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Quality Assurance Project Officer

Cullen - Permanent
Quality Assurance Project Officer Our client, a multinational pharmaceutical organisation are currently recruiting for a Quality Assurance Project Officer to join their Quality team on a permanent basis. Responsibilities • Development and maintain project plans • Track and report on site periodic ad-hoc projects • Provide support and assist team members on projects as required • Author and review Technical Agreements in accordance with procedure Review and maintain TA alignment within the organisations sites • Co-ordinate weekly reports/periodic metrics and or status updates from all relevant...
14-07-2017 - lifescience.ie save
 

Development Editor

Dublin
Excellent role with an established leader in Primary and Post Primary Education. This is your chance to bring your passion for primary education to publications (print and digital content) while working with a great company who encourage creativity and growth. You will be working with authors, commissioning editors and digital design teams to ensure that high quality content is produced and published for primary schools. You will be the point of contact for questions that arise during development, product and post launch of the contect. If you have a background in primary education and an...
07-08-2016 - jobsearch.ie save
 

Quality Specialist for growing Pharma company!

Dublin - Permanent - Part
Exciting new opportunity for Quality Specialist for a growing pharmaceutical company! Job Responsibilities: Partners with the Regulatory Affairs, Supply Chain and Pharmacovigilance to assist and participate in the assurance of compliance activities required to ensure that products supplied , are in accordance with cGMP their associated Marketing Authorisation, company standards and values. The incumbent is accountable for the following functions within their respective manufacturing cell: • Completion of Deviations and Change Control in partnership with the other departments. • Monitoring...
19-11-2015 - jobs.ie save
 

Senior Regulatory Officer

Cullen - Permanent
Senior Regulatory Officer Our client, a global healthcare organisation, requires a Senior Regulatory Officer to join their team on a permanent basis. This is an excellent opportunity to work within the growing biologics space in Ireland. Responsibilities • Execute operational labelling activities required for all generic and brand products for multiple product types • Ensure appropriate key goals are met on time, and maintain Compliance of regulatory based labelling: Summary of Product characteristics, Package leaflet and Prescribing Information • Maintain current knowledge of labelling...
03-05-2017 - lifescience.ie save
 

MES Recipe Author

Cork
An MES Recipe Author is required by a leading Global Pharmaceutical company based in Cork. The Cork campus has produced small molecule API for over 30 years and has built a new Biotechnology facility which will deliver the next generation of products to the global market. For over three decades the site has succeeded in fostering a working environment where team members take pride in both the excellence of their personal and collective contributions and the positive benefits they provide to patients around the world. This is an opportunity to work for a household name and to grow your career....
12-06-2016 - jobsearch.ie save
 

Procurement Manager (Indirect Goods & Services)

Limerick - Permanent - Part
Summary: The successful candidate will be responsible for managing and leading site-based sourcing strategies, activities and transactions for all indirect goods and services including (Capital Equipment, MRO, Capital Services, Lab Services & Supplies and all other facility goods and services). Essential Duties and Responsibilities include, but are not limited to, the following: * Responsible for end to end management of assigned categories, including the category strategy development, category sourcing plan execution, and projects to optimize value. * Strive towards continuous supplier...
12-11-2015 - jobs.ie save
 

QA Specialist

Our client is a leading global biotechnology company. They have best-in-class products in a number of therapeutic areas. They are seeking a QA Specialist for a global role with diverse responsibilities and a clear career path. Experience in Biologics is a big advantage. The position will require approximately up to 20% travel. RESPONSIBILITIES Reviewing batch documentation, data, certificates of analyses, and providing support to the QP function Supporting schedule adherence of material disposition Designing and implementing quality systems relating to batch disposition Maintaining and...
08-09-2016 - lifescience.ie save
 

Regulatory Affairs Manager

Dublin
Regulatory Affairs Manager is required for a South Dublin based Biopharmaceutical company that specialises in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. In July 2015 the site opened a $300million investment, which added significantly to the sites laboratory, filling, packaging and distribution (including cold chain) capabilities. The site is a fast paced, collaborative, team based working environment, where you get an opportunity to work with other highly skilled staff in a strategically important site in the companies global supply chain. This role...
26-02-2016 - jobsearch.ie save
 

Procurement Manager (Indirect Goods & Services)

Limerick - Permanent - Part
Summary: The successful candidate will be responsible for managing and leading site-based sourcing strategies, activities and transactions for all indirect goods and services including (Capital Equipment, MRO, Capital Services, Lab Services & Supplies and all other facility goods and services). Essential Duties and Responsibilities include, but are not limited to, the following: * Responsible for end to end management of assigned categories, including the category strategy development, category sourcing plan execution, and projects to optimize value. * Strive towards continuous supplier...
28-10-2015 - jobs.ie save
 

Process Scientist Biotech

Dublin
Our client is a major biotech based in west Dublin. For their growing team, they require a Process Scientist with experience in either upstream or downstream biotech processing. Responsibilities • Provide process science and technology expertise to support facility, equipment and disposables design. • Capture all aspects of the existing process at the donor site to ensure a Zero Defect Transfer is attained. • Capture knowledge through review of documentation, observation of batches, compiling process descriptions and flow diagrams, interacting and training with donating site personnel. •...
25-01-2016 - lifescience.ie save
 

