| Chemical process engineer |
Contract
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| Chemical process engineer - Junior chemical process engineer- France, willing to relocate. I also have a master in chemistry.
I have an experience in laboratory research ( part of my master in chemistry studies) and another experience in production as a part of my engineering studies in an international pharmaceutical laboratory.
I am fluent in speaking French and English with a good working knowledge of a number of other languages (lebanese, spanish and german).. ...more |
| Location: France, willing to relocate |
Salary: Negotiable |
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| Validation Consultant |
Contract
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| Validation Consultant - 14 years experience in the Pharmaceutical industry,initially as a Company microbiologist and GMP Trainer and therafter in various contract Validation Engineer/Regulatory consultant roles .
Worked on several new facilities/refurb operations
and have managed both the documenation and execution sides from drafting of URS to Final summary reoports.
. UK/IRE...more |
| Location: UK/IRELAND |
Salary: £55/hour |
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| Computer Validation Engineer |
Permanent
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| Computer Validation Engineer - I have 6 years of recent Pharmaceutical industry experience as a Computer Validation Engineer. I have provided technical expertise on 21 CFR Part 11 and other cGMP related areas. I create and execute IQ/OQ/PQ protocols and help in writing SOPs and other related policy guidelines. Baltimore, MD...more |
| Location: Baltimore, MD, USA |
Salary: $75K |
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| Vaidation and Quality Assurance Consultant |
Contract
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| Vaidation and Quality Assurance Consultant - An experienced consultant with a solid background in quality management systems (ISO & cGMP); industrial processes and manufacturing techniques.
Experienced in life cycle validation techniques as described in GAMP. As well as quality management tools such as SPC, Pareto, Continuous improvement (Kaizen), FMEA, BPR, MPR/MPRII, JIT, Kanaban. Has worked continually and successfully in several process industries including Medical Devices; Active Pharmace...more |
| Location: Manchester, UK |
Salary: £40 GBP per hour |
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| Engineering Consultant Bio Process Automation, CSV, Instrumentation, QA |
Contract
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| Engineering Consultant Bio Process Automation, CSV, Instrumentation, QA - Senior Computer Systems Validation Consultant – Netherlands, willing to relocate.
Accomplished professional with more than 10 years industrial experience as a engineering consultant in the Pharmaceutical Industry specialising in Computer Compliance (CFR21pt210, 211 & pt11) both retro & prospective validation using GAMP4. Compliant package implementation within the Pharmaceutical Industry. More than 10 years of experience ...more |
| Location: The Netherlands |
Salary: negotiable |
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| Pharmaceutical QA/QC or manufacturing |
Permanent
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| Pharmaceutical QA/QC or manufacturing - Twenty-four (24) years’ industrial experience (Research & development, Plant Operations, Technical management and QC) gained in the Pharmaceutical and Specialist chemicals Industry. Comprehensive awareness of FDA and MHRA requirements, audits, impact on product development and commercialisation. Experience of lab & pilot plant process scale-up and commercial production. Technical skills:
Application of cGMP, HAZOP, ESH and COSHH
Good...more |
| Location: UK and Ireland |
Salary: £20,000-£35,000 |
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| Research Technician |
Permanent
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| research technician - An experienced Research Technician with a proven track record of success in Gene Regulation and Molecular Genetics. Strong analytical, project activities and database development experience. Results orientated and project focussed producing high levels of accurate data. Experience of developing and maintaining databases, data analysis, project development and delivery, working to regulation and teaching highly skilled scientists.
CURRENT CAREER ACHIEVEMENTS INCLUDE:
...more |
| Location: Northwest, UK |
Salary: £19,000 p/a |
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| Operations Director |
Contract
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| Operations Director - A quality driven interim operations executive, QP and site manager, having successfully improved key production facilities and operations in blue-chip multinational pharmaceutical companies.
Particular Strengths
Qualified Person for release to market of solid dose, sterile, liquid and topical products.
Change management, reorganisation and rationalisation of complex production and organisational dynamics to maximise utilisation of resources ...more |
| Location: UK |
Salary: £300 / day |
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| In Vivo Pharmacologist / Clinical Project Manager / Medical Writer |
Permanent
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| In Vivo Pharmacologist / Clinical Project Manager / Medical Writer - Eleven years experience testing drugs in animal models of heart failure, hypertension, thrombosis, restenosis, atherosclerosis, peripheral vascular disease, stroke, diabetes, ischemia-reperfusion injury, acute and chronic inflammation and cancer. I have also tested blood substitutes and drugs to increase and inhibit angiogenesis. I have worked in clinical research as a project manager, medical liaison and medical writer. I h...more |
| Location: Blue Springs Missouri, USA |
Salary: negotiable and flexible |
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| Director, Manager, QA, NJ. USA |
Permanent
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| director, manager, QA, - Teaching Animal Science/Biotechnology at a University or College level. Develop training programs for all levels of research staff in large corporations and universities. I possess superior presentation and management skills. 14.5 years of experience in a general management roles, including ten years of experience leading projects and GLP/quality assurance. I am highly skilled at structuring departments for maximum efficiency and effectiveness. expertise in negotiation...more |
| Location: New Jersey,USA |
Salary: $100,000 |
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