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Manufacturer

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GMP Inspector

Cullen - Full
GMP Inspector Reporting to a GMP Inspection Manager, the GMP Inspector will be responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The Manufacturing Compliance Specialist will evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation European Community Directives, Regulations and Guidance. These sites may include; • Manufacturers and distributors of medicinal products. • Manufacturers of investigational medicinal products. • Sites involved in the storage of medicinal products. •...
22-10-2018 - lifescience.ie save
 

Interim Logistics Manager (12-18 Mths) - Dublin

Dublin - Interim - Full time
Leading international FMCG manufacturer and distributor now seek to hire an Interim Logistics Manager (12-18 Months) to undertake a cost reduction and network efficiencies project within the Irish manufacturing and distribution sites. Working from their South Dublin facility and reporting to the Director of Logistics, you will review inventory, warehousing and distribution operations to identify cost reduction and network efficiencies along with developing and implementing the plans required to achieve these objectives. Minimum Requirements: Extensive logistics experience within an FMCG...
14-08-2017 - jobsearch.ie save
 

Senior GMP Inspector

Cullen - Full
Senior GMP Inspector Our client, a large regulatory body, are currently recruiting for a Senior GMP Inspector to join their team. As Senior GMP Inspector, you will carry out GMP inspections and scientific evaluation across the full range of manufacturing and testing sites in accordance with the requirements of GMP. Responsibilities • Carry out GMP inspections and scientific evaluation across the full range of sites in accordance with the requirements of EU GMP • Supporting the GMP Manager in the management and ongoing development of the GMP inspection team • Providing leadership, support and...
04-07-2018 - lifescience.ie save
 

Senior Planner

Part
An exciting opportunity for a Senior Planner to join Ireland's leading independent manufacturer of concrete construction materials. You will be part of the Planning and Environmental Team based in Co Meath Key Responsibilities & Accountabilities: The Planning and Environmental Department is a small group of professionals working with the Board of Directors to expand the resource base of the company through identification of new mineral prospects and securing regulatory consent. The position of Senior Planner is responsible for:- Planning Applications Planning Compliance submissions Managing...
07-08-2017 - jobsearch.ie save
 

Account Manager Chromatography

Cross
Our client is a leading manufacturer and supplier of OEM laboratory equipment and instrumentation. They are seeking an Account Manager Role is anywhere in Ireland. Responsibilities Ensure delivery of targets by selling Chromatography instruments, HPLC, Gas Chromatography, Ion Chromatography and Software to both the private and public sectors within the defined geographical area of the 32 counties. The position holder will need to interface with all members of sales, support and service groups within Chromatograph. In addition, support cross-selling activities with other CMD sales & Thermo...
15-05-2018 - lifescience.ie save
 

Product Design & Development Manager

Mayo - Experienced - Full
Product Design & Development Manager My client, a leading European manufacturer & supplier of safety products are looking for experienced Product Design Managers to join their team. The Role Required to bring innovative products from concept & design to the market, liaising with departments internally to deliver. Previous experience with PPE would be essential. Co Mayo. Responsible for the full product 'life cycle' including design and development, sourcing materials, testing, certification, packaging, marketing and commercialisation of the product from concept to market. Manage the delivery...
06-08-2017 - jobsearch.ie save
 

Qualified Person QP

Dublin - Permanent - Experienced
Qualified Person QP Our Dublin based client are currently recruiting for a Qualified Person to join their team. This is a permanent opportunity and the ideal candidate will have OSD experience, however other experience will be considered. Experience releasing batches is a must and as QP you will also be responsible for supporting Quality Systems and ensuring GMP compliance across the site. Responsibilities • Responsible for the disposition and release of product manufactured and/or packaged on site or by 3rd Party Manufacturers & New Product Introduction Products • Ensure that each batch...
23-04-2018 - lifescience.ie save
 

API Third Party Manufacturing Manager

Dublin - Permanent
API Third Party Manufacturing Manager Our client, a global pharmaceutical organisation are currently recruiting for an API Third Party Manufacturing Manager. As API Third Party Manufacturing Manager you will be the primary point of contact for technical oversight and support of third party manufacturers producing API, intermediates, and starting materials for the organisation. This is a permanent opportunity based in Dublin. Responsibilities • Manage the technical support (product and process expertise) of API manufacturing processes executed at the third party manufacturers. This includes a...
27-02-2018 - lifescience.ie save
 

Inspections Scientific Officer

Dublin
Inspections Scientific Officer Our Dublin based client are currently recruiting for an Inspections Scientific Officer to join their team. The successful candidate will provide technical and organisational support to the teams responsible for licensing, registration and the inspection of manufacturers of human medical products, notified bodies for medical devices and other areas across the organisation. Responsibilities • Liaise with the Licensing and Planning sections in relation to applications for authorisation of sites • Assess new applications and variations received for manufacturer’s...
21-01-2018 - lifescience.ie save
 

Administration Support

Dublin - Permanent
Administration Support Our client, one of the largest multinational companies based in Dublin is recruiting for Administration Support . You will join the team as the Administrative Support in Regulatory and Quality capacity. The Role is with a pharmaceutical giant in North Dublin and it is a permanent role. The Position • Administrative support in regulatory/quality capacity – proof reading, sending back defect units to manufacturer • Answering phone/other front of house duties such as post etc • Support for sales – VEEVA • Support for commercial • Assist with meetings • Customer support •...
31-12-2017 - lifescience.ie save
 

