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Biotech Assistant Jobs in Powder Springs, GA (NOW HIRING)

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Stay current on changes in regulatory requirements and assist in assessing the impact on company ...

... biotech or medical device experience. * Minimum of 2 years reimbursement experience required. * Ability to communicate cross-functionally within the region to share results, assist training and ...

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and ... that will assist our clients in developing and marketing life-changing therapies to positively ...

... Biotechnology, Bioinformatics, or related field required. 5. Must exhibit a positive attitude and ... Write training programs and guides in order to assist all healthcare staff in correct machinery ...

New

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... They will assist in goal setting, training, supporting DS educational efforts, and overall ...

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... They will assist in goal setting, training, supporting DS educational efforts, and overall ...

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... They will assist in goal setting, training, supporting DS educational efforts, and overall ...

BioMed Engineer I

Riverdale, GA · On-site

$22.75 - $30.25/hr

... Biotechnology, Bioinformatics, or related field required. 5. Must exhibit a positive attitude and ... Write training programs and guides in order to assist all healthcare staff in correct machinery ...

New

BioMed Engineer I

Riverdale, GA · On-site

$22.75 - $30.25/hr

... Biotechnology, Bioinformatics, or related field required. 5. Must exhibit a positive attitude and ... Write training programs and guides in order to assist all healthcare staff in correct machinery ...

New

... * Assist with estimating permissions-related costs and communicating requirements to internal ... Bachelor's degree in life sciences, pharmacy, biotechnology, or related field preferred.

... * Assist with estimating permissions-related costs and communicating requirements to internal ... Bachelor's degree in life sciences, pharmacy, biotechnology, or related field preferred.

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... * Assist in the preparation for regulatory inspections and third-party audits, serving as a key ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... * Assist in the preparation for regulatory inspections and third-party audits, serving as a key ...

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply ... Ensure all company activities and operations comply with applicable laws and regulations. * Assist ...

Showing results 41-60

Biotech Assistant information

What is a biotech assistant?

A Biotech Assistant supports scientists and researchers in biotechnology labs by conducting experiments, preparing materials, and maintaining equipment. They assist in data collection, documentation, and laboratory safety procedures. Their role helps advance research in areas like pharmaceuticals, agriculture, and genetics. Strong attention to detail and knowledge of lab techniques are essential for success in this position.

What does a biotech assistant do?

A typical day for a Biotech Assistant involves preparing and maintaining laboratory equipment, assisting with experiments, recording and analyzing data, and ensuring all safety procedures are followed. You may also be responsible for managing laboratory supplies, disposing of hazardous materials correctly, and collaborating closely with research scientists and other lab staff. The work is detail-oriented and often requires managing multiple tasks simultaneously. Teamwork and effective communication are important as you often support ongoing projects and help troubleshoot minor issues that arise during experiments.

What skills and qualifications are needed to thrive as a biotech assistant?

To thrive as a Biotech Assistant, you should have a background in biology or a related science, strong laboratory skills, and meticulous attention to detail, often supported by an associate's or bachelor's degree. Familiarity with laboratory equipment, safety protocols, and data management systems such as LIMS is typically required. Excellent organization, communication, and teamwork skills help you excel when supporting scientists and handling multiple tasks. These abilities are crucial for ensuring accurate experimental results, maintaining lab safety, and contributing to research success.

What are the most commonly searched types of Biotech jobs in Powder Springs, GA?

The most popular types of Biotech jobs in Powder Springs, GA are:

What job categories do people searching Biotech Assistant jobs in Powder Springs, GA look for?

The top searched job categories for Biotech Assistant jobs in Powder Springs, GA are:

Regulatory Affairs Manager (Atlanta)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 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.