliance - QA
Validation
Compliance
Technical writing
GLP/GMP
Regulatory
Technical Support
Customer Complaints
Non Conformances
Technical Changes
Documentation
. worldwide...more |
| Location: worldwide |
Salary: £25-30/hr |
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| Project Management, Quality Management |
Contract
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| Project Management, Quality Management. Fourteen (14) years of experience in the information technology industry and more than nine years (9) of experience managing successful GMP, GLP, validation, and Title 21 CFR Part 11 software implementation, remediation, and assessment projects for FDA regulated industries.
A skill summary......
Pharmaceutical manufacturing industry 9 years
Medical Device manufacturing industry 3 years
Title 21 CFR Parts 210, 211 (cGMP) 9 years
Title 2...more |
| Location: United States |
Salary: 70-80 euro/hour |
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| Computer Validation |
Permanent
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| Computer Validation -
EDUCATION:
B.S. in Information System at Virginia Commonwealth University 2000
B.S. in Biology and Minor in Chemistry at OLD Dominion University 1996
TRAINING/CERTIFICATES:
• Oracle Database Administrator 1 and 2
• Data Warehousing
• GLP (Good Lap Practice)
• cGMP (Good Manufacturing Practice)
• ISO9001 (International Organization of Standardization)
• 21CFR Part 11
•
SECURITY CLEAREANCE
Secret DSS (DISCO)
SUMARY:
• Performed Performance testi...more |
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