Top 172 Senior product development Jobs in Covington Ga

Regulatory Affairs Manager
LGL Technologies —Covington, GA
- $145,000 - $160,000 a year
- Full-time
- Office
- 8 years
- Project management
- Relocation assistance
- Health insurance
Quick Apply
3d
Production Underwriter- Workers' Compensation
Stonetrust Commercial Insurance Company —Georgia
- $65,000 - $120,000 a year
- Full-time
- Remote
- Background check
- Mid-level
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
Quality Systems Supervisor
Golden State Foods —Conyers, GA
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- AD&D insurance
- Health insurance
Quick Apply
13d
Sr Process Engineer
INLINE PLASTICS CORP —McDonough, GA
- Evening shift
- 7 years
- Engineering
- English
- Flexible schedule
Quick Apply
Underwriting Technical Consultant
Builders Mutual —Georgia
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Organizational skills
- Paid holidays
- Paid time off
Quick Apply
13d
Manufacturing Packaging Engineer - Covington, GA
General Mills —Covington, GA
- $95,300 - $143,200 a year
- 12 hour shift
- 5 years
- Bachelor of Science
- Engineering
- Health insurance
Regulatory Affairs Manager
RuShaM IT Services LLC —Covington, GA
- $62,689.93 - $150,000.00 a year
- Full-time
- Hybrid work
- 3 years
- Master's degree
- Bachelor's degree
- Work from home
Quick Apply
3d
Cook
Benton House of Covington —Covington, GA
- Weekends as needed
- Organizational skills
- Communication skills
- Entry level
- Paid holidays
- Health insurance
Quick Apply
R&D Lab Manager
LioChem Inc. —Conyers, GA
- $115,000 - $140,000 a year
- Full-time
- Business development
- Bachelor's degree
- Organizational skills
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Senior Process Engineer
Quanex —Jackson, GA
- $68,500 - $100,000 a year
- Engineering
- Mid-level
- 2 years
- Employee stock purchase plan
- Paid holidays
3d
Business Development Manager (Southeast)
United States Cold Storage Inc —McDonough, GA
- $110,000 - $120,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Basic math
- Mid-level
- Commuter assistance
- AD&D insurance
Quick Apply
Senior Manager Regulatory Affairs
BD —Covington, GA
- Office
- 8 years
- Project management
Supervisor, Operations
ADMA Biologics —Conyers, GA
- Full-time
- Mid-level
- High school diploma or GED
- US work authorization
- Paid holidays
- Disability insurance
Senior Project Manager, R&D
BD —Covington, GA
- Spanish
- Engineering
- Office
Quality Manager
Pregis LLC —McDonough, GA
- Overtime
- Microsoft Outlook
- Computer literacy
- Engineering
Quick Apply
Sr. Plant Engineer
Takeda Pharmaceutical —Social Circle, GA
- $89,900 - $141,240 a year
- Weekends as needed
- Engineering
- English
- Office
Leasing and Compliance Manager
Fairway Management —Covington, GA
- Sales
- English
- Mid-level
- Fuel card
- Health insurance
Quick Apply
Sr Territory Manager - Southeast Region (Remote)
Parker Hannifin Corporation —Conyers, GA
- $106,490 - $177,635 a year
- Remote
- Up to 50% travel
- Travel
- Senior level
- Paid parental leave
- Paid holidays
Business Development Manager
Southern Metalcraft Inc —Social Circle, GA
- From $65,000 a year
- Full-time
- Hybrid work
- Background check
- Clean driving record
- Marketing
- Health insurance
- Dental insurance
Quick Apply
3d
Medication Technician
Benton House of Covington —Covington, GA
- Call employer
- 18 years or older
- CPR Certification
- BLS Certification
- Paid holidays
- Health insurance
Quick Apply

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senior product development jobs near covington ga

Regulatory Affairs Manager

LGL Technologies -
Covington, GA

Quick Apply

Job Details

Full-time
$145,000 - $160,000 a year
3 days ago

Benefits

Relocation assistance
Health insurance
Dental insurance
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Professional development assistance
Referral program
Retirement plan

Qualifications

Biology
FDA submissions
Team leadership
ISO standards
Project management
Bachelor's degree
Continuous improvement
Master of Science
Compliance documentation
Leading team collaboration initiatives
Chemistry
Regulatory submission editing and review
Biomedical regulatory compliance
Manufacturing company experience
Information management

Full Job Description

Job Responsibilities:

Develop and implement comprehensive regulatory strategies for new product development, product
life cycle management, and post-market surveillance activities.
Prepare, review, and submit regulatory documents, including 510(k)s, Dossiers, Technical Files, and other international submissions to global health authorities.
Act as the primary regulatory contact for assigned projects, communicating directly with regulatory agencies during submissions, reviews, and inspections.
Interpret and apply complex regulations, guidance documents, and industry standards to ensure product compliance throughout the development and commercialization process.
Lead and mentor junior regulatory affairs professionals, fostering a culture of compliance and continuous improvement.
Participate in internal and external audits, providing regulatory expertise and support.
Assess the regulatory impact of product changes, manufacturing changes, and quality system changes.
Collaborate effectively with R&D, Quality, Clinical, Marketing, and other relevant departments to achieve regulatory objectives.
Monitor and disseminate information regarding new or changing regulatory requirements and industry trends relevant to the company's product portfolio.

Job Qualifications:

Bachelor's degree in a scientific or technical discipline (e.g., Biomedical Engineering, Chemistry, Biology) required. Advanced degree (MS, PhD) preferred.
Minimum of 8-10 years of experience in Regulatory Affairs within the medical device industry, with at least 3-5 years in a leadership or senior role.
Demonstrated expertise in preparing and submitting various regulatory applications (e.g., 510(k), PMA, CE Mark, International registrations).
Strong knowledge of FDA regulations (21 CFR Parts 800s), ISO 13485, Medical Device Regulation (EU MDR), and other relevant international regulatory requirements.
Excellent written and verbal communication skills, with the ability to effectively communicate complex regulatory information to diverse audiences.
Proven ability to lead projects, manage multiple priorities, and work effectively in a fast-paced environment.
RAC (Regulatory Affairs Certification) preferred.
Proficiency in regulatory information management systems and tools.

Thanks,
HR Team | Lgl Technologies

Pay: $145,000.00 - $160,000.00 per year

Benefits:

401(k) matching
Dental insurance
Employee assistance program
Health insurance
Paid time off
Parental leave
Professional development assistance
Referral program
Relocation assistance
Retirement plan
Vision insurance

Education:

Bachelor's (Required)

Experience:

Regulatory Affairs Manager: 8 years (Preferred)
Medical device industry: 8 years (Required)
Leadership or Senior role: 3 years (Required)
Regulations (21 CFR Parts 800s), ISO 13485, (EU MDR): 3 years (Required)

Ability to Relocate:

Covington, GA 30014: Relocate with an employer provided relocation package (Required)

Work Location: In person

Quick Apply

Refine Your Search

senior product development jobs in covington ga

Regulatory Affairs Manager

Production Underwriter- Workers' Compensation

Quality Systems Supervisor

Sr Process Engineer

Underwriting Technical Consultant

Manufacturing Packaging Engineer - Covington, GA

Regulatory Affairs Manager

Cook

R&D Lab Manager

Senior Process Engineer

Business Development Manager (Southeast)

Senior Manager Regulatory Affairs

Supervisor, Operations

Senior Project Manager, R&D

Quality Manager

Sr. Plant Engineer

Leasing and Compliance Manager

Sr Territory Manager - Southeast Region (Remote)

Business Development Manager

Medication Technician

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