Consulting (Project Delivery, SOW), etc. Our Staff Members Our in-house team offers a broad range ... Our Recruiting Management and staff members at ICONMA understand that our greatest assets are our ...
Consulting (Project Delivery, SOW), etc. Our Staff Members Our in-house team offers a broad range ... Our Recruiting Management and staff members at ICONMA understand that our greatest assets are our ...
... ies), consulting firm, CRO or FDA. * Experience leading teams of technical professionals. We ... manager. All applications will be treated on their own merit and candidates will not be at any ...
... ies), consulting firm, CRO or FDA. * Experience leading teams of technical professionals. We ... manager. All applications will be treated on their own merit and candidates will not be at any ...
Technical Sales Manager - U.S. Meat Processing (Maurer-Atmos)
Elk Grove Village, IL · On-site +1
$95K - $120K/yr
Consultative Strategy: Perform on-site process analyses to help clients maximize yield, capacity ... Solid understanding of USDA/FDA requirements and HACCP principles. * The Road Warrior Spirit:
Technical Sales Manager - U.S. Meat Processing (Maurer-Atmos)
Elk Grove Village, IL · On-site +1
$95K - $120K/yr
Consultative Strategy: Perform on-site process analyses to help clients maximize yield, capacity ... Solid understanding of USDA/FDA requirements and HACCP principles. * The Road Warrior Spirit:
TMS Technician
Wheaton, IL · On-site
$38K - $45K/yr
... manager. Primary responsibilities are, but not limited to: · Providing educational consultations ... FDA-Approved, non-invasive, non-systemic treatment for severe depression, OCD, and more. At our ...
Quick apply
TMS Technician
Wheaton, IL · On-site
$38K - $45K/yr
... manager. Primary responsibilities are, but not limited to: · Providing educational consultations ... FDA-Approved, non-invasive, non-systemic treatment for severe depression, OCD, and more. At our ...
Sr. Project Manager
Lake Forest, IL · On-site
$55 - $57/hr
... R&D, and FDA regulated products. * Proven leadership skills, results oriented, highly ... Consultants Eligible Benefits Upon Waiting Period: * Medical and Prescription Drug Plans * Dental ...
Sr. Project Manager
Lake Forest, IL · On-site
$55 - $57/hr
... R&D, and FDA regulated products. * Proven leadership skills, results oriented, highly ... Consultants Eligible Benefits Upon Waiting Period: * Medical and Prescription Drug Plans * Dental ...
Lab Analyst
Aurora, IL · On-site
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...
Lab Analyst
Aurora, IL · On-site
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Communicate delays or field issues to the Traffic Manager/Supervisor * Maintain a professional ...
Quick apply
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Communicate delays or field issues to the Traffic Manager/Supervisor * Maintain a professional ...
Lab Analyst
Aurora, IL · On-site
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...
Quick apply
Lab Analyst
Aurora, IL · On-site
... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...
Management of projects within established scope, schedule, andbudget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Management of projects within established scope, schedule, andbudget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Quick apply
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Sales Account Executive
Chicago, IL · On-site
$80 - $90K/hr
Drive Consultative Sales for MedTech and Life Sciences clients, including: * Digital, embedded, and ... FDA, ISO, MDR, IVDR, Remediation) * Documentation and quality management services * Identify ...
Quick apply
Sales Account Executive
Chicago, IL · On-site
$80 - $90K/hr
Drive Consultative Sales for MedTech and Life Sciences clients, including: * Digital, embedded, and ... FDA, ISO, MDR, IVDR, Remediation) * Documentation and quality management services * Identify ...
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Management of projects within established scope, schedule, and budget while meeting and exceeding ... Have familiarity with GMP, FDA, OSHA, ISO, and environmental requirements * Willingness to travel ...
Quality Engineer - Medical Device Manufacturing
Vernon Hills, IL · On-site
$80K - $90K/yr
Manage quality test methods and validate standards used in production * Keep production compliant ... FDA, GMP, and ISO medical device requirements * Lead root cause investigations for SCARs, non ...
Quality Engineer - Medical Device Manufacturing
Vernon Hills, IL · On-site
$80K - $90K/yr
Manage quality test methods and validate standards used in production * Keep production compliant ... FDA, GMP, and ISO medical device requirements * Lead root cause investigations for SCARs, non ...
