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Biotech Associate Jobs in Georgia (NOW HIRING)

Manus Bio

Mechanical Designer

Augusta, GA ยท On-site

... biotech and pharmaceutical manufacturing environments. Working under the direction of senior ... Associate's or Bachelor's degree in Mechanical Engineering Technology, Mechanical Design, or ...

Manus Bio

Mechanical Designer

Augusta, GA ยท On-site

... biotech and pharmaceutical manufacturing environments. Working under the direction of senior ... Associates or Bachelors degree in Mechanical Engineering Technology, Mechanical Design, or related ...

Gerresheimer

Assembly Process Technician

Peachtree City, GA

$16.25 - $20.50/hr

... biotech industry. www.gerresheimer.com Join Gerresheimer in Peachtree City, GA as a Mechanical ... Associate or Bachelor's in Engineering preferred * 2+ years in manufacturing or technical training;

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Biotech Associate information

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$9

$16

$28

How much do biotech associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotech associate in Georgia is $16.78, according to ZipRecruiter salary data. Most workers in this role earn between $12.60 and $17.45 per hour, depending on experience, location, and employer.

What is a biotech associate?

Biotech Associates are professionals who support scientific research, development, and production in biotechnology companies or laboratories. They typically assist in conducting experiments, analyzing data, preparing samples, and maintaining laboratory equipment. Their work helps develop new products or processes in areas like pharmaceuticals, agriculture, and environmental science. Biotech Associates often have a background in biology, chemistry, or related fields and work under the supervision of scientists or senior researchers.

What are the key skills and qualifications needed to thrive as a biotech associate?

To thrive as a Biotech Associate, you need a solid background in biology, chemistry, or a related field, usually supported by a bachelor's or master's degree. Familiarity with laboratory techniques, data analysis software, and compliance with regulatory standards like GLP or GMP is essential. Strong attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this position. These skills ensure accurate experimental results, regulatory compliance, and efficient collaboration in fast-paced research environments.

What are some typical challenges faced by biotech associates when working in a laboratory setting?

Biotech Associates often encounter challenges such as troubleshooting complex experiments, maintaining strict adherence to safety protocols, and managing multiple projects simultaneously. Working with sensitive biological materials requires attention to detail and the ability to quickly adapt to unexpected results or equipment malfunctions. Collaboration with scientists and cross-functional teams is frequent, so strong communication skills are essential to ensure experiments are aligned with broader research goals.

What is the difference between Biotech Associate vs Laboratory Technician?

AspectBiotech AssociateLaboratory Technician
Required CredentialsBachelor's degree in biology, biotech, or related field; some roles may require experienceAssociate's degree or relevant certification; less emphasis on advanced degrees
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsAcademic labs, industrial labs, healthcare facilities
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

The main difference between a Biotech Associate and a Laboratory Technician lies in their educational requirements and work scope. Biotech Associates typically hold a bachelor's degree and engage in research and development activities within biotech companies or research institutions. Laboratory Technicians often have an associate's degree and focus on routine lab tasks, testing, and sample processing. Both roles are essential in laboratory settings but differ in responsibilities and qualifications.

What are the most commonly searched types of Biotech jobs in Georgia?

The most popular types of Biotech jobs in Georgia are:

What are popular job titles related to Biotech Associate jobs in Georgia?

For Biotech Associate jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Biotech Associate jobs in Georgia look for?

The top searched job categories for Biotech Associate jobs in Georgia are:

What cities in Georgia are hiring for Biotech Associate jobs?

Cities in Georgia with the most Biotech Associate job openings:

Biotech Associate jobs near you
Infographic showing various Biotech Associate job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $34,896 per year, or $16.8 per hour.

