Quality Assurance Associate
Covington, KY · On-site +1
Quality control of Standard Operating Procedures (SOPs) ensuring consistency in formatting ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
Quality Assurance Associate
Covington, KY · On-site +1
Quality control of Standard Operating Procedures (SOPs) ensuring consistency in formatting ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
Quality control of Standard Operating Procedures (SOPs) ensuring consistency in formatting ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
Quality control of Standard Operating Procedures (SOPs) ensuring consistency in formatting ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
Senior Field Applications Specialist - Central Ky and TN
Lexington, KY · On-site +1
$40/hr
... biotechnology? At Beckman Coulter Diagnostics , one of Danaher's 15+ operating companies, our work ... Provide both onsite and remote phone support to customers for assay and QC related questions and ...
Senior Field Applications Specialist - Central Ky and TN
Lexington, KY · On-site +1
$40/hr
... biotechnology? At Beckman Coulter Diagnostics , one of Danaher's 15+ operating companies, our work ... Provide both onsite and remote phone support to customers for assay and QC related questions and ...
Quality Assurance Manager
Louisville, KY · Remote
$100K - $127K/yr
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
Quick apply
Quality Assurance Manager
Louisville, KY · Remote
$100K - $127K/yr
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
While this role is remote, travel to locations will be required (50% travel). At Wieland, we ... Bachelor's degree or equivalent experience. * 5+ years' experience in QA/QC within manufacturing ...
CEI Inspector
Lexington, KY · On-site +1
Inspects traffic control and helps contractors maintain workplace safety standards. * Creates ... Some overnight stays may be required for remote projects. Why You'll Thrive at Egis At Egis, you'll ...
CEI Inspector
Lexington, KY · On-site +1
Inspects traffic control and helps contractors maintain workplace safety standards. * Creates ... Some overnight stays may be required for remote projects. Why You'll Thrive at Egis At Egis, you'll ...
Program Manager
Fort Knox, KY · On-site +1
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
Program Manager
Fort Knox, KY · On-site +1
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
Program Manager
Fort Knox, KY · On-site +1
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
Program Manager
Fort Knox, KY · On-site +1
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
Sr Quality Manager
Lexington, KY · Remote
... change control processes. * Ensure compliance with 21 CFR Part 111 and applicable dietary ... Conduct on-site and remote GMP audits evaluating quality systems, documentation practices ...
Quick apply
Sr Quality Manager
Lexington, KY · Remote
... change control processes. * Ensure compliance with 21 CFR Part 111 and applicable dietary ... Conduct on-site and remote GMP audits evaluating quality systems, documentation practices ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... control, surveillance, guard force programs. * Support crisis management, incident response ...
Program Manager
Fort Knox, KY · Remote
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
Program Manager
Fort Knox, KY · Remote
... for remote personnel across multiple locations * Ensure all deliverables are submitted accurately and on time, including: * Monthly Status Reports (MSR) * Man-hour reports * Quality Control ...
You will need to QC the collateral and ensure that it is booked to the right General Ledger and ... This position may be eligible for remote work in select geographic locations, subject to approval ...
You will need to QC the collateral and ensure that it is booked to the right General Ledger and ... This position may be eligible for remote work in select geographic locations, subject to approval ...
As a Production Quality Coordinator, you will be conducting Quality Control for two areas of the ... This position may be eligible for remote work in select geographic locations, subject to approval ...
As a Production Quality Coordinator, you will be conducting Quality Control for two areas of the ... This position may be eligible for remote work in select geographic locations, subject to approval ...
Fire System Designer
Louisville, KY · On-site +1
Revises designs from feedback when received from the quality control reviewer of each project ... This position will report to the corporate office in Louisville, KY but remote applicants will be ...
Fire System Designer
Louisville, KY · On-site +1
Revises designs from feedback when received from the quality control reviewer of each project ... This position will report to the corporate office in Louisville, KY but remote applicants will be ...