GMP Inspector

Cullen - Full
GMP Inspector Reporting to a GMP Inspection Manager, the GMP Inspector will be responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The Manufacturing Compliance Specialist will evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation European Community Directives, Regulations and Guidance. These sites may include; • Manufacturers and distributors of medicinal products. • Manufacturers of investigational medicinal products. • Sites involved in the storage of medicinal products. •...
18-12-2017 - lifescience.ie save
 

Sampling and Analysis Scientific Officer

Dublin - Full
Sampling and Analysis Scientific Officer Our Dublin based client is currently recruiting for Scientific Officer to the join their Market Compliance team. The successful candidate will assist the Market Compliance Manager in the day to day operation of the Sampling & Analysis programme. Responsibilities • Collection of samples from the supply chain, making arrangements for the analysis the samples • Review test results from the laboratories, and assist in the actioning of those test results • Perform examinations on the packaging and labelling of medicinal products from a compliance perspective...
28-11-2017 - lifescience.ie save
 

Regulatory Affairs Specialist

Cross - Permanent - Part
Regulatory Affairs Specialist Our client, a global medical device organisation requires a Regulatory Affairs Specialist to join their Regulatory Affairs Team on a permanent basis. The Regulatory Affairs Specialist will report directly into the Regulatory Affairs Manager. Responsibilities • Maintain an excellent understanding of global medical device regulations for specific jurisdictions as assigned such as regulatory requirements in accordance with ISO13485, MDD 93/42/EEC and FDA QSP 21CFR Part 820 as required • Ensure a thorough understanding of the products they are assigned • Communicates...
12-11-2017 - lifescience.ie save
 

Qualified Person QP

Cullen - Permanent - Experienced
Qualified Person Our client, a global pharmaceutical organisation are currently recruiting for a QP to join their team on a permanent basis. Responsibilities • Responsible for the disposition and release of product which are manufactured and/or packaged by the organisation or manufactured and/or Packaged by 3rd Party Manufacturers/Assemblers and New Product Introduction Products • Ensure that each batch released has been produced and tested in accordance with the current EU/FDA GMP Directives and the relevant marketing authorization o Ensure that the Marketing Authorisation and Manufacturing...
18-10-2017 - lifescience.ie save
 

RandD Production Team Leader (Generics)

Screen - Part
Our client is an Irish incorporated generic pharmaceutical company who are part of a wider group, a Belgian group of pharmaceutical companies with focus on the development and manufacturing of pharmaceutical products. They use 3rd Party manufacturers all over the world, all holding valid EU GMP and/or FDA approval. They license out their products to clients all over the world. The team behind the organisation has significant experience within the European generic industry and today these people are focused on bringing this know-how to Ireland & the US. As our client is a young company, their...
25-09-2017 - lifescience.ie save
 

Procurement Manager

Dublin
Procurement Manager Pharmaceutical Dublin Competitive Salary Due to an internal promotion a Procurement Manager is urgently required to join a leading global manufacturer based in Dublin. This is a unique opportunity to join a growing organisation that is focused on the design and production of high-tech and high quality products. Reporting into the Senior Operations Director you will be responsible for all procurement activity in Dublin. This is a real opportunity for a Procurement Manager to implement procurement strategy, policy and procedures across all areas of spend. Liaising with the...
17-09-2017 - lifescience.ie save
 

Chemistry and Life Science Account Manager

Cullen - Permanent
Chemistry and Life Science Account Manager Our Client is a leading manufacturer and distributor of specialised laboratory equipment for the Chemistry and Life Science research sectors and they are currently recruiting for a Chemistry and Life Science Account Manager to join their business on a permanent basis. This role will cover all 32 counties. Responsibilities • Identification and development of sales opportunities within the territories • Achieve quarterly and annual sales targets • Frequent demonstrations of our large range of laboratory equipment • Presentations and seminars within the...
10-09-2017 - lifescience.ie save
 

Development Leader

Part
Development Leader Our client a multinational medical device manufacturer is currently seeking a development leader to join their team. Reporting to WW Engineering Manager the role is responsible for the transfer from R&D and introduction of new lines onto the site. The purpose of this position is to co-ordinate the site development function to ensure new products and process are introduced in an efficient and effective manner, utilising leading technologies and methods. Role/Responsibilities: Develop, design, and evaluate processes and/ or equipment requiring novel and innovative approaches...
09-09-2017 - lifescience.ie save
 

Senior Regulatory Affairs Specialist

Part
Senior Regulatory Affairs Specialist Job purpose: The Sr. Regulatory Affairs Specialist will develop strategies for complex projects and issues related to regulatory processes, compliance activities, documents, submissions, investigations, product development planning and regulatory agency interaction. The Sr. Regulatory position will assist in mentoring and development of staff members as part of the role. Key responsibilities: • Key responsibilities will include (but are not limited to) the following: • Support global regulatory projects, including, but not limited to, the following areas: •...
01-09-2017 - lifescience.ie save
 

Projects Leader

Cross
Projects Leader Our client a multinational medical device manufacturer is currently seeking a Project Leader to join their team. Reporting to WW Engineering Manager the Projects Leader is responsible for leading a team to ensure the effective management of all project engineering activity on site. This role holds responsibility in ensuring the effective co-ordination of the site major capital projects in parallel with ongoing operations. Role/Responsibilities: Management of the site-wide project portfolio using the PPM process. Escalation of risks and issues arising that threaten project...
31-08-2017 - lifescience.ie save
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