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 ...
Aequor Technologies
66 jobs near Columbus, OH
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 ...
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 ...
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 ...
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 ...
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 ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
Partnering cross-functionally with Manufacturing, QC, and Engineering teams Identifying opportunities for continuous improvement and operational excellence Acting as a quality advocate, promoting a ...
SAS Programmer
East Brunswick, NJ · On-site
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
SAS Programmer
East Brunswick, NJ · On-site
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
SAS Programmer
East Brunswick, NJ · On-site +1
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
SAS Programmer
East Brunswick, NJ · On-site +1
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
SAS Programmer
Oakland, CA · On-site
Aditi is an IT consulting firm that specializes in providing premium technology solutions across a ... line at 650-458-5456 SAS Developer Oakland, CA 6 months Contract Description Need to know ...
SAS Programmer
Oakland, CA · On-site
Aditi is an IT consulting firm that specializes in providing premium technology solutions across a ... line at 650-458-5456 SAS Developer Oakland, CA 6 months Contract Description Need to know ...
SAS Programmer
Philadelphia, PA · On-site
Company Description SA Technologies Inc. (www.satincorp.com) is a market leader and one of the ... Minimum three years' experience in BASE SAS products and procedures and one year experience in ...
SAS Programmer
Philadelphia, PA · On-site
Company Description SA Technologies Inc. (www.satincorp.com) is a market leader and one of the ... Minimum three years' experience in BASE SAS products and procedures and one year experience in ...
Company Information Clinical Ink is the global life science company that brings data, technology ... Clinical Ink is seeking a SAS Programmer to join our Data Management team based remotely across the ...
Company Information Clinical Ink is the global life science company that brings data, technology ... Clinical Ink is seeking a SAS Programmer to join our Data Management team based remotely across the ...
Clinical SAS Programmer
Chantilly, VA · Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education: Bachelor's degree in Computer Science, Computer Engineering, or related technical field Job Summary ...
Quick apply
Clinical SAS Programmer
Chantilly, VA · Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education: Bachelor's degree in Computer Science, Computer Engineering, or related technical field Job Summary ...
SAS Programmer
Eagan, MN · On-site
... complete technology services in Mobile development, Web development, Cloud computing and ... We use Objective C and Swift programming languages to create native applications for iPhone ...
SAS Programmer
Eagan, MN · On-site
... complete technology services in Mobile development, Web development, Cloud computing and ... We use Objective C and Swift programming languages to create native applications for iPhone ...
Company Description Global Channel Management is a technology company that specializes in various ... Requires time management skills, and strong SAS programming expertise. Reviews case report form ...
Company Description Global Channel Management is a technology company that specializes in various ... Requires time management skills, and strong SAS programming expertise. Reviews case report form ...
Company Description Established in 1991, Collabera has been a leader in IT staffing for over 22 ... Programmer SAS Location: Abbott Park, IL, 60064 Responsibilities: SAS developer with 10+ year ...
Company Description Established in 1991, Collabera has been a leader in IT staffing for over 22 ... Programmer SAS Location: Abbott Park, IL, 60064 Responsibilities: SAS developer with 10+ year ...
... technologies and program management solutions. Our methods include- applying domain expertise in ... Job Title: Sr. SAS Programmer Analyst Duration: 1 year+ Location : Woodcliff Lake, NJ * Perform SAS ...
... technologies and program management solutions. Our methods include- applying domain expertise in ... Job Title: Sr. SAS Programmer Analyst Duration: 1 year+ Location : Woodcliff Lake, NJ * Perform SAS ...
Company Description Global Channel Management is a technology company that specializes in various ... Qualifications Performs all SAS programming required for clinical trial analysis and reporting.
Company Description Global Channel Management is a technology company that specializes in various ... Qualifications Performs all SAS programming required for clinical trial analysis and reporting.
SAS Programmer
New York, NY · On-site
Yes • Resources with SAS skill sets and actuarial background. • Should be good in understanding the existing SAS programs and reverse engineer the logic for building it in new technology. • ...
SAS Programmer
New York, NY · On-site
Yes • Resources with SAS skill sets and actuarial background. • Should be good in understanding the existing SAS programs and reverse engineer the logic for building it in new technology. • ...
SAS Programmer
Eagan, MN · On-site
... complete technology services in Mobile development, Web development, Cloud computing and ... We use Objective C and Swift programming languages to create native applications for iPhone ...
SAS Programmer
Eagan, MN · On-site
... complete technology services in Mobile development, Web development, Cloud computing and ... We use Objective C and Swift programming languages to create native applications for iPhone ...
Senior SAS Programmer
Okemos, MI · On-site
Senior SAS Programmer Location: Hybrid - Okemos, MI (Minimum 2 days onsite weekly; moving to 3 days/week soon) · We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work ...
Quick apply
Senior SAS Programmer
Okemos, MI · On-site
Senior SAS Programmer Location: Hybrid - Okemos, MI (Minimum 2 days onsite weekly; moving to 3 days/week soon) · We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work ...
Full-time
This job post has expired 2 days ago. Applications are no longer accepted.
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