Field Specialist QA Operations - Unlimited Growth Potential

Please note: the work schedule is Mon - Fri 2PM - 10PM EST
However, before the person starts that schedule they are required to complete Training and Integration Period.
This is 8 - 10 weeks on 1st shift which is 7AM - 3:30PM Mon - Fri
Please be sure candidates understand and can work this schedule for this time period, and then be available to move to the 2nd shift work schedule.
This role is 100% Onsite
Work Schedule: Mon - Fri, 2PM - 10PM EST

JOB SUMMARY
Client is seeking a Contractor Field QA Specialist for the QA Operations organization at the Single Use Facility (SUF) in Devens, MA. The Contractor Field QA Specialist is responsible for quality activities for the Single Use Facility in accordance with Client policies, standards, procedures, and Global cGMP. Functional responsibilities include ensuring manufacturing compliance with applicable procedures and batch records, providing real time review of manufacturing batch record documentation and logbooks, and working with operations to resolve manufacturing issues. The Contractor Field QA Specialist role is stationed in Devens, MA and reports to the Senior Manager of QA Operations for the Devens SUF.

This role is Monday through Friday 2pm - 10:30pm

JOB RESPONSIBILITIES
" Perform QA on the floor activities.
" Ensure manufacturing compliance with applicable procedures and batch records.
" Perform real time review of manufacturing batch records.
" Review manufacturing shop floor documentation.

EDUCATION REQUIREMENTS
" High School Degree required
" Relevant college or university degree preferred.
" Minimum 4 years relevant work experience, with experience in a Quality Assurance role.

QUALIFICATIONS REQUIRED
" Equivalent combination of education and experience acceptable.
" Must be action-oriented and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking.
" Understands continuous improvement and improves efficiency and productivity within the group or project.
" Builds relationships internally within and with cross functional teams.
" Must have sound knowledge and experience in FDA regulated cGMP warehousing, Quality, and compliance environments. Prefer to also have knowledge of GMP Manufacturing operations and processes.
" Directs quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies.
" Routinely recognizes and resolves Quality issues; Informs management of proposed solutions. Seeks management guidance on complex issues.
" Able to recognize conflict and notify management with proposed recommendations for resolution.
" Must possess an independent mindset. Work is self-directed.
" Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision.
" Confident in making decisions for non-routine issues.
" Develops and revises procedures.
" Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution.
" Able to prepare written communications and communicate problems to management with clarity and accuracy.
" Able to effectively multi-task.
" Knowledge of US and global cGMP requirements.
Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles.
" Must be skilled in planning and organizing, decision-making, and building relationships.
" Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management.
" Able to effectively multi-task.
" Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality Risk Management principles.
" Must be skilled in planning and organizing, decision-making, and building relationships.
" Knowledge of quality processes, change control, product complaints, deviations, investigations, and CAPA management.