Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current ... Or Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or ...
62 Aequor Technologies Quality Assurance Associate Jobs Hiring Near You
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current ... Or Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or ...
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current ... Or Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or ...
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current ... Or Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or ...
QA Associate
Fishers, IN · On-site
The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...
QA Associate
Fishers, IN · On-site
The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting ... Quality Assurance Associate. Location: Winchester, KY. Description: * A QA Associate must be ...
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting ... Quality Assurance Associate. Location: Winchester, KY. Description: * A QA Associate must be ...
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting ... Quality Assurance Associate Location: Winchester, KY. Description: * A QA Associate must be ...
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting ... Quality Assurance Associate Location: Winchester, KY. Description: * A QA Associate must be ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Quality Assurance Associate
Houston, TX · On-site
$22/hr
... technology • Thrive in a company that values a culture of safety to include top-notch safety ... QA Associates • Monitors quality of plant utility samples as requested • Maintain good ...
Quality Assurance Associate
Houston, TX · On-site
$22/hr
... technology • Thrive in a company that values a culture of safety to include top-notch safety ... QA Associates • Monitors quality of plant utility samples as requested • Maintain good ...
Quality Assurance Associate
Houston, TX · On-site
$22/hr
... technology • Thrive in a company that values a culture of safety to include top-notch safety ... QA Associates • Monitors quality of plant utility samples as requested • Maintain good ...
Quality Assurance Associate
Houston, TX · On-site
$22/hr
... technology • Thrive in a company that values a culture of safety to include top-notch safety ... QA Associates • Monitors quality of plant utility samples as requested • Maintain good ...
Quality Assurance Associate
San Diego, CA · On-site
$24 - $33/hr
Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The Quality Assurance Associate supports the effective operation of the Quality Management System through ...
Quality Assurance Associate
San Diego, CA · On-site
$24 - $33/hr
Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The Quality Assurance Associate supports the effective operation of the Quality Management System through ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
The QA Associate will also be providing local internal and external audit support at our Newtown, PA location. This position offers an excellent opportunity for recent graduates or early-career ...
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The QA Associate will also be providing local internal and external audit support at our Newtown, PA location. This position offers an excellent opportunity for recent graduates or early-career ...
Quality Assurance Associate
San Diego, CA · On-site
$24 - $33/hr
Quality Assurance Associate - Document Control, Training, and Asset ManagementJob PurposeThe Quality Assurance Associate supports the effective operation of the Quality Management System through ...
Quick apply
Quality Assurance Associate
San Diego, CA · On-site
$24 - $33/hr
Quality Assurance Associate - Document Control, Training, and Asset ManagementJob PurposeThe Quality Assurance Associate supports the effective operation of the Quality Management System through ...
Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The Quality Assurance Associate supports the effective operation of the Quality Management System through ...
Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The Quality Assurance Associate supports the effective operation of the Quality Management System through ...
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QA Associate
Quakertown, PA · On-site
$900 - $1.4K/wk
We are seeking a QA Associate to become an integral part of our team! Responsibilities: * Maintains ... Ability to Multi Task Company Description Particle Size Technology Inc recognizes that the ...
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QA Associate
Quakertown, PA · On-site
$900 - $1.4K/wk
We are seeking a QA Associate to become an integral part of our team! Responsibilities: * Maintains ... Ability to Multi Task Company Description Particle Size Technology Inc recognizes that the ...
Be Seen First
QA Associate
Quakertown, PA · On-site
$900 - $1.4K/wk
We are seeking a QA Associate to become an integral part of our team! Responsibilities: * Maintains ... Ability to Multi Task Company Description Particle Size Technology Inc recognizes that the ...
Quick apply
Be Seen First
QA Associate
Quakertown, PA · On-site
$900 - $1.4K/wk
We are seeking a QA Associate to become an integral part of our team! Responsibilities: * Maintains ... Ability to Multi Task Company Description Particle Size Technology Inc recognizes that the ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Job Title: QA Associate Location: Winchester, KY Duration:6 months Contract on W2 (Temp-to-Hire) SHIFT: MON to FRI 2 PM to 10:30 PM Description: A QA Associate must be familiar with applicable GMP ...
Quality Assurance Associate
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in addition to the review of controlled documents (both executed and unexecuted) in accordance with ...
Quality Assurance Associate
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in addition to the review of controlled documents (both executed and unexecuted) in accordance with ...
Quality Assurance Associate
Winchester, KY · On-site
$24 - $26/hr
Quality Assurance Associate Location: Winchester, KY 40391 TEMP TO HIRE - DURATION - 6 MONTHS ONSITE POSITION - SHIFT - FRI, SAT, SUN 6PM - 6AM + 1 DAY EVERY OTHER WEEK + MANDATORY OVERTIME.
Quick apply
Quality Assurance Associate
Winchester, KY · On-site
$24 - $26/hr
Quality Assurance Associate Location: Winchester, KY 40391 TEMP TO HIRE - DURATION - 6 MONTHS ONSITE POSITION - SHIFT - FRI, SAT, SUN 6PM - 6AM + 1 DAY EVERY OTHER WEEK + MANDATORY OVERTIME.