Territory Manager - Chicago, IL
Chicago, IL · On-site +1
Food and Drug Administration (FDA), including ZOLYMBUS™, IYUZEH™, Zioptan ® , Cosopt ® ... Build strong, consultative relationships with optometrists, technicians, office managers, and ...
Territory Manager - Chicago, IL
Chicago, IL · On-site +1
Food and Drug Administration (FDA), including ZOLYMBUS™, IYUZEH™, Zioptan ® , Cosopt ® ... Build strong, consultative relationships with optometrists, technicians, office managers, and ...
S. Food and Drug Administration (FDA), including ZOLYMBUS, IYUZEH, Zioptan, Cosopt, Cosopt PF ... Build strong, consultative relationships with optometrists, technicians, office managers, and ...
S. Food and Drug Administration (FDA), including ZOLYMBUS, IYUZEH, Zioptan, Cosopt, Cosopt PF ... Build strong, consultative relationships with optometrists, technicians, office managers, and ...
Inside Sales Representative
Wheeling, IL · On-site
The ideal candidate thrives in a fast-paced, growth-oriented environment, understands consultative ... Familiarity with GMP, FDA, US Pharmacopeia ICH guidelines, or quality systems * CRM experience ...
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Inside Sales Representative
Wheeling, IL · On-site
The ideal candidate thrives in a fast-paced, growth-oriented environment, understands consultative ... Familiarity with GMP, FDA, US Pharmacopeia ICH guidelines, or quality systems * CRM experience ...
Technical Leader
$130K - $160K/yr
Strong knowledge of regulatory requirements (FDA, ISO, etc.) * Proficiency in CAD software, Solid ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...
Technical Leader
$130K - $160K/yr
Strong knowledge of regulatory requirements (FDA, ISO, etc.) * Proficiency in CAD software, Solid ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...
Technical Leader
Chicago, IL · On-site
$130K - $160K/yr
Strong knowledge of regulatory requirements (FDA, ISO, etc.) * Proficiency in CAD software, Solid ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...
Technical Leader
Chicago, IL · On-site
$130K - $160K/yr
Strong knowledge of regulatory requirements (FDA, ISO, etc.) * Proficiency in CAD software, Solid ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...
Material Handler
Itasca, IL · On-site
$18 - $23/hr
Support all Company initiatives as identified by management and in support of Quality Management ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...
Quick apply
Material Handler
Itasca, IL · On-site
$18 - $23/hr
Support all Company initiatives as identified by management and in support of Quality Management ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...
Manager Fda Consulting information
What does a manager in FDA consulting do?
How does a manager in FDA consulting typically collaborate with cross-functional teams to ensure regulatory compliance for clients?
What are the key skills and qualifications needed to thrive as a manager in FDA consulting, and why are they important?
What is the difference between Manager Fda Consulting vs Regulatory Affairs Specialist?
| Aspect | Manager Fda Consulting | Regulatory Affairs Specialist |
|---|---|---|
| Credentials | Typically requires a bachelor's or master's in life sciences, with experience in FDA regulations | Usually holds a bachelor's degree in life sciences or related field, with certification preferred |
| Work Environment | Consulting firms, client sites, or remote; project-based work | In-house or pharmaceutical/medical device companies; regulatory departments |
| Industry Usage | Commonly employed in consulting firms advising multiple clients | Primarily employed within companies managing regulatory submissions |
While both roles require knowledge of FDA regulations, a Manager Fda Consulting typically leads consulting projects and advises clients, whereas a Regulatory Affairs Specialist manages regulatory submissions within a company. The roles differ mainly in scope, environment, and responsibilities, but share core regulatory knowledge.
What job categories do people searching Manager Fda Consulting jobs in Park Ridge, IL look for?
The top searched job categories for Manager Fda Consulting jobs in Park Ridge, IL are:
What cities near Park Ridge, IL are hiring for Manager Fda Consulting jobs?
Cities near Park Ridge, IL with the most Manager Fda Consulting job openings:

Job description
Our Unique Capabilities
We have a unique ability to provide a full spectrum of Staffing Services and Solutions including: Staff Augmentation (Contract, Contract-to-Hire, Direct Hire); Bulk Buy Staff Augmentation; Offshore Staff Augmentation; Payroll Services; Consulting (Project Delivery, SOW), etc.
