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Biotechnology Project Manager Jobs in Decatur, GA

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... Strong organizational and project management skills with the ability to manage multiple projects ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$40/hr

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Exceptional organizational, project management, and leadership abilities. Preferred: * Master ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$40/hr

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... Exceptional organizational, project management, and leadership abilities. Preferred: * Master ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$40/hr

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... Exceptional organizational, project management, and leadership abilities. Preferred: * Master ...

Vero Biotech

Senior Accountant

Atlanta, GA

$71K - $89K/yr

Implement and maintain an accurate fixed asset management, tracking and reporting process/system ... Conduct special projects as assigned by the Corporate Controller. Qualifications Minimum of 2 years ...

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Biotechnology Project Manager information

See Decatur, GA salary details

$21

$45

$74

How much do biotechnology project manager jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for biotechnology project manager in Decatur, GA is $45.15, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $49.52 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What job categories do people searching Biotechnology Project Manager jobs in Decatur, GA look for?

The top searched job categories for Biotechnology Project Manager jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Biotechnology Project Manager jobs?

Cities near Decatur, GA with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Decatur, GA as of June 2026, with employment types broken down into 25% Full Time, and 75% Part Time. Highlights an 77% Physical, 2% Hybrid, and 21% Remote job distribution, with an average salary of $93,908 per year, or $45.1 per hour.

Regulatory Affairs Manager (Atlanta)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Job description

Who is CorDx？

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Job Type: Full time
Job Title: Regulatory Affairs Manager
Location: Onsite - Atlanta, GA

Position Summary:

The Regulatory Affairs Manager will support the preparation, review, and submission of regulatory documentation for medical device products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This position collaborates with cross-functional teams to provide regulatory input during product development and throughout the product lifecycle, helping to secure timely product approvals and regulatory clearances.

Key Responsibilities:

  • Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies.
  • Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards.
  • Provide regulatory support to product development teams by offering guidance on applicable regulations and documentation requirements.
  • Stay current on changes in regulatory requirements and assist in assessing the impact on company processes and products.
  • Perform regulatory assessments for product changes and propose appropriate regulatory pathways.
  • Maintain documentation and records of all regulatory submissions and correspondence.
  • Support the preparation for regulatory agency meetings, audits, and inspections.
  • Collaborate with internal departments such as R&D, Quality, and Operations to ensure regulatory deliverables are met in a timely manner.

Requirements

Education:

  • Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.
  • Master’s degree preferred.

Professional Experience:

  • 5–7 years of regulatory affairs experience within the medical device or IVD industry.
  • Working knowledge of 510(k) submissions and regulatory documentation processes.
  • Experience interacting with FDA and other regulatory agencies preferred.

Skills & Competencies:

  • Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements.
  • Strong organizational and project management skills with the ability to manage multiple projects and priorities.
  • Excellent communication, problem-solving, and attention to detail.
  • Ability to work collaboratively in cross-functional teams and manage document workflows.

Benefits

  • Highly competitive compensation package.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with generous company contributions.
  • Flexible paid time off (PTO) policy.
  • Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.