Remote Quality Control Biotech information
What is a remote quality control biotech?
A Remote Quality Control Biotech job involves ensuring the quality, safety, and compliance of biotechnological products and processes while working remotely. Responsibilities may include reviewing data, conducting virtual audits, ensuring regulatory compliance, and collaborating with teams to maintain product integrity. Professionals in this role use digital tools to analyze laboratory results, monitor production processes, and document findings. Strong attention to detail, knowledge of industry regulations, and proficiency in data analysis are essential. This position is critical in maintaining high-quality biotech products while allowing flexibility through remote work.
What skills and qualifications are needed for a remote quality control biotech?
To thrive as a Remote Quality Control Biotech, you generally need a solid background in biology or biotechnology, laboratory techniques, and quality assurance processes, often supported by a relevant degree in life sciences or biotechnology. Familiarity with regulatory standards such as GMP or ISO, data analysis software, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, effective communication, and the ability to work independently are important soft skills in remote settings. These competencies ensure accurate quality assessments, regulatory compliance, and effective collaboration with distributed teams.
What are the most common challenges faced by remote quality control professionals in the biotech industry?
One of the main challenges faced by remote quality control biotech professionals is maintaining effective communication and collaboration with on-site laboratory teams and cross-functional departments. Since much of the data review, reporting, and troubleshooting are performed remotely, it can also be challenging to stay updated with real-time lab processes and quickly resolve discrepancies. To address these issues, many companies use digital collaboration tools, regular virtual meetings, and thorough documentation practices. Adapting to these remote workflows ensures that quality standards are consistently met even from a distance.
What are popular job titles related to Remote Quality Control Biotech jobs in Kentucky?
For Remote Quality Control Biotech jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Remote Quality Control Biotech jobs in Kentucky look for?
The top searched job categories for Remote Quality Control Biotech jobs in Kentucky are:
What cities in Kentucky are hiring for Remote Quality Control Biotech jobs?
Cities in Kentucky with the most Remote Quality Control Biotech job openings:
Full-time
Medical, PTO
This job post has expired 1 day ago. Applications are no longer accepted.
Job description
What You'll Do:
- Assist Auditors with Sponsor audits and regulatory authority inspections to facilitate the auditing & inspection process
- Manage and initiate regional testing for the annual update of the Business Continuity Plan
- Assist in tracking audit findings, deviations and CAPAS identified in a Quality Assurance Audit
- Quality control of Standard Operating Procedures (SOPs) ensuring consistency in formatting, spelling, etc.
- Manage the distribution process for company SOPs
- Recommend changes to current processes to provide more effective use of the LMS and take the lead to implement such changes
- Create/format document templates & trackers
- Maintain quality records per SOPs
- Work closely with Auditors to learn and enhance Quality Assurance responsibilities
- Assist with maintaining audit schedules and tracking of deliverables
- Assist QA Auditors with conducting Vendor Audits, Internal System Audits and Computerized Systems validation, gaining experience to begin completing these tasks independently
- Assist in coordination of all activities related to the QMS, including but not limited to co-administration, routine review of quality control documentation, and development and execution of system user acceptance testing documentation
- Assist with the creation of procedures and work instructions/job aids relating to the QMS ensuring consistency and quality of content
- Assist QMS Document owners/users with entry of data into QMS
- Assists management with timely and appropriate follow up of deviations and CAPAs in the QMS in accordance with internal policies/SOPs
- Assist with completion of RFIs related to Quality Management Systems
- International region-specific functions
What You'll Bring:
- Bachelor’s Degree or equivalent combination of education and experience
- 0-1 years of work experience
- Basic understanding of GxP Guidelines, namely ICH/GCP Guidelines and relevant country specific regulations
- Excellent verbal and written communication skills
About CTI
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
- Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
- Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
- Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.
Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
- We will never communicate with you via Microsoft Teams or text message
- We will never ask for your bank account information at any point during the recruitment process
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.