Technical Writer

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, operational agendas, and cross-functional projects.

• 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.

• 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.

• Bachelor’s degree in Science or Engineering.
• 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.

The role involves working in a collaborative, fast-paced manufacturing environment where attention to detail and adherence to quality standards are paramount. The position requires proficiency in using internal software systems such as ERP, Enterprise Quality Management Systems, and Document Management Systems. The Technical Writer will interact closely with cross-functional teams and should be comfortable with managing multiple projects simultaneously.

This is a Contract position based out of Carlsbad, CA.

The pay range for this position is $33.00 - $33.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Carlsbad,CA.

This position is anticipated to close on Mar 5, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $33