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Biotech Consultant Jobs in Raleigh, NC (NOW HIRING)

Zifo

Principal CQV Consultant

Cary, NC · Hybrid

Act as the primary CQV SME during pre-sales discussions with pharma/biotech clients. * Identify new ... Advise and guide onsite/remote validation consultants on qualification strategy, deviations, test ...

NNE AS

Advanced CQV Engineer - Clayton NC

Clayton, NC · On-site

At NNE, we help pharmaceutical and biotech companies design and deliver the facilities and processes that improve lives. As an Advanced CQV Consultant, you will lead commissioning, qualification, and ...

Valspec

ERP (D365) Validation Consultant

Raleigh, NC · On-site +1

We partner with a variety of sectors, including pharmaceutical, biotech, manufacturing, and other regulated industries. Position Summary: As a Microsoft D365 ERP Validation Consultant with cloud ...

Valspec

ERP (D365) Validation Consultant

Durham, NC · On-site +1

We partner with a variety of sectors, including pharmaceutical, biotech, manufacturing, and other regulated industries. Position Summary: As a Microsoft D365 ERP Validation Consultant with cloud ...

Grifols

Refrigeration Consultant

Clayton, NC · On-site

$85K - $120K/yr

Experience in a Pharmaceutical / Biotech environment a plus Equivalency: Depending on the area of ... Consultant role based is $85k - 120k per year. Additionally, the position is eligible to ...

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All JobsBiotech Consultant JobsBiotech Consultant Jobs in Raleigh, NC

Biotech Consultant information

See Raleigh, NC salary details

$10

$40

$84

How much do biotech consultant jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotech consultant in Raleigh, NC is $40.39, according to ZipRecruiter salary data. Most workers in this role earn between $28.51 and $48.12 per hour, depending on experience, location, and employer.

What is a biotech consultant?

Biotech consultants are professionals who provide expert advice and strategic guidance to organizations in the biotechnology sector. They assist companies with areas like research and development, regulatory compliance, market analysis, and business development. Biotech consultants often draw on scientific expertise and industry experience to help clients solve complex problems, improve processes, and bring new products to market. Their services are valuable to startups, established firms, and investors looking to navigate the rapidly evolving biotech landscape.

What does a biotech consultant do?

A biotech consultant advises managers at a biotechnology company on ways to improve efficiency or how to develop new products and services. As a biotech consultant, you possess in-depth knowledge of emerging therapies, equipment, and products in the biotech industry. Your job duties include observing current production cycles, reviewing financial data, inspecting the equipment, and determining what areas need improvement. Once you have created recommendations, you present your findings to the company and plan strategies to implement effective changes within a department or throughout the organization. Some biotech consultants work for a consulting firm, while others are independent contractors who may work with one or several clients at a time.

What are the key skills and qualifications needed to thrive as a biotech consultant, and why are they important?

To thrive as a Biotech Consultant, you need a strong background in life sciences or biotechnology, often supported by an advanced degree and relevant industry experience. Familiarity with data analysis software, regulatory databases, and project management tools is typically required. Outstanding communication, problem-solving, and client management skills set top consultants apart. These abilities are crucial for delivering strategic insights, ensuring regulatory compliance, and fostering strong client relationships in a rapidly evolving field.

What types of clients and projects do biotech consultants typically work with, and how does this influence their daily responsibilities?

Biotech Consultants often collaborate with a wide range of clients, including startups, pharmaceutical companies, research institutions, and investors. This diversity means their daily responsibilities can vary significantly, from conducting market analysis and regulatory strategy development to supporting product commercialization or advising on clinical trial design. The role is highly collaborative, requiring frequent meetings with client teams, cross-functional internal experts, and sometimes regulatory authorities. This dynamic environment fosters continual learning and offers exposure to cutting-edge scientific advancements while also demanding strong project management and communication skills.

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

AspectBiotech ConsultantBiotech Research Associate
Required CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; often some industry experienceBachelor's or Master's in Biology, Biotechnology, or related fields; laboratory experience preferred
Work EnvironmentConsulting firms, client sites, corporate officesResearch laboratories, academic institutions, biotech companies
Employer & Industry UsageConsulting firms, biotech companies, pharma firmsResearch institutions, biotech and pharma companies

Biotech Consultants focus on advising clients on biotech strategies, market analysis, and project management, often working in a consulting environment. In contrast, Biotech Research Associates primarily conduct laboratory research, experiments, and data analysis within research labs. While both roles require a background in life sciences, their work settings and daily tasks differ significantly.

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Biotech Consultant jobs near you
Infographic showing various Biotech Consultant job openings in Raleigh, NC as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $84,017 per year, or $40.4 per hour.

Benchling Solutions Consultant

PPG US ProPharma Group, LLC

Raleigh, NC • On-site

$90 - $150/hr

Other

Posted 4 days ago

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Key responsibilities include:

  • Benchling implementation and managed service support: Providing Benchling related project scoping, requirements gathering, documentation generation, and overall system assessment. This includes any new requirements and alignment of these to Benchling capabilities, to empower expansion of the system to various use cases not currently supported by the Benchling platform after the conclusion of the initial implementation.
  • Maintenance and support of Client Benchling Test and Production Environments Providing data model (registry and result) configuration and updates Updating existing and creating new notebook templates and workflows Updating existing and creating new recipe schema (Bioprocess module) Updating existing and creating new inventory hierarchies and schema Updating existing and creating new Insights dashboards and analysis. Updating existing and creating new automation runs, using the Connect Module Updating and creating Benchling Label templates. Maintenance and generating as needed client tailored training material for new hires as well as existing Benchling end user training.
  • Spreadsheet based legacy data migrations and imports into Benchling.
  • Configuration of the Benchling in vivo software (this is a nice to have right now, but if we get Moderna would be required)
  • Understanding and use of Benchling APIs for integrations is a bonus.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

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