Quality Assurance Associate
Newtown, PA · On-site
The QA Associate will also be providing local internal and external audit support at our Newtown, PA location. This position offers an excellent opportunity for recent graduates or early-career ...
Quality Assurance Associate
Newtown, PA · On-site
The QA Associate will also be providing local internal and external audit support at our Newtown, PA location. This position offers an excellent opportunity for recent graduates or early-career ...
Aequor Technologies Jobs Information
What makes Aequor Technologies an attractive place to work?
Aequor Technologies is a cutting-edge biotechnology company that has established itself as a leader in the field of bioluminescence and fluorescence technologies. The company's workplace is characterized by a culture of innovation, collaboration, and open communication, where employees are encouraged to think creatively and work together to drive scientific breakthroughs. Joining Aequor Technologies offers opportunities for professionals to contribute to groundbreaking research, develop new skills, and advance their careers in a dynamic and supportive environment.
What other companies are hiring for Quality Assurance Associate jobs?
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What are the most popular categories at Aequor Technologies?
Job description
Fully Onsite - occasional flexibility to WFH (1-2 days per week after 6 months) - standard working hours 8 AM - 5 PM
Ideal candidate: B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience.
What you will do
In this role you will support the manufacturing team and provide technical expertise to regularly draft and revise documents such as Standard Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP regulated environment that supports the manufacturing process.
Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team.
Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents.
Liaise with manufacturing team and other cross functional departments regarding documentation changes in an effective and timely manner.
Collaborate with multiple departments to support new/revise training documentation for manufacturing staff.
Support process owners and participate in continuous process improvement and / or troubleshooting projects.
Support manufacturing team in reducing document turnaround times.
Ensure documentation related actions are completed on time and current schedule is maintained, accurate, and up to date.
Develop protocols for Manufacturing to support change controls, deviations & troubleshooting investigations with provision from relevant SMEs.
Generate, own, and provide subject matter expertise to Quality System records as minor deviations, CAPA and change control records.
Track pending activities required to support change control implementations.
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current operating systems.
Share knowledge with members of the manufacturing team.
Basic Qualifications:
Master's Degree in Science and/or Engineering.
Or
Bachelor's Degree in Science and/or Engineering and 2 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Or
Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Or
High School Diploma / GED and 8 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Preferred Qualifications:
Educational Background in Science and/or Engineering.
Experience working in GMP pharma and/or biotechnology industry.
Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing.
Experience with device assembly and packaging of final product.
Ability to translate highly technical information into easily understandable information for manufacturing operators.
Dynamic skills and usage of photographs, drawings, diagrams, animation, and charts that increase users' understanding.
Experience supporting deviations, investigations, CAPA's and change controls.
A fact-based problem solver with strong troubleshooting and problem-solving skills.
Pro-active with the ability to prioritize work to meet benchmarks
Good documentation and communication
Ideal candidate: B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience.
What you will do
In this role you will support the manufacturing team and provide technical expertise to regularly draft and revise documents such as Standard Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP regulated environment that supports the manufacturing process.
Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team.
Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents.
Liaise with manufacturing team and other cross functional departments regarding documentation changes in an effective and timely manner.
Collaborate with multiple departments to support new/revise training documentation for manufacturing staff.
Support process owners and participate in continuous process improvement and / or troubleshooting projects.
Support manufacturing team in reducing document turnaround times.
Ensure documentation related actions are completed on time and current schedule is maintained, accurate, and up to date.
Develop protocols for Manufacturing to support change controls, deviations & troubleshooting investigations with provision from relevant SMEs.
Generate, own, and provide subject matter expertise to Quality System records as minor deviations, CAPA and change control records.
Track pending activities required to support change control implementations.
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current operating systems.
Share knowledge with members of the manufacturing team.
Basic Qualifications:
Master's Degree in Science and/or Engineering.
Or
Bachelor's Degree in Science and/or Engineering and 2 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Or
Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Or
High School Diploma / GED and 8 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Preferred Qualifications:
Educational Background in Science and/or Engineering.
Experience working in GMP pharma and/or biotechnology industry.
Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing.
Experience with device assembly and packaging of final product.
Ability to translate highly technical information into easily understandable information for manufacturing operators.
Dynamic skills and usage of photographs, drawings, diagrams, animation, and charts that increase users' understanding.
Experience supporting deviations, investigations, CAPA's and change controls.
A fact-based problem solver with strong troubleshooting and problem-solving skills.
Pro-active with the ability to prioritize work to meet benchmarks
Good documentation and communication
About Aequor Technologies
Sourced by ZipRecruiter
Aequor Technologies, located in Piscataway, New Jersey, is an established IT consulting and solutions company that operates primarily in the United States. The company, founded in 1998, specializes in providing high-value, cost-effective IT services and solutions for a variety of industries, including health care, life sciences, manufacturing, and media and entertainment. They offer a wide array of services including IT consulting, application development, infrastructure management, and strategic staffing solutions. Its mission is to facilitate its clients in their pursuit of achieving business objectives through effective and efficient use of technology. Aequor Technologies is a significant player in its field, boasting several accomplishments including repeated recognition as one of the fastest growing privately-held companies in the U.S. by Inc. 5000.
Industry
Recruiting and staffing services
Company size
201 - 500 Employees
Headquarters location
Piscataway, NJ, US
Year founded
1998