18 Field Specialist QA Operations Jobs in Devens, MA
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SPECTRAFORCE is Hiring a Field Specialist QA Operations Near Devens, MA
Job Title: Field QA Specialist
Location: Devens, MA 01434
Duration: 12 Months
Local Candidates Only
Work Schedule is: 5AM - 5PM, 12 hour shift. Working A1 Crew.These are 12 hour shifts.
2 days on/2 days off---3 days on/2 days off
Weekends are included. Holidays included as the needs of the business warrant.Job SummarySeeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. The Contractor Field QA Specialist is responsible for quality activities for the LSCC in accordance with Company policies, standards, procedures, and Global cGMP.
Job Responsibilities
Equal Opportunity Employer: SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at LOA@spectraforce.com if you require reasonable accommodation.
Location: Devens, MA 01434
Duration: 12 Months
Local Candidates Only
Work Schedule is: 5AM - 5PM, 12 hour shift. Working A1 Crew.These are 12 hour shifts.
2 days on/2 days off---3 days on/2 days off
Weekends are included. Holidays included as the needs of the business warrant.Job SummarySeeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. The Contractor Field QA Specialist is responsible for quality activities for the LSCC in accordance with Company policies, standards, procedures, and Global cGMP.
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.
- High School Degree required
- Relevant college or university degree preferred.
- Minimum 4 years relevant work experience, with experience in a Quality Assurance role.
- 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. About Us: Established in 2004, SPECTRAFORCE® is one of the largest and fastest-growing diversity-owned staffing firms in the US. The growth of our company is a direct result of our global client service delivery model that is powered by our state-of-the-art A.I. proprietary talent acquisition platform, robust ISO 9001:2015/ISO 27001 certified processes, and strong and passionate client engaged teams. We have built our business by providing talent and project-based solutions, including Contingent, Permanent, and Statement of Work (SOW) services to over 140 clients in the US, Canada, Puerto Rico, Costa Rica, and India. Key industries that we service include Technology, Financial Services, Life Sciences, Healthcare, Telecom, Retail, Utilities and Transportation. SPECTRAFORCE is built on a concept of “human connection,” defined by our branding attitude of NEWJOBPHORIA®, which is the excitement of bringing joy and freedom to the work lifestyle so our people and clients can reach their highest potential. Learn more at: http://www.spectraforce.com
Equal Opportunity Employer: SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at LOA@spectraforce.com if you require reasonable accommodation.
Job Summary
JOB TYPE
Full Time
SALARY
$80k-99k (estimate)
POST DATE
06/05/2024
EXPIRATION DATE
07/03/2024
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