... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
Quick apply
... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
Forklift Loader and Unloader
$14.25 - $17.25/hr
... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
Forklift Loader and Unloader
$14.25 - $17.25/hr
... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
Manufacturing Food Production Operator
Granite City, IL · On-site
$17 - $19/hr
... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
Quick apply
Manufacturing Food Production Operator
Granite City, IL · On-site
$17 - $19/hr
... and FDA regulated ingredients and products, Celta must restrict access to the warehouse and ... Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 ...
FDA form 1572, protocol signature page, delegation of authority logs, etc) and IRB submissions by collaborating with research nurses, clinical research coordinators, and investigators in the ...
FDA form 1572, protocol signature page, delegation of authority logs, etc) and IRB submissions by collaborating with research nurses, clinical research coordinators, and investigators in the ...
Regulatory Specialist II (Oncology)
Baltimore, MD · On-site
$41K - $72K/yr
Prepare and manage required regulatory documentation, including financial disclosure forms, delegation logs, FDA Form 1572, and others. * Maintain an organized regulatory binder (electronic or ...
Regulatory Specialist II (Oncology)
Baltimore, MD · On-site
$41K - $72K/yr
Prepare and manage required regulatory documentation, including financial disclosure forms, delegation logs, FDA Form 1572, and others. * Maintain an organized regulatory binder (electronic or ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
Maintain oversight of all trial-related medical decisions as outlined in FDA Form 1572 * Supervise and support delegated research staff, ensuring appropriate training and compliance * Ensure studies ...
Maintain oversight of all trial-related medical decisions as outlined in FDA Form 1572 * Supervise and support delegated research staff, ensuring appropriate training and compliance * Ensure studies ...
Clinical Research Associate-Regulatory
$22.83 - $34.51/hr
Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice ... Conflict Of Interest (COI)/Financial Disclosure; 1571/1572/IDE Documentation; Training ...
Clinical Research Associate-Regulatory
$22.83 - $34.51/hr
Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice ... Conflict Of Interest (COI)/Financial Disclosure; 1571/1572/IDE Documentation; Training ...
Clinical Trial Specialist
Johnson City, TN · On-site
Monitor regulatory documents (e.g., Form 1572, delegation logs) for accuracy and completeness ... Maintain awareness of and compliance with FDA, ICH-GCP, and institutional regulatory standards for ...
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Clinical Trial Specialist
Johnson City, TN · On-site
Monitor regulatory documents (e.g., Form 1572, delegation logs) for accuracy and completeness ... Maintain awareness of and compliance with FDA, ICH-GCP, and institutional regulatory standards for ...
Clinical Trial Specialist
Johnson City, TN · On-site
Monitor regulatory documents (e.g., Form 1572, delegation logs) for accuracy and completeness ... Maintain awareness of and compliance with FDA, ICH-GCP, and institutional regulatory standards for ...
Quick apply
Clinical Trial Specialist
Johnson City, TN · On-site
Monitor regulatory documents (e.g., Form 1572, delegation logs) for accuracy and completeness ... Maintain awareness of and compliance with FDA, ICH-GCP, and institutional regulatory standards for ...
Clinical Research - Regulatory Specialist
Anaheim, CA · On-site
$30 - $35/hr
Submission documents/approval, Protocol amendments with respective signature pages, Informed consent documents, FDA form 1572, Lab normal result documents, financial disclosure forms, Delegation of ...
Clinical Research - Regulatory Specialist
Anaheim, CA · On-site
$30 - $35/hr
Submission documents/approval, Protocol amendments with respective signature pages, Informed consent documents, FDA form 1572, Lab normal result documents, financial disclosure forms, Delegation of ...
As Principal Investigator and as signatory on FDA Form 1572, provides oversight to all staff who are directly involved in study execution. * Functions as the Principal Investigator or Sub ...
As Principal Investigator and as signatory on FDA Form 1572, provides oversight to all staff who are directly involved in study execution. * Functions as the Principal Investigator or Sub ...
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
Principal Investigator
Baltimore, MD · On-site
Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572 * Support inspections, audits, and regulatory interactions when required Team Leadership * Mentor and guide ...
Principal Investigator
Baltimore, MD · On-site
Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572 * Support inspections, audits, and regulatory interactions when required Team Leadership * Mentor and guide ...
Regulatory Coordinator
Hollywood, FL · On-site
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
Regulatory Coordinator
Hollywood, FL · On-site
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
Regulatory Coordinator
Hollywood, FL · On-site
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
Regulatory Coordinator
Hollywood, FL · On-site
... FDA form 1572 * o Lab normal result documents * o financial disclosure forms * o Delegation of authority logs * o Licenses * o Reports * o Logs (e.g., temperature logs, drug accountability logs ...
