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Remote Quality Control Biotech Jobs in Georgia (NOW HIRING)

ESource Corp

Instructional designer-contractor

Suwanee, GA · Remote

$60K - $81K/yr

... biotech, medical device, and health system brands. Their Decision Engine integrates over 7.8 ... Manage timelines and version control to ensure on-time delivery and alignment with the broader ...

ESource Corp

Instructional designer-contractor

Suwanee, GA · On-site +1

$60K - $81K/yr

... biotech, medical device, and health system brands. Their Decision Engine integrates over 7.8 ... Manage timelines and version control to ensure on-time delivery and alignment with the broader ...

Beacon Talent

Mortgage Closing Specialist

Atlanta, GA · Remote

$95K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

This is a full-time remote role. Key Responsibilities * Own and manage the closing and post-closing ... Develop and implement standard operating procedures (SOPs), SLAs, QC frameworks, and checklists

micro1 AI

AI Training Specialist - Chemistry

Augusta, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

micro1 AI

AI Training Specialist - Chemistry

Atlanta, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

micro1 AI

AI Training Specialist - Chemistry

Savannah, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

micro1 AI

AI Training Specialist - Chemistry

Macon, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

micro1 AI

AI Training Specialist - Chemistry

Athens, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

micro1 AI

AI Training Specialist - Chemistry

Columbus, GA · Remote

$70 - $90/hr

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... quality control, or process optimization. * Design and interpret complex laboratory experiments ...

aldridgepite

Operations Specialist

Atlanta, GA · Remote

... remote and the hours are 11:00AM-8:00PM EST. Specific Duties, Activities and Responsibilities * Run SCRA/BK Checks * View and confirm SCRA/BK Checks via automation * Perform Quality Control of all ...

Switch

Mission Control Supervisor

Atlanta, GA · On-site +1

You are accountable for team performance during your shift, including quality, response times, and ... Flexibility & Remote Opportunities - Whether in-office, hybrid, or fully remote, we offer the ...

Harris

$55K - $65K/yr

Ability to manage priorities, meet deadlines, and work independently in a remote team environment ... Experience with source control concepts or tools. * Experience with API testing, integration ...

Switch, Inc.

Mission Control Supervisor

Atlanta, GA · On-site +1

You are accountable for team performance during your shift, including quality, response times, and ... Flexibility & Remote Opportunities Whether in-office, hybrid, or fully remote, we offer the ...

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All JobsQuality Control Biotech JobsRemote Quality Control Biotech JobsRemote Quality Control Biotech Jobs in Georgia

Remote Quality Control Biotech information

What skills and qualifications are needed for a remote quality control biotech?

To thrive as a Remote Quality Control Biotech, you generally need a solid background in biology or biotechnology, laboratory techniques, and quality assurance processes, often supported by a relevant degree in life sciences or biotechnology. Familiarity with regulatory standards such as GMP or ISO, data analysis software, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, effective communication, and the ability to work independently are important soft skills in remote settings. These competencies ensure accurate quality assessments, regulatory compliance, and effective collaboration with distributed teams.

What are the most common challenges faced by remote quality control professionals in the biotech industry?

One of the main challenges faced by remote quality control biotech professionals is maintaining effective communication and collaboration with on-site laboratory teams and cross-functional departments. Since much of the data review, reporting, and troubleshooting are performed remotely, it can also be challenging to stay updated with real-time lab processes and quickly resolve discrepancies. To address these issues, many companies use digital collaboration tools, regular virtual meetings, and thorough documentation practices. Adapting to these remote workflows ensures that quality standards are consistently met even from a distance.

What is a remote quality control biotech?

A Remote Quality Control Biotech job involves ensuring the quality, safety, and compliance of biotechnological products and processes while working remotely. Responsibilities may include reviewing data, conducting virtual audits, ensuring regulatory compliance, and collaborating with teams to maintain product integrity. Professionals in this role use digital tools to analyze laboratory results, monitor production processes, and document findings. Strong attention to detail, knowledge of industry regulations, and proficiency in data analysis are essential. This position is critical in maintaining high-quality biotech products while allowing flexibility through remote work.

