Description:Summary:The Quality Document Technician is responsible for various assignments supporting the client quality systems and ensuring that required documents are created and organized for use in manufacturing and for releasing products.What you'll be doing:Makes detailed observations, analyzes data, and interprets results.Create, verify, and distribute quality documentation required for manufacturing.Support Document Center Technicians with standard office work and for batch release.Maintains department equipment and inventory levels for controlled materials.Identifies process improvements and escalates to Quality Supervision and/or Management.Ability to work independently and as part of a team in a fast-paced environment. What you'll bring:Basic science, math, and computer skills (including Microsoft Word and Excel) are required.Good writing, verbal communication, and problem-solving skills are required.Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements.It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities.The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.The ability to work on some weekends is required.Will work in both Drug Delivery and Penicillin facilities as needed.Overtime may be required to meet the production schedule. The candidate must not be allergic to penicillin or cephalosporin drugs6 months of experience in manufacturing/quality preferredHS Diploma or equivalent is requiredBasic science, math, and digital literacy (including Microsoft Word and Excel) are required.Strong writing and verbal communication abilities, as well as problem solving capabilities are needed.Attention to detail and organization are highly desiredIt is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in medical devices/pharma manufacturing facilities.Be able to work flexible hours in a dynamic environment with minimal direct supervision. Ability to work some Saturdays is required. Notes:This position is on-site VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status
Description:Summary:The Quality Document Technician is responsible for various assignments supporting the client quality systems and ensuring that required documents are created and organized for use in manufacturing and for releasing products.What you'll be doing:Makes detailed observations, analyzes data, and interprets results.Create, verify, and distribute quality documentation required for manufacturing.Support Document Center Technicians with standard office work and for batch release.Maintains department equipment and inventory levels for controlled materials.Identifies process improvements and escalates to Quality Supervision and/or Management.Ability to work independently and as part of a team in a fast-paced environment.
What you'll bring:Basic science, math, and computer skills (including Microsoft Word and Excel) are required.Good writing, verbal communication, and problem-solving skills are required.Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements.It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities.The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.The ability to work on some weekends is required.Will work in both Drug Delivery and Penicillin facilities as needed.Overtime may be required to meet the production schedule.
The candidate must not be allergic to penicillin or cephalosporin drugs6 months of experience in manufacturing/quality preferredHS Diploma or equivalent is requiredBasic science, math, and digital literacy (including Microsoft Word and Excel) are required.Strong writing and verbal communication abilities, as well as problem solving capabilities are needed.Attention to detail and organization are highly desiredIt is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in medical devices/pharma manufacturing facilities.Be able to work flexible hours in a dynamic environment with minimal direct supervision. Ability to work some Saturdays is required.
Notes:
This position is on-site
(Please ensure email matches your resume email)
(document types allowed: doc/docx/rtf/pdf/txt) (max 2MB)
By submitting this form, you are consenting to the VIVA team contacting you via Phone/Email