Research Nurse Coordinator RN - Cardiology - 10 hour shift 6:30am-5:00pm
Gainesville, GA · On-site
$64K - $80K/yr
Confirm that all regulatory documents are submitted to sponsor in a timely manner, e.g., 1572 ... Maintain strong working knowledge of Standard Operating Procedures (SOPs), FDA regulations, and ...
Research Nurse Coordinator RN - Cardiology - 10 hour shift 6:30am-5:00pm
Gainesville, GA · On-site
$64K - $80K/yr
Confirm that all regulatory documents are submitted to sponsor in a timely manner, e.g., 1572 ... Maintain strong working knowledge of Standard Operating Procedures (SOPs), FDA regulations, and ...
Principal Investigator
Baltimore, MD · On-site
$200K - $285K/yr
Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572 * Support inspections, audits, and regulatory interactions when required Team Leadership * Mentor and guide ...
Principal Investigator
Baltimore, MD · On-site
$200K - $285K/yr
Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572 * Support inspections, audits, and regulatory interactions when required Team Leadership * Mentor and guide ...
Clinical Research - Regulatory Specialist
Anaheim, CA · On-site
$30 - $35/hr
Submission documents/approval, Protocol amendments with respective signature pages, Informed consent documents, FDA form 1572, Lab normal result documents, financial disclosure forms, Delegation of ...
Clinical Research - Regulatory Specialist
Anaheim, CA · On-site
$30 - $35/hr
Submission documents/approval, Protocol amendments with respective signature pages, Informed consent documents, FDA form 1572, Lab normal result documents, financial disclosure forms, Delegation of ...
Research Nurse Coordinator RN - Cardiology - 10 hour shift 6:30am-5:00pm
Gainesville, GA · On-site
$64K - $80K/yr
Confirm that all regulatory documents are submitted to sponsor in a timely manner, e.g., 1572 ... Maintain strong working knowledge of Standard Operating Procedures (SOPs), FDA regulations, and ...
Research Nurse Coordinator RN - Cardiology - 10 hour shift 6:30am-5:00pm
Gainesville, GA · On-site
$64K - $80K/yr
Confirm that all regulatory documents are submitted to sponsor in a timely manner, e.g., 1572 ... Maintain strong working knowledge of Standard Operating Procedures (SOPs), FDA regulations, and ...
Fda 1572 information
What is the difference between Fda 1572 vs Clinical Research Coordinator?
| Aspect | Fda 1572 | Clinical Research Coordinator |
|---|---|---|
| Required credentials | Physicians or qualified investigators | Educational background in health/science, often with certifications |
| Work environment | Regulatory submissions, clinical trial oversight | Managing daily trial activities, patient interactions |
| Employer/industry usage | Pharmaceutical companies, regulatory agencies | Research institutions, hospitals, CROs |
Fda 1572 is a form completed by investigators to ensure compliance with FDA regulations, mainly used by physicians involved in clinical trials. Clinical Research Coordinators manage trial logistics and patient coordination. While both roles are integral to clinical research, Fda 1572 focuses on investigator compliance, whereas Coordinators handle trial operations.
$17 - $19/hr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 17 days ago
Job description
Benefits:
About Celta Industries
Celta Industries is a dynamic and growing manufacturer and distributor of food-grade oils, specialty ingredients, and chemical products servicing a wide array of industrial sectors. With a firm commitment to product safety, regulatory compliance, and operational excellence, we strive to be an industry leader in quality, integrity, and innovation.
Key Responsibilities
Report to work at Granite City, IL M-F 7:00am 3:30pm
Operate Machinery and Equipment
- Set up, operate, and monitor machines involved in food production.
- Adjust machine settings for speed, temperature, and ingredient mix levels.
- Operate a forklift to move raw materials, packaging, and finished products.
Production Monitoring
- Observe production lines to ensure product quality and consistency.
Quality Control
- Perform regular quality checks (e.g., weight, appearance).
- Ensure compliance with food safety and hygiene standards (e.g., HACCP, GMP).
Ingredient Handling
- Measure and mix ingredients according to recipes or batch records.
- Load raw materials into production equipment.
Cleaning and Sanitation
- Clean equipment and work areas in accordance with sanitation and safety standards.
- Follow scheduled cleaning protocols to avoid contamination.
Packaging and Labeling
- Operate packaging machines and label products correctly.
Recordkeeping
- Maintain accurate production and quality control records.
- Complete logs and reports for traceability and regulatory compliance.
Team Collaboration
- Communicate with supervisors and team members to coordinate workflow.
- Assist in training new operators or temporary staff.
