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Technical Writer
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Technical Writer

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1 Vacancy
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Jobs by Experience

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1-3 years

Job Location

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Dublin - Ireland

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1759490

About PSC Biotech


Who we are?
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.


Take your Career to a new Level
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.


Employee Value Proposition
Employees are the heartbeat of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.


Description:

Overview: The activities performed in the role of Technical Writer include:

  • Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures.
  • Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.
  • Develop protocols for execution in Manufacturing & Inspection in support of change controls, deviations & troubleshooting investigations with support from relevant SMEs.
  • Involvement in projects as part of continuous process improvement and / or troubleshooting,
  • Ownership of change controls for Manufacturing/Inspection/Engineering.
  • Issuance and updates of paper batch records in line with production schedule.
  • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS.
  • Support production support team in reducing document turnaround times.
  • Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.
  • Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs.
  • Ownership of minor deviations as required.


Requirements


Basic Qualifications:

  • Educated to degree level or equivalent.
  • Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation.



#LI-BR1

Basic Qualifications: Educated to degree level or equivalent. Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation. #LI-BR1

Employment Type

Full Time

Company Industry

About Company

0-50 employees
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