Manufacturing Excellence/ Technical Writer/ Deviation Writing/ Manufacturing Expert/ Deviation Writer

Roles & ResponsibilitiesSummary· The company is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team.· This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations.· The Deviation Writer will work closely with the Manufacturing, Production...

Roles & ResponsibilitiesSummary· The company is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team.· This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations.· The Deviation Writer will work closely with the Manufacturing, Production...

Roles & ResponsibilitiesSummary· The company is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team.· This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations.· The Deviation Writer will work closely with the Manufacturing, Production...

Roles & ResponsibilitiesSummary· The company is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team.· This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations.· The Deviation Writer will work closely with the Manufacturing, Production...

Roles & ResponsibilitiesThe Deviation investigator Writer is responsible for the initiation, investigation and completion of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. The position is expected to work in a cGMP environment, have working knowledge of Biopharmaceutical manufacturing...

Roles & ResponsibilitiesThe Deviation investigator Writer is responsible for the initiation, investigation and completion of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. The position is expected to work in a cGMP environment, have working knowledge of Biopharmaceutical manufacturing...

Roles & ResponsibilitiesEssential Functions· Utilize technical writing strategies to ensure content of documentation is clear, concise, and complete.· Author and revise technical documentation including facility and equipment SOPs, batch records, specifications, and training documents.· Author and manage change controls as necessary to implement new...

Roles & ResponsibilitiesEssential Functions· Utilize technical writing strategies to ensure content of documentation is clear, concise, and complete.· Author and revise technical documentation including facility and equipment SOPs, batch records, specifications, and training documents.· Author and manage change controls as necessary to implement new...

Job SummaryWe are seeking an experienced Deviation Writer to join our Manufacturing Engineering team in a regulated GMP environment. The ideal candidate will possess strong technical writing skills, excellent interpersonal abilities, and a deep understanding of industry-standard electronic Quality Management Systems.This is a critical role that requires the...

Job DescriptionWe are seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team.The ideal candidate will have a strong background in technical writing, excellent organizational skills, and the ability to work effectively with cross-functional teams.The role is crucial for translating complex technical events into...

Roles & ResponsibilitiesNo Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We...

Roles & ResponsibilitiesYour Responsibilities· Ensures Master Production Records (MPRs), Production Summaries (PS), and Master Cleaning Records (MCR) are drafted in such a manner that clearly describes the process and captures all data required in Sterling’s format and a cGMP compliant manner based on a detailed Technical Package from the Development Team...

Roles & ResponsibilitiesYour Responsibilities· Ensures Master Production Records (MPRs), Production Summaries (PS), and Master Cleaning Records (MCR) are drafted in such a manner that clearly describes the process and captures all data required in Sterling’s format and a cGMP compliant manner based on a detailed Technical Package from the Development Team...

Deviation Investigation Intern Apply locations SG - Tuas, Singapore Time type: Full time Posted on: Posted 27 Days Ago Job requisition id: R63226 Lonza is a global leader in life sciences. The Singapore site is a mammalian cell culture manufacturing facility for the contract development and production of multiple biopharmaceutical products, including...

We are seeking an experienced Manufacturing Operations Specialist to join our team at No Deviation PTE. LTD.As a key member of our operations team, you will be responsible for ensuring the smooth execution of plant operations and supporting manufacturing processes.The successful candidate will possess strong technical skills and experience in...

NUSANTARA PRIME CONSULTING PTE. LTD. **Job Summary:**We are seeking an experienced Biotechnology Investigator Writer Specialist to join our team. The successful candidate will be responsible for conducting thorough investigations, identifying root causes, and implementing corrective actions to prevent recurrence in a cGMP environment. This role requires...

Instructional Designer and Technical Writer Next Labs is the leading provider of policy-driven information risk management (IRM) software for large enterprises, providing an exciting opportunity for Instructional Designer/Technical Writers to collaborate with highly talented product development teams in producing documentation for the next generation data...

Roles & ResponsibilitiesResponsible for the initiation, investigation and completion of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. The position is expected to work in a cGMP environment, have working knowledge of Biopharmaceutical manufacturing processes, the ability to manage...

Roles & ResponsibilitiesResponsible for the initiation, investigation and completion of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. The position is expected to work in a cGMP environment, have working knowledge of Biopharmaceutical manufacturing processes, the ability to manage...

Deviation Investigation Intern Apply locations SG - Tuas, Singapore Time type: Full time Posted on: Posted 27 Days Ago Job requisition id: R63226Lonza is a global leader in life sciences. The Singapore site is a mammalian cell culture manufacturing facility for the contract development and production of multiple biopharmaceutical products, including...