Global Operations Pharmacovigilance (PV) Auditor

Dublin - Permanent - Full-time
Duties and Responsibilities Prepare and conduct internal and external audits Perform independent research of required topics and FDA, EMEA, TGA, Health Canada, WHO, PIC/S, MHLW, and other national, international, or supranational regulations (GxP and ICH) including assessment of applicability and impact on systems being audited. Provide independent review, comprehension, and discussion of departmental and corporate policies and procedures with multiple levels of employees and Management. Provide interpretation of complex regulations through research of current corporate and governmental...
31-01-2016 - jobsearch.ie save
 

Procurement Manager (Indirect Goods & Services)

Limerick - Permanent - Part
Summary: The successful candidate will be responsible for managing and leading site-based sourcing strategies, activities and transactions for all indirect goods and services including (Capital Equipment, MRO, Capital Services, Lab Services & Supplies and all other facility goods and services). Essential Duties and Responsibilities include, but are not limited to, the following: * Responsible for end to end management of assigned categories, including the category strategy development, category sourcing plan execution, and projects to optimize value. * Strive towards continuous supplier...
22-10-2015 - jobs.ie save
 

External Manufacturing Scientist (Drug Product)

Dublin
Our client is a Global Speciality Biopharmaceutical Organisation with based in Dublin. They are currently seeking a Principal Scientist with a strong PhD Chemistry background. This is an exciting, frontline, technical role in a rapidly growing pharmaceutical company. They outsource all of their manufacturing activities. Role/Responsibilities: This key role will support new product and technology introductions within the Global Supply Chain Organization of Technical Operations. Sterile product experience is essential as the main products being supported include sterile suspensions, solutions...
23-01-2016 - lifescience.ie save
 

Global Operations Pharmacovigilance (PV) Auditor

Dublin - Permanent - Full-time
Duties and Responsibilities Prepare and conduct internal and external audits Perform independent research of required topics and FDA, EMEA, TGA, Health Canada, WHO, PIC/S, MHLW, and other national, international, or supranational regulations (GxP and ICH) including assessment of applicability and impact on systems being audited. Provide independent review, comprehension, and discussion of departmental and corporate policies and procedures with multiple levels of employees and Management. Provide interpretation of complex regulations through research of current corporate and governmental...
24-01-2016 - jobsearch.ie save
 

Regulatory Affairs Submissions Professionals

Dublin - Permanent
Regulatory Affairs Submissions Professional Our Client, a Pharmaceutical Manufacturing company based in Dublin is recruiting for a Regulatory Affairs Submissions Professional to their RA team on a permanent basis. The Regulatory Submissions Professional will report directly into the Regulatory Affairs Manager. Responsibilities • Prepare the Regulatory Submissions Pipeline • Verify and send project request to the sourcing partner • Review proposals from the sourcing partner in relation to submission plan/approach and provide input and information about priority and start-up date • Estimate...
01-11-2015 - lifescience.ie save
 

Global Quality Auditor - Dublin North

Dublin - Permanent - Experienced - Full time
Global Pharmaceutical Company based in North Dublin is looking for experienced Global Quality Auditors to join their team. Duties and Responsibilities: Provide objective audits of internal GXP systems and external businesses Management in order to accurately depict the status of compliance and to foster improvements based on current GXP references and interpretations. Prepare and conduct internal and external audits globally Perform independent research of required topics and FDA, EMEA, TGA, Health Canada, WHO, PIC/S, MHLW, and other national, international, or supranational regulations (GxP...
31-12-2015 - jobsearch.ie save
 

Global Quality Auditor

Cullen
Global Quality Auditor Our client, a global mulitnational pharmaceutial and generics company require a Global Quality Auditor to join their team. The Global Quality Auditor will provide objective audits of internal GXP systems and external businesses in order to accurately depict the status of compliance and to foster improvements based on current GXP references and interpretations. Responsibilities • Prepare and conduct internal and external audits • Provide independent review, comprehension, and discussion of departmental and corporate policies and procedures with multiple levels of...
28-10-2015 - lifescience.ie save
 

Process Cleaning Representative

Cork - Parts
Process Cleaning Representative is required by a leading Global Pharmaceutical company based in Cork. The Cork campus has produced small molecule API for over 30 years and has built a new Biotechnology facility which will deliver the next generation of products to the global market. For over three decades the site has succeeded in fostering a working environment where team members take pride in both the excellence of their personal and collective contributions and the positive benefits they provide to patients around the world. This is an opportunity to work for a household name and to grow...
27-11-2015 - jobsearch.ie save
 

Global Quality Auditor

Dublin - Experienced
Global Pharmaceutical Company looking for experienced Global Quality Auditors to join their team. Duties and Responsibilities: Provide objective audits of internal GXP systems and external businesses Management in order to accurately depict the status of compliance and to foster improvements based on current GXP references and interpretations. Prepare and conduct internal and external audits globally Perform independent research of required topics and FDA, EMEA, TGA, Health Canada, WHO, PIC/S, MHLW, and other national, international, or supranational regulations (GxP and ICH) including...
14-11-2015 - jobsearch.ie save
 

Regulatory Affairs Manager

Dublin
Regulatory Affairs Manager is required for a South Dublin based Biopharmaceutical company that specialises in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. In July 2015 the site opened a $300million investment, which added significantly to the sites laboratory, filling, packaging and distribution (including cold chain) capabilities. The site is a fast paced, collaborative, team based working environment, where you get an opportunity to work with other highly skilled staff in a strategically important site in the companies global supply chain. This role...
08-11-2015 - jobsearch.ie save
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