Job description

Duration: 3+ Months Job Description: 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. What You Will Do • 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. Education: • Bachelor’s degree in Science or Engineering. Experience • 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. Knowledge, Skills, and Abilities • 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. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com . US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.

Requirements

Must-haves

Duration: 3+ Months
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.
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.
Knowledge, Skills, and Abilities
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.

Nice-to-haves

None flagged.

Application prep

Use the role’s language and application details while tailoring your materials.

Keywords to mirror

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Effort: medium