What are popular job titles related to Remote Quality Control Biotech jobs in Georgia?

For Remote Quality Control Biotech jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Remote Quality Control Biotech jobs in Georgia look for?

The top searched job categories for Remote Quality Control Biotech jobs in Georgia are:

What cities in Georgia are hiring for Remote Quality Control Biotech jobs?

Cities in Georgia with the most Remote Quality Control Biotech job openings:

Remote Quality Control Biotech jobs near you

Senior Architect - Pharmaceutical & Life Sciences

SSOE, Inc.

Atlanta, GA • On-site, Remote

$95K - $121K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Job description

Overview
SSOE is seeking a Senior Architect with experience in pharmaceutical, biotechnology, and life sciences facilities to help design environments that advance scientific discovery, product quality, and patient safety. Working on complex cGMP manufacturing facilities, laboratories, and research spaces, you'll develop innovative, compliant solutions that support some of the industry's most critical operations. As a key technical leader, you'll collaborate within an integrated design-build team to drive projects from concept through delivery, applying your expertise in building codes, GMP regulations, and facility design. This role offers the opportunity to tackle challenging projects, mentor emerging professionals, expand your technical leadership, and make a lasting impact on the future of pharmaceutical and life sciences infrastructure.
AI and Innovation
At SSOE, we don't just talk about the future, we build it. As a leader in industry AI adoption, we empower our team to work smarter by providing responsible access to the industry leading AI Large Language Models, vibe-coding platforms, and securely integrating advanced tools into every role. From day one, you'll receive the training and support needed to leverage AI as a core tool for enhancing productivity, sparking creativity, and streamlining complex workflows.
Responsibilities
A Typical Day Might Include:
The following duties are typical of the position but are not all encompassing.
  • Lead and drive the architectural design and planning process for a portfolio of complex pharmaceutical and life sciences projects, including cGMP manufacturing suites, pilot plants, process development laboratories, quality control (QC) and quality assurance (QA) laboratories, research and development (R&D) laboratories, and associated warehouse and utility support facilities.
  • Provide technical leadership and day-to-day oversight to internal architectural project teams, ensuring the production of coordinated, high-quality construction documents that meet stringent client specifications, current Good Manufacturing Practice (cGMP) regulations, FDA guidance, and industry standards.
  • Guide the seamless integration of architectural design by collaborating closely with all of SSOE's engineering disciplines to ensure holistic coordination, constructability, and operational performance within a GMP environment.
  • Interpret and apply the relevant codes for all project phases, including in-depth interpretation and application of the International Building Code (IBC), International Existing Building Code (IEBC), International Fire Code (IFC), International Mechanical Code (IMC), NFPA 101 Life Safety Code, NFPA 45 (Fire Protection for Laboratories Using Chemicals), NFPA 30 (Flammable and Combustible Liquids Code), NFPA 400 (Hazardous Materials Code), and the full suite of accessibility codes and standards (ADA, ABA).
  • Apply knowledge of occupancy classifications (H, B, F-1), control area strategies per IBC, building height and area allowances, fire area separations, fire protection and suppression systems including gaseous and water mist systems for sensitive environments, egress strategies from classified spaces, fire-resistive construction, and accessibility requirements specific to laboratory and controlled production environments.
  • Interpret building code and GMP regulatory intent in ambiguous or specialized scenarios and provide authoritative guidance to internal teams, clients, and regulatory authorities.
  • Lead peer reviews, quality assurance/quality control checks, and constructability reviews, with a particular focus on GMP compliance, architectural finish detailing (seamless, cleanable, chemically resistant), cleanroom envelope integrity, and avoidance of ledges, cracks, and crevices that could harbor contamination.
  • Collaborate intensively with process engineers, validation specialists, commissioning/qualification (C&Q) teams, engineering, project management, and preconstruction teams in a design-build environment, contributing to early-phase planning, basis of design documentation, user requirement specifications (URS), design qualification (DQ), value engineering, target value delivery, and accelerated schedule alignment aligned with drug development milestones.
  • Develop and present design concepts, technical strategies, regulatory compliance approaches, and risk assessments to clients, including facility managers, quality assurance directors, and regulatory affairs teams; actively participate in client pursuit interviews and proposal development as part of ongoing business development efforts within the pharmaceutical and life sciences sector.
  • Mentor junior architects and technical staff within internal project teams, fostering deep understanding of GMP principles, cleanroom design, laboratory planning, regulatory frameworks, and the architectural detailing required for controlled environments.
  • Stay current with evolving GMP regulations, guidelines, and emerging trends such as continuous manufacturing, single-use technologies, modular cleanroom construction, and advanced therapy medicinal products (ATMPs); apply this knowledge to project delivery and firm standards.
  • Conduct periodic field observations and site visits to assess existing conditions within operating facilities, monitor construction progress, verify conformance with design intent and GMP requirements, and resolve design and compliance-related issues in real time; travel requirements are minimal and typically limited to regional project sites.
  • Lead the development and maintenance of architectural standards, master specifications, Revit templates, cleanroom detail libraries, material selection protocols, and documentation protocols to improve efficiency, consistency, GMP compliance, and quality across pharmaceutical and life sciences projects.

