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Contract Biotech Jobs in Decatur, GA (NOW HIRING)

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

Prepare renewal contracts and order forms, ensuring accuracy in pricing, uplift, and co ... such as finance, healthcare, biotech and pharmaceuticals, over10,000 highly specialized ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... The Pricing and Contracts Manager is responsible for leading commercial deal support across pricing ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Manage supplier relationships, negotiate contracts, and evaluate performance for quality and cost ...

Contract Job Location: Peachtree Corners, GA Work Schedule: On-site Pay Rate: $49, Based on ... Minimum 1-2 years of experience in biotech or medical device organization preferred * Curriculum ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Manage supplier relationships, negotiate contracts, and evaluate performance for quality and cost ...

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... Manage supplier relationships, negotiate contracts, and evaluate performance for quality and cost ...

Packer

Norcross, GA · On-site

$15 - $17/hr

The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and ...

Life Sciences Tutor

Marietta, GA · Remote

$18 - $40/hr

... biotechnology career applications. * Curriculum Awareness & Adaptive Instruction: Familiar with ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

Showing results 41-60

Contract Biotech information

See Decatur, GA salary details

$15

$35

$53

How much do contract biotech jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for contract biotech in Decatur, GA is $35.48, according to ZipRecruiter salary data. Most workers in this role earn between $25.82 and $42.69 per hour, depending on experience, location, and employer.

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

To thrive as a Contract Biotech professional, you need a strong background in biological sciences, laboratory techniques, and data analysis, usually supported by a relevant degree in biotechnology or a related field. Familiarity with lab information management systems (LIMS), molecular biology tools, and compliance regulations like GLP or GMP is typically required. Strong problem-solving, attention to detail, and effective communication skills are essential for collaborating with clients and team members. These competencies ensure accurate project delivery, adherence to regulatory standards, and successful client relationships in a dynamic biotech environment.

What is the difference between Contract Biotech vs Contract Research Associate?

AspectContract BiotechContract Research Associate
CredentialsBachelor's or Master's in Life Sciences, relevant experienceBachelor's or Master's in Life Sciences, laboratory skills
Work EnvironmentBiotech companies, labs, manufacturing facilitiesResearch labs, clinical trial sites, biotech firms
Employer & Industry UsageBiotech firms, pharmaceutical companies, contract research organizationsResearch organizations, biotech companies, clinical research settings

Contract Biotech roles typically involve working on product development, manufacturing, or process optimization within biotech companies, often requiring technical expertise. Contract Research Associates focus on supporting clinical trials and research studies, performing experiments, and data collection. While both roles are contract-based and in the biotech industry, Contract Biotech positions emphasize technical and manufacturing skills, whereas Contract Research Associate roles center on research and clinical support.

What are some common challenges faced by contract biotech professionals, and how can they be addressed?

Contract biotech professionals often encounter challenges related to adapting quickly to new organizational cultures and workflows, as they may work with multiple clients or projects in short timeframes. Balancing the expectations of different stakeholders while ensuring compliance with regulatory standards can also be demanding. To address these challenges, it's important to develop strong communication skills, be proactive in understanding project goals, and stay current with industry regulations. Building a network within the biotech community can also help with knowledge-sharing and support.

What is a contract biotech?

A Contract Biotech refers to a company or professional that provides biotechnology research, development, and manufacturing services to other organizations on a contractual basis. These services can include laboratory research, drug development, clinical trials, and production of biological products. Contract Biotech organizations help pharmaceutical companies, academic institutions, and startups accelerate their projects without needing to build extensive in-house capabilities. This allows clients to access specialized expertise and facilities, manage costs, and bring products to market more efficiently.
What are the most commonly searched types of Biotech jobs in Decatur, GA? The most popular types of Biotech jobs in Decatur, GA are:
What job categories do people searching Contract Biotech jobs in Decatur, GA look for? The top searched job categories for Contract Biotech jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Contract Biotech jobs? Cities near Decatur, GA with the most Contract Biotech job openings:
Infographic showing various Contract Biotech job openings in Decatur, GA as of August 2026, with employment types broken down into 72% Full Time, 8% Temporary, and 20% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $73,796 per year, or $35.5 per hour.

Validation Engineer

Pinnaql

Atlanta, GA • On-site

Full-time

Re-posted 28 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Validation Engineer

Description:
The role demands deep technical expertise across the full validation lifecycle - including URS development, FAT/SAT execution, and Computer System Validation (CSV) - as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.
Key Responsibilities:
  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:
  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.