Search Results: 88 vacancies
...Secretarial or computer Certificate/Science Diploma or equivalent (preferable but not essential)
Documentation control experience ideally in a GMP/GLP environment would be an advantage
An equivalent combination of education and experience may be accepted as a satisfactory...
...Receipt and processing of test samples in LIMS.
Safe and compliant disposal of all laboratory generated waste.
Generation of GMP compliant SOPs, Protocols and reports.
Carry out data calculations and basic statistics.
Assist in internal, regulatory and client...
...within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
Generation of GMP compliant SOPs, Protocols and reports.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing....
...immunological methodologies to meet client requirements and/or company strategic objectives.
Draw up study plans / protocols ensuring full GMP regulatory compliance, where appropriate.
Execution of study plans and / or complex methods in the laboratory for transfer /...
£41.2k - £44.6k per annum
...perform and review laboratory investigations.
* Assist in the creation and maintenance of laboratory SOPs and validation documents for GMP lab test procedures and systems.
* Assist in the writing of functional area status reports, regulatory documents, and process...
£30k - £42.9k per annum
...required or equivalent science discipline.
* A good knowledge of aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines.
* Lab experience within industry - Bioburden / Endotoxin / Growth...
£50k - £60k per annum
...the company at client and regulatory meetings and audits.
* Ensure all activities in the department are performed in accordance with GMP, relevant SOP’s and policies.
* Participate in management activities within the operations group to ensure timely and appropriate availability...
£ 43 - 56 per hour
...Computer Technology.
* 5-10 years’ experience in process automation, with relevant experience of batch processing and DCS platforms in a GMP environment in the pharmaceutical industry.
* 3 years’ experience of the 21 CFR Part 11 requirements for automated systems in the...
...maintenance program is adequate and timely).
Development and implementation of appropriate supporting documentation, which complies with GMP in conjunction with the other team members.
Project planning, in detail, in support of major projects, product/process transfer etc....
...required or equivalent science discipline.
* A good knowledge of aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines.
* Lab experience within industry - Bioburden / Endotoxin / Growth...
Team Horizon
County Mayo
1 day ago
...Nurtures a risk-taking environment and encourages employees to reach for new milestones.
Ensures department adherence to regulatory and GMP requirements.
Promotes quality and customer satisfaction as a way of life in all department activities.
Intuitively identifies...
...lines in a time frame in all production areas.
Working nights and including Sunday as working week.
Adherence to procedures
~ GMP Daily hygiene and housekeeping
~ Good Housekeeping is essential.
~ Cleaning instruction cards ensure cleaning instruction cards...
...automation discipline, with a minimum of 10 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip or relevant GMP manufacturing environment. The ideal candidate will have excellent communication & problem solving skills as well as strong stakeholder...
...perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
Do you have expertise in working to GMP standards, within a Quality Assurance function?
Are you a motivated people leader, with the desire to play a key role in career...
...environmental, health, and safety goals by adhering to all general site and department safety policies.
Essential Behaviours:
Adhering to GMP cleanroom behavioural procedures at all times.
Completing all GMP paperwork RFT, in a timely manner and as per GDP, allowing for...
...Operating Procedures.
Qualifications
Third level education in a relevant Science / Engineering course or 2 year's experience in GMP manufacturing is essential
Desired: Three years plus of Knowledge of cGMP and regulatory requirements relating to the pharma/...
...continuous improvement within the department, encouraging risk-taking and innovation.
Ensure departmental adherence to regulatory and GMP requirements, promoting quality and customer satisfaction in all activities.
Proactively identify and mitigate technical risks,...
...Requirements:
~ A third level qualification in an appropriate discipline is desirable.
~4-5 years’ Experience within a regulated GMP environment is desirable
~1 year plus experience in the day-to-day operation of the quality system in a highly regulated combination...
...Your Key Activities will include, but are not limited to:
~ Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
~ Perform activities associated with the compounding, filling and capping of an aseptic process.
~ Prepare components...
...device industry, including;
Competent working knowledge of recognized Quality Management Systems (e.g. ISO9001/ ISO13485/ ISO14971/ GMP),
Awareness of relevant laws and regulations (e.g. CE/ FDA/ PAL)
Competency in conducting technical review of all documentation/ communications...