Mechanical Designer

Manus Bio

Augusta, GA โ€ข On-site

Full-time

Re-posted 21 days ago

Job description

Position Summary
Manus works across industries and value chains to accelerate the transition to BioAlternatives ๏ฟฝ better performing and more sustainable versions of complex molecules traditionally sourced from plants, animals, or fossil fuels. Our platform is proven to work across scales, bridging the Valley of Death between lab and manufacturing more efficiently and more reliably to deliver the benefits of synthetic biology today.
The Mechanical Designer supports the design, development, and documentation of mechanical systems, equipment, and facilities used in biotech and pharmaceutical manufacturing environments. Working under the direction of senior engineers and project leads, this role contributes to projects from concept through installation, ensuring designs comply with GMP regulations, FDA guidelines, and applicable industry standards. The ideal candidate brings solid AutoCAD and AutoCAD 3D proficiency, a foundational mechanical background, and an eagerness to grow within a regulated manufacturing setting.
Why work at Manus:
  • Opportunity ๏ฟฝ For motivated, results-oriented team members, our growth creates opportunities for personal and professional advancement.
  • Accountability ๏ฟฝ You are given the resources you need to succeed and the freedom to make it happen; in return, we hold each other accountable for our high expectations.
  • Passion ๏ฟฝ We love what we do and enjoy working with others who feel the same way. We embrace the challenge and hard work that comes with working on the cutting edge.
Key Responsibilities
Design & Engineering
  • Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in compliance with GMP and cGMP standards.
  • Assist in the design of process equipment, piping systems, utility systems, and facility modifications for biotech/pharma manufacturing areas.
  • Produce and maintain engineering documentation including P&IDs, equipment layouts, installation drawings, BOMs, and design specifications.
  • Support design calculations, tolerance analyses, and material selections appropriate for cleanroom and regulated environments.
  • Review vendor drawings under guidance from senior staff; help verify equipment meets functional and regulatory requirements.

Project Execution
  • Support mechanical design workstreams on capital projects from initiation through commissioning and qualification (IQ/OQ).
  • Collaborate with process engineers, automation engineers, quality, and facilities to ensure mechanical designs align with operational requirements.
  • Assist with equipment procurement activities including RFQ preparation and participation in FATs/SATs.
  • Coordinate with contractors and construction teams during installation; provide field support as directed.
  • Track design deliverables, manage drawing revisions, and maintain controlled document packages in accordance with change control procedures.

Compliance & Quality
  • Ensure all mechanical designs adhere to FDA 21 CFR Part 210/211, ASME BPE, and other relevant standards under guidance from senior staff.
  • Participate in design reviews and risk assessments; document findings and follow up on assigned action items.
  • Support change control and deviation management processes from an engineering design perspective.
  • Maintain drawing and document archives in the company engineering document management system (EDMS).

Collaboration
  • Work closely with senior designers and engineers to develop technical skills and understanding of GMP design principles.
  • Follow established CAD standards, drawing templates, and best-practice documentation for the engineering team.
  • Participate actively in cross-functional project teams and communicate design status to team members and stakeholders.
Qualifications
Required
  • Associate's or Bachelor's degree in Mechanical Engineering Technology, Mechanical Design, or related field
  • 2๏ฟฝ5 years of mechanical design experience; entry-level candidates with strong internship or co-op experience will be considered
  • Proficiency in AutoCAD 2D and AutoCAD 3D; ability to produce accurate, complete design packages independently
  • Basic understanding of GMP requirements and design documentation practices in a regulated environment
  • Working knowledge of GD&T, engineering calculations, and material selection
  • Strong attention to detail and ability to manage multiple drawing deliverables concurrently

Preferred
  • Experience in a GMP-regulated biotech or pharmaceutical manufacturing environment
  • Familiarity with ASME BPE piping standards and hygienic design principles
  • Exposure to cleanroom classifications (ISO 5๏ฟฝ8) and HVAC/environmental control concepts
  • Experience with SOLIDWORKS or Inventor as a supplemental tool
  • Familiarity with engineering document management systems (EDMS)
  • Lean / continuous improvement mindset or coursework
Work Environment & Physical Requirements
  • Work is performed in a combination of office/CAD environment and active manufacturing/lab areas including cleanrooms.
  • Occasional gowning required when entering classified manufacturing spaces; adherence to site EHS and GMP protocols is mandatory.
  • May require occasional travel to vendor sites for FATs or to other company facilities.
  • Ability to lift up to 25 lbs and stand/walk on the production floor for extended periods during project support activities.

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