| QA Analyst |
Permanent
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| QA Analyst - Worked on projects from analytical validation exercises through to sample analysis.
Worked in a GMP/GLP environment
Qualified as an Internal Auditor ISO 9000 standard.
Qualified as a COSHH assessor.
Computer skills include use of All Microsoft offices packages.
Familiar with LIMS database systems
Verification of methods and production of SOP’s.
Good working knowledge of the following analytical techniques: HPLC, titration, moisture meter, FTIR, UV-VIS,
Knowledge of DNA syn...more |
| Location: north west |
Salary: > £21 k |
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| Senior Validation Consultant |
Permanent
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| Senior Validation Consultant - Senior validation consultant (pharmacist) with 15 years of experience in validation (laboratory systems, cleaning, computer systems, manufacturing equipment and utilities) and development (analytical methods (biological and chemical), product & process). Assessed and developed quality systems (e.g. preparation of ISO certification), performed 21 CFR Part 11 and regulatory compliance assessments and provided training services. Managed project teams. Fluent in Dutch ...more |
| Remediation Engineer |
Contract
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| Remediation Engineer - An experienced Analytical Chemist and Validation Consultant with around seven years of experience working within the pharmaceutical industry. Experienced in writing documentation associated with the validation of laboratory equipment including computer systems. Experience of current worldwide quality standards for computer system validation and 21 CFR Part 11.
Willing to relocate worldwide, and adapt very easily to new environments. A highly motivated and dedicated t...more |
| Location: Singapore |
Salary: £28 |
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| Assistant Quality Control Manager |
Permanent
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| Assistant Quality Control Manager - I am a Science graduate with further qualifications in Management and have some 19 years experience in the Veterinary Pharmaceutical industry. My current duties include Training, Equipment Validation, Out of Specification Investigation, Document checking, work scheduling, experience of raw material and final product testing. I am also the Laboratory Health and Safety representative. I write Standard Operating Procedures, and prepare DQ, IQ, OQ and PQ documents...more |
| Location: Tayside, Scotland |
Salary: £28000 to £36000 |
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| process chemist/ research chemist |
Permanent
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| process chemist/ research chemist
B.Sc ( Chemistry Hons), B.tech ( polymer Tech) & Ph.D in Chemical Engineering.I have 10 years experience in
pharmaceutical,chemicals and polymer industries.
I am therefore requesting you to consider me in this regards.
regards
any location in UK...more |
| Location: any location in UK |
Salary: Min £20000/-pa |
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| CSV/Automation Systems Validation Engineer |
Contract
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| CSV/Automation Systems Validation Engineer - Experienced automation engineer specialising in computer and automation systems for the pharmaceutical industries.
Qualified to Euro Engineer status, conversant with European and FDA cGMPs including 21cfr part 11, life cycle documentation and quality procedures.. ...more |
| Location: UK, Flexible |
Salary: Neg. |
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| Snr consultant or Consultancy Manager |
Permanent
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| Snr consultant or Consultancy Manager - Senior Consultant – UK, Accomplished professional with 2 years experience as a business consultant in the Pharmaceutical Industry. Specialising in drug safety and regulatory compliance (CFR21pt11, E2B). Managed Implementations of safety systems and registration monitoring systems within the Pharmaceutical Industry also managed validation projects within the drug safety area. More than 7 years experience as a Project Manager in the Pharmaceutical, Asset Man...more |
| Location: Southern UK |
Salary: £45000 - £50000K per Annum |
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| Computer Validation Specialist |
Contract
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| Computer Validation Specialist - An experienced Computer Systems Validation (CSV) Specialist (16 years Process Automation, last seven of those specialised in Computer Validation). Looking for challenging roles in the field of CSV implementation. I have a specific interest in process consulting (the design and application of CSV methodology for effective implementation).
Previous experience: pro and retrospective CSV. QC practices, PLC, DCS, Platform validation, 21CFR11, software developmen...more |
| Location: Europe |
Salary: TBD |
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| quality /regulatory in (bio)pharmaceutical sector |
Contract
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| quality /regulatory in (bio)pharmaceutical sector - Pharmacist PhD with more than 15 years experience in bio(pharmaceutical) operations (QA, QC, validation, development and regulatory affairs). Most recently as facility senior manager and Qualified Person. Managerial responsibility for departmental budgets, capital expenditure and human resources management of QA, QC, validation and regulatory personnel.
As QP, responsible for batch disposition of commercial and investigational products and fac...more |
| Location: Benelux/Europe |
Salary: negotiable |
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| Quality Assurance |
Contract
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| Quality Assurance - A highly innovative and competent analyst is seeking to move into a QA role with an eventual goal of gaining QP Status. With over 6 years of experience in analytical QC/R&D with major pharmaceutical & biotech companies covering all aspects of the drug development, market authorisation, manufacturing & testing plus instrument & process qualification/validation.
Knowledge & awareness of Quality Systems, MHRA/EMEA and FDA regulation UKAS/NAMAS, cGXP, ICH, ISO guidelines and pha...more |
| Location: NW England |
Salary: £18,000 |
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