Required Qualifications
- 18 years of age
- High school degree, or equivalent
- Must be able to pass a background check
- Must be able to pass a drug test to operate heavy machinery
- Must be able to pass a respirator fitness test and maintain that fitness
- Must be able to wear appropriate personal protective equipment and work in environments where food-grade and chemical products are handled
- Maintain valid drivers license
- Capable of being trained to operate equipment, like a forklift, and follow procedures accurately and safely in a timely manner
- Capable of being trained to complete required paperwork associated with job functions
- Capable of lifting and carrying at least 50 lbs, repeatedly
- Capable of walking up and down stairs and ladders unassisted
- Cannot be legally blind
- Prior experience a plus
What We Offer
- Group Health Insurance Options Celta pays at least 90% for Employees and at least 80% for Employees and Family (depending on chosen plan)
- Group Vision & Dental Insurance Celta pays 50% for Employees and Family
- Voluntary Life, Accident, and Critical Illness available
- Accrue up to 10 days of Vacation Time Off per year
- Accrue up to 40 hours of Sick Leave each year
- 8 Paid Holidays
- 401K Profit Share
- Training and development opportunities
- A mission-driven, safety-first, and team-oriented culture
Notice for Food Operator Applicants
Due to work with Hazardous Materials and FDA regulated ingredients and products, Celta must restrict access to the warehouse and products to reduce risk of terrorism, fraud and intentional adulteration of food-related products. Criminal Background checks will be performed on all new hires to check applicants criminal history, mental health, immigration status, and presence on watchlists before authorizing them to work with Hazmat and food production. This may include prior work history, criminal checks of county, metro, state and federal records going back up to 7 years and FACIS level 1M screening. Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 1572.103., are legally authorized to work in the U.S., and do not appear on any global sanctions watchlists. To operate heavy machinery safely, applicants must be able to pass a drug test.
- Dental insurance
- Health insurance
- Opportunity for advancement
- Paid time off
- Profit sharing
- Vision insurance
About Celta Industries
Celta Industries is a dynamic and growing manufacturer and distributor of food-grade oils, specialty ingredients, and chemical products servicing a wide array of industrial sectors. With a firm commitment to product safety, regulatory compliance, and operational excellence, we strive to be an industry leader in quality, integrity, and innovation.
Key Responsibilities
Report to work at Granite City, IL M-F 7:00am 3:30pm
Operate Machinery and Equipment
- Set up, operate, and monitor machines involved in food production.
- Adjust machine settings for speed, temperature, and ingredient mix levels.
- Operate a forklift to move raw materials, packaging, and finished products.
Production Monitoring
- Observe production lines to ensure product quality and consistency.
Quality Control
- Perform regular quality checks (e.g., weight, appearance).
- Ensure compliance with food safety and hygiene standards (e.g., HACCP, GMP).
Ingredient Handling
- Measure and mix ingredients according to recipes or batch records.
- Load raw materials into production equipment.
Cleaning and Sanitation
- Clean equipment and work areas in accordance with sanitation and safety standards.
- Follow scheduled cleaning protocols to avoid contamination.
Packaging and Labeling
- Operate packaging machines and label products correctly.
Recordkeeping
- Maintain accurate production and quality control records.
- Complete logs and reports for traceability and regulatory compliance.
Team Collaboration
- Communicate with supervisors and team members to coordinate workflow.
- Assist in training new operators or temporary staff.
Required Qualifications
- 18 years of age
- High school degree, or equivalent
- Must be able to pass a background check
- Must be able to pass a drug test to operate heavy machinery
- Must be able to pass a respirator fitness test and maintain that fitness
- Must be able to wear appropriate personal protective equipment and work in environments where food-grade and chemical products are handled
- Maintain valid drivers license
- Capable of being trained to operate equipment, like a forklift, and follow procedures accurately and safely in a timely manner
- Capable of being trained to complete required paperwork associated with job functions
- Capable of lifting and carrying at least 50 lbs, repeatedly
- Capable of walking up and down stairs and ladders unassisted
- Cannot be legally blind
- Prior experience a plus
What We Offer
- Group Health Insurance Options Celta pays at least 90% for Employees and at least 80% for Employees and Family (depending on chosen plan)
- Group Vision & Dental Insurance Celta pays 50% for Employees and Family
- Voluntary Life, Accident, and Critical Illness available
- Accrue up to 10 days of Vacation Time Off per year
- Accrue up to 40 hours of Sick Leave each year
- 8 Paid Holidays
- 401K Profit Share
- Training and development opportunities
- A mission-driven, safety-first, and team-oriented culture
Notice for Food Operator Applicants
Due to work with Hazardous Materials and FDA regulated ingredients and products, Celta must restrict access to the warehouse and products to reduce risk of terrorism, fraud and intentional adulteration of food-related products. Criminal Background checks will be performed on all new hires to check applicants criminal history, mental health, immigration status, and presence on watchlists before authorizing them to work with Hazmat and food production. This may include prior work history, criminal checks of county, metro, state and federal records going back up to 7 years and FACIS level 1M screening. Celta employees must not have any disqualifying criminal convictions specified in 49 CFR, Part 1572 1572.103., are legally authorized to work in the U.S., and do not appear on any global sanctions watchlists. To operate heavy machinery safely, applicants must be able to pass a drug test.