1

Master In Biotechnology Jobs in Atlanta, GA (NOW HIRING)

... national biotech organization focused on pushing the limits of innovation and supply in global ... Master's degree preferred. Professional Experience: * 5-7 years of regulatory affairs experience ...

... national biotech organization focused on pushing the limits of innovation and supply in global ... Master's degree or certifications (e.g., CPIM, CSCP). * Knowledge of FDA, GMP, and ISO regulations.

... national biotech organization, focused on pushing the limits of innovation and supply in global ... Requirements Master's degree in Finance, Accounting Minimum of 10 years of experience in finance ...

... national biotech organization, focused on pushing the limits of innovation and supply in global ... Requirements • Master's degree in Finance, Accounting • Minimum of 10 years of experience in ...

... national biotech organization focused on pushing the limits of innovation and supply in global ... Master's degree or certifications (e.g., CPIM, CSCP). * Knowledge of FDA, GMP, and ISO regulations.

... national biotech organization focused on pushing the limits of innovation and supply in global ... Master's degree or certifications (e.g., CPIM, CSCP). * Knowledge of FDA, GMP, and ISO regulations.

About the role CorDx, a leader in the biotechnology industry, is seeking an experienced and ... Digital Marketing * Requirements * Bachelor's or master's degree in Marketing, Business ...

About the role CorDx, a leader in the biotechnology industry, is seeking an experienced and ... Digital Marketing * Requirements * Bachelor's or master's degree in Marketing, Business ...

About the role CorDx, a leader in the biotechnology industry, is seeking an experienced and ... Digital Marketing Requirements * Bachelor's or master's degree in Marketing, Business ...

... Master's degree in Engineering, Operations, Supply Chain/Logistics, or a related field. - Industry experience in: retail, F&B, military, manufacturing, automotive, biotech, electronics, energy ...

Showing results 41-60

Master In Biotechnology information

What is the difference between Master In Biotechnology vs Biotechnology Research Associate?

CriteriaMaster In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's or Master's degree in Biotechnology or related field
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, biotech companies, research organizations
Employer & Industry UsageAcademic, research, biotech industryBiotech companies, research labs, pharmaceutical firms
Common Search & ComparisonYesYes

The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.

What can I do with a master in biotechnology?

A master in biotechnology prepares individuals for roles such as research scientist, bioprocess engineer, quality control analyst, or regulatory affairs specialist. Graduates can work in pharmaceuticals, healthcare, agriculture, or environmental sectors, often utilizing laboratory skills, data analysis, and knowledge of biotech tools and regulations.

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

To thrive as a Master in Biotechnology, you need advanced knowledge in molecular biology, genetics, and laboratory techniques, typically supported by a master's degree in biotechnology or a related field. Familiarity with bioinformatics tools, PCR, and laboratory information management systems (LIMS) is essential, and certifications in laboratory safety can be advantageous. Strong problem-solving, critical thinking, and teamwork skills distinguish top professionals in this field. These competencies enable effective research, innovation, and collaboration in the rapidly evolving biotech industry.

What is a master in biotechnology?

A Master in Biotechnology is a graduate-level degree program focused on the advanced study of biological processes and the use of technology to manipulate living organisms for applications in medicine, agriculture, and industry. Students learn about molecular biology, genetics, bioinformatics, and laboratory techniques, as well as how to apply these skills to develop new products and solutions. This degree prepares graduates for careers in research, pharmaceuticals, healthcare, environmental management, and biotechnology companies, or for further study at the doctoral level.

What are typical career paths for a master in biotechnology, and how can they progress within the industry?

Graduates with a Master in Biotechnology can pursue diverse career paths, such as research scientist, quality control analyst, regulatory affairs specialist, or roles in product development and project management. Advancement often involves taking on leadership responsibilities, such as managing teams or projects, or specializing further in areas like bioinformatics or clinical research. Many professionals also transition into roles in biotech startups, pharmaceuticals, or government agencies, and may further their expertise through certifications or a doctoral degree. Networking, continuous skill development, and staying updated with industry trends are key to progressing within the biotechnology sector.
What are popular job titles related to Master In Biotechnology jobs in Atlanta, GA? For Master In Biotechnology jobs in Atlanta, GA, the most frequently searched job titles are:
What job categories do people searching Master In Biotechnology jobs in Atlanta, GA look for? The top searched job categories for Master In Biotechnology jobs in Atlanta, GA are:
Infographic showing various Master In Biotechnology job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, and 5% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Regulatory Affairs Manager (Atlanta)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 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.