Author Jobs

Headcount Solutions Limited - Dublin, Dublin City

and interpretation. * Author and review standard operating procedures and technical reports * Supporting multidisciplinary teams (MS&T, quality, analytics, regulatory) for process improvement and troubleshooting

from: CV-library.ie (+1 source) - 14 days ago

BioMarin International Limited - Cork

Author documentation summarizing reportable changes to analytical methods Support the authoring and review of the CTD Module 3 DS and DP sections for INDs, IMPDs, BLAs, MAAs etc. Author RTQs for methods 12000.0

from: irishjobs.ie - Yesterday

Amgen - Dublin

release to ensure GMP compliance. Negotiator, author and Approver of quality agreements Lead the preparation of the site for and Represent Amgen at product-specific Regulatory Inspections and/or during 12000.0

from: irishjobs.ie - 4 days ago

CPL Recruitment - Dublin

markets/localisation projects. Liaise with customers both internal and external to support overall method transfer processes. Provide technical support to all new country launches. Technical author, review Negotiable

from: cpljobs.com - 22 days ago

Embecta - Dublin

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships 12000.0

from: irishjobs.ie - 6 days ago

Life Science Recruitment Ltd - Carlow

in validation of sterile fill finish processes and equipment and a relevant degree Responsibilities Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies 26000.0

from: irishjobs.ie - 7 days ago

PSC Biotech Ltd - Carlow, Ireland

Shift Pattern: Candidates must be flexible to be available to work shifts as may be required (2 Cycle 5 days a week: 7am-3pm and 3pm-11pm) Requirements Role Functions: Design/Author/Review/Approve/Execute

from: zoho.eu - More than 30 days ago

Life Science Recruitment Ltd - Carlow

extensive cleaning validation experience Responsibilities Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process 26000.0

from: irishjobs.ie - 7 days ago

BioMarin International Limited - Cork

and interpret and present results Clear technical writing and editing to author or oversee generation of technical reports Successful management of scientists, with focus on professional development for employee 12000.0

from: irishjobs.ie - Yesterday

PSC Biotech Ltd - Carlow, Ireland

to carry out the following: Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process. Design/Author/Review/Approve

from: zoho.eu - More than 30 days ago