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Contract Biotech Jobs in Decatur, GA (NOW HIRING)

VERO BIOTECH INC

Procurement Manager

Atlanta, GA · Hybrid

At VERO Biotech, our mission is to improve the lives of patients by developing innovative ... Serve as procurement liaison for contract manufacturing organizations (CMOs) and external ...

CorDx

Senior BD Manager (Atlanta)

Atlanta, GA

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... Support contract negotiations, licensing discussions, and partnership agreements. * Ensure smooth ...

CorDx

Senior BD Manager (Atlanta)

Atlanta, GA · On-site

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Support contract negotiations, licensing discussions, and partnership agreements. * Ensure smooth ...

CorDx

Senior BD Manager (Atlanta)

Atlanta, GA · On-site

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... Support contract negotiations, licensing discussions, and partnership agreements. * Ensure smooth ...

CorDx

Supply Chain Manager

Atlanta, GA

$80K - $120K/yr

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 ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$80K - $120K/yr

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 ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$80K - $120K/yr

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 ...

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$15

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How much do contract biotech jobs pay per hour?

As of May 30, 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, and why are they important?

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 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 and what do they do?

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 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 the most commonly searched types of Biotech jobs in Decatur, GA? The most popular types of Biotech jobs in Decatur, GA are:
What are popular job titles related to Contract Biotech jobs in Decatur, GA? For Contract Biotech jobs in Decatur, GA, the most frequently searched job titles 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:
Contract Biotech jobs near you

Commercial Contracts Specialist

Kuros Biosciences, Inc.

Sandy Springs, GA • On-site

Full-time

Posted 2 days ago

Job description

Overview:
The Commercial Contracts Specialist supports the company's commercial, legal, and financial operations by managing the drafting, review, negotiation, and execution of commercial agreements. Reporting to the Corporate Attorney and working in close functional alignment with the VP of Finance and Sales leadership, this position serves as the primary contracting partner for the Sales organization.
This role ensures contracts are accurate, compliant, financially aligned, and processed efficiently through the company's Contract Lifecycle Management (CLM) system. The Specialist is essential to maintaining standardized contracting practices and supporting the company's growth in the medical device industry. This is a full-time,hybrid position.
Key Responsibilities:
Contract Drafting, Review, and Negotiation
  • Draft, review, and negotiate commercial agreements including sales agreements, distributor agreements, vendor contracts, NDAs, and pricing/rebate agreements.
  • Work within approved templates and playbooks; escalate non-standard or high-risk terms to the Corporate Attorney.
  • Provide timely support to Sales leadership with contract revisions and customer-facing documentation.

Contract Lifecycle Management
  • Administer the company's CLM platform, including template updates, workflow routing, reporting, and system maintenance.
  • Maintain accurate contract records, version control, audit trails, and document retention.

Finance & Pricing Coordination
  • Partner with Finance to validate pricing structures, rebate terms, discount programs, payment terms, and revenue-recognition considerations.
  • Ensure all financial terms are accurately incorporated into customer and vendor agreements.

Regulatory & Policy Compliance
  • Ensure contracts adhere to medical device and life sciences regulatory requirements, including:
    • Anti-Kickback Statute
    • Open Payments/Sunshine Act
    • Anti-corruption (FCPA and similar frameworks)
    • FDA-related quality, complaint, labeling, and distribution obligations
  • Support internal compliance reviews and audits related to contracting practices.

Cross-Functional Collaboration
  • Act as the primary contracting liaison for Sales, Legal, Finance, Operations, and other stakeholders.
  • Communicate contract requirements, timelines, risks, and necessary approvals across teams.

Process & Template Improvement
  • Assist with updating templates, clause libraries, and contract playbooks.
  • Identify opportunities to improve contracting workflows and reduce cycle times.
  • Promote consistency and efficiency across the contracting function.

Qualifications:
Required
  • Bachelor's degree in Business, Legal Studies, Finance, or a related field.
  • 3-5 years of commercial contracting experience in the medical device, life sciences, or pharmaceutical industry.
  • Experience drafting, reviewing, and negotiating commercial agreements.
  • Familiarity with healthcare compliance requirements and regulatory frameworks.
  • Experience with Contract Lifecycle Management (CLM) systems.
  • Strong attention to detail and ability to manage multiple priorities in a fast-paced environment.
  • Excellent written and verbal communication skills.

Preferred
  • Paralegal certification or equivalent legal training.
  • Experience supporting commercial or field sales teams.
  • Understanding of international medical device regulatory considerations.

Key Competencies
  • Contract negotiation and redlining
  • CLM system administration
  • Regulatory and compliance awareness
  • Cross-functional communication and collaboration
  • Process improvement and problem-solving
  • Ability to manage complexity and prioritize effectively

Travel Requirement:
  • Ability to travel domestic and international as needed

Physical Requirements and Work Conditions
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
  • Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.
  • Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.
  • Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.
  • Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license.

Specific requirements may vary by role. Contact an HR representative for details related to the position.
Our credentials
Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.
To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.
  • Listing on the SIX Swiss Exchange under the symbol KURN since 2016
  • A commercial & research footprint that spans >20 markets
  • Dozens of clinical and scientific expert Advisers
  • >25 orthobiologics-related patents
  • >400 patients evaluated in Level I, randomized controlled clinical trials
  • >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1
  • Published Level I evidence published in Spine

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.

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