Our Staff Members
Our in-house team offers a broad range of Information Technology, Engineering, Accounting/ Finance, Scientific/Clinical, Professional, Mortgage, Administrative/Office, Call Center, Human Resources, and Marketing/Creative expertise.
Our Recruiting
Management and staff members at ICONMA understand that our greatest assets are our highly skilled and professional consultants. Because of this, we have created a work environment which fosters career development, stability and personal growth. The result for our customers' is a knowledgeable and stable consulting staff whom they can depend on to operate more productively and to improve profitability, top-line growth, customer service, and cost management.
Specialist/Technical Writer
Location: Lake Forest, IL
Duration: 4 months
Description:
Primary Function:
Reporting to the Remediation Manager for Quality Systems, the Documentation Specialist will be responsible for reviewing and writing pharmaceutical/medical documentation (e.g. batch records, specifications, procedures, reports, SOPs, etc.) to provide clear and correct instructions for site processes and procedures. Will be responsible for the review and assessment of site documentation to ensure synchronization of content and format with corporate documentation. Will be responsible for identification and recommendation of best industry practices for documentation format. Will participate in transition from paper-based to electronic record keeping strategies. Will identify and provide recommended corrective actions for site documentation activities.
Major Duties and Responsibilities:
Review, edit or develop documentation (e.g. batch records, specifications, procedures, reports, SOPs, etc.) connected to specific project timelines. Assist in strategy development to transition to electronic documentation platform. Review and assess site documents to ensure compliance with corporate documents. Make recommendations for documentation content and format to support employee understanding of batch records, specification, procedures, and SOPs, etc. Support transition to electronic documentation platform. Identify commonalities and linkages in different documents to optimize common remediation activities. Active member of the remediation team to rectify the documentation gaps identified in the gap assessments working within a cross functional team which may include R&D, Quality, Manufacturing, Engineering, Regulatory Affairs, and Documentation Control. Assures compliance to all regulatory standards Travel to other Company sites as needed.
Skills/Experience/Education:
A Bachelor's Degree is required, preferably with an educational background in science, engineering, manufacturing, or business in order to interact effectively with resources experienced in Manufacturing, Engineering, and Quality Assurance.
Experience in technical writing and/or procedure development, preferably in FDA regulated environment. Excellent communication skills and attention to detail Proficient with Microsoft Office (Excel, Word, Powerpoint). Visio preferred.
Capable of organizing data from multiple sources, extracting key information and writing reports and summaries Demonstrated ability to write logically and consistently Strong critical thinking and problem solving skills Resourceful and innovative approach Ability to work cross-functionally
A Bachelor's Degree is required, preferably with an educational background in science, engineering, manufacturing, or business in order to interact effectively with resources experienced in Manufacturing, Engineering, and Quality Assurance
Experience in technical writing and/or procedure development, preferably in FDA regulated environment. Excellent communication skills and attention to detail Proficient with Microsoft Office (Excel, Word, Powerpoint). Visio preferred.
About ICONMA
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ICONMA is an established and stable organization building lasting relationships with clients and consultants. We are unique in our ability to provide a full spectrum of Staffing Services and Solutions including: Staff Augmentation (Contract, Contract-to-Hire, Direct Hire), Bulk Buy Staff Augmentation, Offshore Staff Augmentation, Payroll Services and Consulting (Project Delivery, SOW). At ICONMA, our goal is to become a one-stop destination for our customers' staffing and outsourcing needs. Our vision is to be a preeminent provider of innovative business solutions, leveraging key technologies to improve our customers' competitiveness, growth, and profitability. ICONMA focuses on a culture that fosters collaboration and team work. We recognize that employees are the foundation of any company, and we encourage our employees to be leaders while providing continuous training and growth opportunities. ICONMA encourages hard work, determination and dedication in a professional environment. ICONMA promotes a healthy work-life balance, and understands this is a key component to our employee's and company's success.
Industry
Recruiting and staffing services
Company size
1,001 - 5,000 Employees
Headquarters location
Troy, MI, US
Year founded
2000