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Technical Writer
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineering, Support
Projektbeschreibung
ROLE - TECHNICAL WRITER
TYPE - INITIALLY 6 MONTH CONTRACT
LOCATION - CO. LIMERICK
PROFILE
One of our key global Biopharmaceutical clients are heavily investing in a new facility and are in a need of a capable Technical Writer to look after the documents for Process Qualification, Process Validation and Developmental Studies.
KEY RESPONSIBILITIES:
- Writing and creating of protocols for Process Qualification campaign, Process Validation Campaign and Developmental Studies.
- Writes and creates reports for Process Qualification campaign, Process Validation Campaign and Developmental Studies.
- Performs Data verification for studies and reports.
- Ensure consistency of content, format, layouts of all related protocols and reports.
- Edit, standardise, or make changes to material prepared by other writers or establishment personnel.
- Assists MFG Support investigations by documenting in writing investigations of process deviations.
- Assists in the review/approval process for protocols and reports through paper based or electronic systems.
- Writes, reviews, and maintains department standard operating procedures.
- Proficient in Microsoft applications such as Word, Excel, Powerpoint and Project.
- Experience in document systems would be beneficial
- Experience in GMP systems would be beneficial
- Resolves problems, identifies issues and determines system improvements
- Attend meetings relevant to assigned projects as needed.
- Other related duties as assigned.
Key Experience:
- BS/BA degree in science, engineering, or related discipline
- Experience in writing and/or editing technical documents.
- Experience with GMP systems would be beneficial. Will substitute relevant writing experience in lieu of degree.
TYPE - INITIALLY 6 MONTH CONTRACT
LOCATION - CO. LIMERICK
PROFILE
One of our key global Biopharmaceutical clients are heavily investing in a new facility and are in a need of a capable Technical Writer to look after the documents for Process Qualification, Process Validation and Developmental Studies.
KEY RESPONSIBILITIES:
- Writing and creating of protocols for Process Qualification campaign, Process Validation Campaign and Developmental Studies.
- Writes and creates reports for Process Qualification campaign, Process Validation Campaign and Developmental Studies.
- Performs Data verification for studies and reports.
- Ensure consistency of content, format, layouts of all related protocols and reports.
- Edit, standardise, or make changes to material prepared by other writers or establishment personnel.
- Assists MFG Support investigations by documenting in writing investigations of process deviations.
- Assists in the review/approval process for protocols and reports through paper based or electronic systems.
- Writes, reviews, and maintains department standard operating procedures.
- Proficient in Microsoft applications such as Word, Excel, Powerpoint and Project.
- Experience in document systems would be beneficial
- Experience in GMP systems would be beneficial
- Resolves problems, identifies issues and determines system improvements
- Attend meetings relevant to assigned projects as needed.
- Other related duties as assigned.
Key Experience:
- BS/BA degree in science, engineering, or related discipline
- Experience in writing and/or editing technical documents.
- Experience with GMP systems would be beneficial. Will substitute relevant writing experience in lieu of degree.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges