Technical Writer (Batch Record Review)

Varite, Inc

  • Carlsbad, CA
  • 7 days ago
  • $30–$33 Per Hour

Highlights

With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. 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.

Numbers & Facts

LocationCarlsbad, CA
Salary$30–$33 Per Hour

Description

VARITE is looking for qualified Technical Writer in Carlsbad, CA.
 
WHAT THE CLIENT DOES?
An American-headquartered life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.
 
WHAT WE DO?
Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.
 
Job Title: Technical Writer
Location: Carlsbad, CA
Contract Duration: 3 months
Pay Rate Range: $30.00 - $33.00/hr on W2
Work Authorization: Only USC or GC
 
HERE’S WHAT YOU’LL DO
Description:
How You Will Make an Impact

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.
 
How You Will Get Here
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.
 
BENEFITS:
We offer a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Eligible employees may receive:
  • Health Insurance: Medical, dental, and vision coverage
  • Retirement Plans: Participation in a company-sponsored retirement savings plan.
  • Legal Service Plans: Offering access to attorneys for legal advice and representation.
 
If this opportunity interests you, please respond by clicking on EasyApply.
 
Know someone who would be perfect for this role? Refer to us and if they are hired, you could be eligible for our employee referral bonus! Help us grow our team with top talent from your network.
VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Similar Jobs