What are the responsibilities and job description for the Technical Operations Lead position at Intelliswift - An LTTS Company?
Title: Deviation Technical Writer
This 12-month position focuses on investigating and resolving manufacturing deviations to ensure quality and compliance.
Key Responsibilities:
• Investigate manufacturing deviations to determine root cause, recommend corrective/preventative actions, assess product impact, and summarize findings in writing.
• Collaborate with cross-functional teams to implement process improvements, streamline operations, and increase efficiency.
• Develop technical expertise in process and product knowledge through training and hands-on experience.
• Author and update technical documents, including investigations, process design, engineering studies, and change control.
Requirements:
• Bachelor's degree in Engineering or Sciences;
• Minimum one year of experience in a GMP manufacturing environment or equivalent combination of education and experience;
• Strong communication, collaboration, and problem-solving skills;
• Experience with technical writing, investigative tools, and vaccine manufacturing is preferred.
We are seeking a detail-oriented and analytical individual to join our team as a Deviation Technical Writer. If you have a passion for quality, compliance, and continuous improvement, we encourage you to apply.
This 12-month position focuses on investigating and resolving manufacturing deviations to ensure quality and compliance.
Key Responsibilities:
• Investigate manufacturing deviations to determine root cause, recommend corrective/preventative actions, assess product impact, and summarize findings in writing.
• Collaborate with cross-functional teams to implement process improvements, streamline operations, and increase efficiency.
• Develop technical expertise in process and product knowledge through training and hands-on experience.
• Author and update technical documents, including investigations, process design, engineering studies, and change control.
Requirements:
• Bachelor's degree in Engineering or Sciences;
• Minimum one year of experience in a GMP manufacturing environment or equivalent combination of education and experience;
• Strong communication, collaboration, and problem-solving skills;
• Experience with technical writing, investigative tools, and vaccine manufacturing is preferred.
We are seeking a detail-oriented and analytical individual to join our team as a Deviation Technical Writer. If you have a passion for quality, compliance, and continuous improvement, we encourage you to apply.
