Technical Writer

AGW; Carlsbad (CA); On-site; USD 28,000 - 45,000; Full time

Job summary

Aptask Global Workforce (AGW) is seeking a Technical Writer for a 3-month contract in Carlsbad, CA. You will join the Manufacturing Sciences team to support site operations by documenting investigations, preparing reports, and ensuring quality compliance while collaborating with cross-functional colleagues.

The role requires a Bachelor's degree in Science or Engineering, strong written and verbal communication, and familiarity with QA documentation, ERP/Quality systems, and Lean methods.

Qualifications

• Excellent written and verbal communication skills.
• Bachelor's degree in Science or Engineering.
• Experience reviewing manufacturing batch records for accuracy.
• Familiarity with Lean/CI methodologies or PPI tools.
• Ability to work with cross-functional teams and manage documentation.

Responsibilities

• Prepare investigation reports and root cause analyses per quality standards.
• Analyze production records to extract data and insights.
• Collaborate with manufacturing personnel to standardize document formats.
• Author comprehensive, compliant documentation with accuracy.
• Utilize ERP and quality systems to gather information for investigations.
• Meet weekly targets for investigation submissions with quality.

Skills

Excellent written and verbal comms

Attention to detail

Collaboration

Problem-solving

Time management

Project management

Cross-functional collaboration

Education

Bachelor's degree in Science or Engineering

Tools

Microsoft Office (Excel)

ERP systems

Enterprise Quality Management Systems

Document Management Systems

Job description

Carlsbad, CA Onsite Contract Starts 8/31/2026 Ends 11/29/2026

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Job Description

Aptask Global Workforce (AGW) is seeking a Technical Writer for a contract position with a Global Life Sciences Company located in Carlsbad, CA. This is a 3-month contract opportunity.

As a Technical Writer joining the Manufacturing Sciences team, you will play a key role on a cross‑functional team supporting site operations in problem‑solving, process implementation, and investigative management. Working both independently and collaboratively, you will provide critical support to manufacturing operations by addressing quality issues and contributing to key initiatives.

Responsibilities:

• Prepare investigation reports and root cause analyses in accordance with established quality standards
• Analyze historical production records and manufacturing documentation to extract relevant data and insights into current processes
• Collaborate closely with manufacturing personnel to determine optimal document formats and identify appropriate methods, protocols, and best practices to incorporate into procedural instructions
• Author thorough, accurate, and compliant investigation documentation while maintaining strict adherence to quality documentation standards
• Utilize internal software systems, including ERP, Enterprise Quality Management Systems, and Document Management Systems, to gather and analyze information for investigations
• Meet weekly targets for investigation submissions while maintaining high standards of accuracy and quality

Requirements:

• Bachelor's degree in Science or Engineering
• Experience reviewing and evaluating manufacturing batch records and related documentation for accuracy and completeness
• Familiarity with Practical Process Improvement (PPI) systems and tools, or equivalent Continuous Improvement/Lean methodologies
• Experience collaborating with cross-functional teams on projects of varying complexity
• Solid understanding of manufacturing processes and interdepartmental workflows
• Proficiency in Microsoft Office applications, particularly Excel
• Excellent written and verbal communication skills
• Ability to thrive in a fast‑paced, dynamic environment
• Highly detail-oriented with strong accuracy and precision in documentation
• Positive, professional attitude and strong collaborative mindset
• Results‑driven and data‑focused approach to work
• Understanding of manufacturing operational flows, including Antibody Purification, Conjugation, and immunoassay QC assays
• Strong project management and time management skills
• Proactive problem‑solving mindset with the ability to anticipate needs and identify effective solutions

Pay range:

up to $33.00 per hour

Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.

Aptask Global Workforce (AGW)

ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.

Benefits of working with ApTask Global Workforce include:

• Medical
• Vision
• Sick Pay (for applicable states/municipalities)

Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website https://www.agwtalent.com/.

ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

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