Technical Writer (Deviations)

Technical Writer (Deviations)
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Technical Writer (Deviations)

Asia - Singapore
Industrial Engineering and Life-Science
Permanent
9/7/2026
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About the role

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Lead complex technical investigations into manufacturing deviations, non-conformances, and environmental excursions.
  • Utilize structured Root Cause Analysis (RCA) tools (e.g., Fishbone, 5 Whys, FMEA) to identify underlying triggers.
  • Author comprehensive investigation reports that withstand rigorous internal and external regulatory audits (FDA,EMA, etc.).
  • Perform impact assessments on product quality, safety, and efficacy.
  • Design and implement Corrective and Preventive Actions (CAPAs) to eliminate recurrence of deviations.
  • Monitor the effectiveness of implemented CAPAs through data-driven metrics.
  • Identify trends in manufacturing data to proactively suggest process improvements and "Right First Time" (RFT) initiatives.
  • Provide real-time engineering floor support to troubleshoot equipment malfunctions or process drift.
  • Collaborate with Quality Assurance (QA) and Production teams to ensure all activities align with Standard Operating Procedures (SOPs).
  • Participate in the drafting and revision of SOPs, Batch Records, and Validation protocols.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Lead complex technical investigations into manufacturing deviations, non-conformances, and environmental excursions.
  • Utilize structured Root Cause Analysis (RCA) tools (e.g., Fishbone, 5 Whys, FMEA) to identify underlying triggers.
  • Author comprehensive investigation reports that withstand rigorous internal and external regulatory audits (FDA,EMA, etc.).
  • Perform impact assessments on product quality, safety, and efficacy.
  • Design and implement Corrective and Preventive Actions (CAPAs) to eliminate recurrence of deviations.
  • Monitor the effectiveness of implemented CAPAs through data-driven metrics.
  • Identify trends in manufacturing data to proactively suggest process improvements and "Right First Time" (RFT) initiatives.
  • Provide real-time engineering floor support to troubleshoot equipment malfunctions or process drift.
  • Collaborate with Quality Assurance (QA) and Production teams to ensure all activities align with Standard Operating Procedures (SOPs).
  • Participate in the drafting and revision of SOPs, Batch Records, and Validation protocols.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Your profile

This is some text inside a div block.

Job Requirements:

  • Bachelor's degree in Science, Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or a related life science field
  • 2 years’ experience in Engineering, pharmaceutical industry
  • Strong understanding of cGMP, and global standards.
  • Experience with process flow diagrams, technical illustrations, and instructional design
  • Familiarity with Lean Manufacturing and Six Sigma principles.
  • Knowledge of digital documentation tools and content management systems (TrackWise, VeevaVault).
  • Strong documentation and technical writing skills.
  • Candidates must be highly motivated, able to work both independently and as part of a team, and possess strong organizational and verbal and written communication skills

About Antaes

Founded in 2007, Antaes is a Swiss management and technology consulting firm ranked among the top 15 consulting firms in Switzerland. We have more than 300 experienced engineers who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong, and France, we support our clients and international clients by providing services in the following areas:

  • Organizational and Transformation Consulting
  • Industrial Engineering
  • Information Systems Management

 

When you join our team, you’ll discover:

  • A dynamic team with a startup mindset
  • Personalized support and guidance as your career progresses
  • Challenges to help you grow your network
  • Events: team-building activities, meetups, workshops, Winter Event …
  • A company certified by @HappyAtWork with a strong commitment to CSR (Ecovadis Gold Medal 2023)

APPLY
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Technical Writer (Deviations)

Asia - Singapore
Industrial Engineering and Life-Science
Permanent

About the role

This is some text inside a div block.

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Lead complex technical investigations into manufacturing deviations, non-conformances, and environmental excursions.
  • Utilize structured Root Cause Analysis (RCA) tools (e.g., Fishbone, 5 Whys, FMEA) to identify underlying triggers.
  • Author comprehensive investigation reports that withstand rigorous internal and external regulatory audits (FDA,EMA, etc.).
  • Perform impact assessments on product quality, safety, and efficacy.
  • Design and implement Corrective and Preventive Actions (CAPAs) to eliminate recurrence of deviations.
  • Monitor the effectiveness of implemented CAPAs through data-driven metrics.
  • Identify trends in manufacturing data to proactively suggest process improvements and "Right First Time" (RFT) initiatives.
  • Provide real-time engineering floor support to troubleshoot equipment malfunctions or process drift.
  • Collaborate with Quality Assurance (QA) and Production teams to ensure all activities align with Standard Operating Procedures (SOPs).
  • Participate in the drafting and revision of SOPs, Batch Records, and Validation protocols.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Your profile

This is some text inside a div block.

Job Requirements:

  • Bachelor's degree in Science, Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or a related life science field
  • 2 years’ experience in Engineering, pharmaceutical industry
  • Strong understanding of cGMP, and global standards.
  • Experience with process flow diagrams, technical illustrations, and instructional design
  • Familiarity with Lean Manufacturing and Six Sigma principles.
  • Knowledge of digital documentation tools and content management systems (TrackWise, VeevaVault).
  • Strong documentation and technical writing skills.
  • Candidates must be highly motivated, able to work both independently and as part of a team, and possess strong organizational and verbal and written communication skills
Our positions are open to individuals who have been recognized as workers with disabilities. T&S Group promotes diversity and equality in the workplace. All qualified male and female candidates are considered for employment on an equal basis.

About Antaes

Founded in 2007, Antaes is a Swiss management and technology consulting firm ranked among the top 15 consulting firms in Switzerland. We have more than 300 experienced engineers who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong, and France, we support our clients and international clients by providing services in the following areas:

  • Organizational and Transformation Consulting
  • Industrial Engineering
  • Information Systems Management

 

When you join our team, you’ll discover:

  • A dynamic team with a startup mindset
  • Personalized support and guidance as your career progresses
  • Challenges to help you grow your network
  • Events: team-building activities, meetups, workshops, Winter Event …
  • A company certified by @HappyAtWork with a strong commitment to CSR (Ecovadis Gold Medal 2023)