Field Specialist QA Operations - Sunrise Systems Inc
Devens, MA 01434
About the Job
Job Title: Field QA Specialist
Job ID: 24-04229
Location: Devens, MA, 01434
Duration: 12 Months contract on W2
This role is 100% Onsite
Work Schedule: Mon - Fri, 2:00 PM - 10:30 PM 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
Job ID: 24-04229
Location: Devens, MA, 01434
Duration: 12 Months contract on W2
This role is 100% Onsite
Work Schedule: Mon - Fri, 2:00 PM - 10:30 PM 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.
Additional Information:
No requirements for lifting or driving equipment
No exposure to hazardous materials
Contact
Satya S | Direct: (732) 272-0262 | Email: satya@sunrisesys.com | URL: www.sunrisesys.com
No requirements for lifting or driving equipment
No exposure to hazardous materials
Contact
Satya S | Direct: (732) 272-0262 | Email: satya@sunrisesys.com | URL: www.sunrisesys.com
Source : Sunrise Systems Inc