Qualifications
Qualifications You'll Need on Day One:
  • Bachelor's or Master's degree in Architecture from an accredited program.
  • Active Registered Architect (RA) license in good standing within the U.S., with ability to obtain reciprocity as needed (typically limited and not anticipated to be a frequent requirement).
  • 10+ years of architectural experience, with a strong and demonstrated focus on pharmaceutical, biotechnology, or life sciences facilities, including GMP manufacturing, laboratory, and/or pilot plant design.
  • Proven leadership in managing and guiding internal design teams through all project phases, from programming and concept design through construction administration and commissioning/qualification support, within a design-build delivery model.
  • Deep understanding of cGMP regulations, ISPE Baseline Guides, and their direct impact on architectural design, material selection, finish detailing, and spatial adjacencies for contamination control.
  • Expertise in interpreting and applying IBC, IFC, NFPA 45, NFPA 30, NFPA 400, NFPA 101, and ADA/ABA codes and standards within laboratory and pharmaceutical manufacturing occupancy types; thorough understanding of control area concept for hazardous materials management.
  • Working knowledge of cleanroom HVAC principles, including air changes per hour, HEPA filtration, pressure cascades, temperature/humidity control, and their spatial and architectural envelope implications.
  • Proficiency in Revit and BIM workflows is required; working knowledge of AutoCAD, Navisworks, Bluebeam, and other industry-standard tools is highly desirable.
  • Excellent communication, presentation, and client-facing skills, with the ability to clearly articulate complex technical, regulatory, and design concepts to diverse audiences including quality assurance, validation, operations, and facility management professionals.
  • A portfolio demonstrating thoughtful, code-compliant, and GMP-driven design solutions for pharmaceutical, biotech, or life sciences facilities.
  • Experience participating in activities such as, client interviews, proposal preparation, and relationship cultivation within the life sciences industry.
  • Salary Range: $120,000 - $160,000/year depending on location, education, depth of relevant experience, and any specialized licensure/certifications. Opportunity for ample rewards, leadership incentive components, and generous bonus opportunities.
  • Benefits: Includes comprehensive health, dental, and vision insurance, life insurance, 401K retirement savings plan (with company matching), opportunities for professional development and training (including support for relevant licensure & certifications), and generous PTO & paid holidays.

Preferred Qualifications:
  • Familiarity with commissioning, qualification, and validation (CQV) processes, including Design Qualification (DQ), Installation Qualification (IQ), and the architectural role in establishing the qualified facility envelope.
  • Knowledge of LEED or Green Globes certification application within laboratory and pharmaceutical environments; understanding of high-performance building envelope and energy reduction strategies for high-air-change facilities.
  • NCARB certification and ability to pursue architectural registration in multiple states.
  • Demonstrated success working within an integrated design-build project delivery environment on fast-track pharmaceutical projects.

Apply