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Biotech Consulting Jobs in Ohio (NOW HIRING)

Visa Hunt

$150 - $210/hr

Generate new CDx regulatory consulting opportunities through established relationships with pharmaceutical, biotechnology, diagnostic, laboratory, and precision medicine stakeholders. * Partner with ...

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As a global provider of clinical research services, healthcare intelligence, and consulting solutions, we partner with pharmaceutical, biotechnology, and medical device organizations to accelerate ...

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Mix Talent

Associate Recruiter

Columbus, OH · On-site

$42K - $51K/yr

A strong foundation in consultative recruiting and talent strategy * Exposure to high-level client interactions and decision-making * A network of professionals across the biotech and pharmaceutical ...

Mix Talent LLC

Associate Recruiter

Columbus, OH

$42K - $51K/yr

A strong foundation in consultative recruiting and talent strategy * Exposure to high-level client interactions and decision-making * A network of professionals across the biotech and pharmaceutical ...

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Biotech Consulting information

See Ohio salary details

$20.4K

$76.8K

$154K

How much do biotech consulting jobs pay per year?

As of Aug 22, 2026, the average yearly pay for biotech consulting in Ohio is $76,842.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,500.00 and $100,300.00 per year, depending on experience, location, and employer.

What is biotech consulting?

Biotech consulting is a specialized professional service that provides expert advice and guidance to biotechnology companies and organizations. Consultants help clients with areas like regulatory compliance, research and development strategies, market analysis, product commercialization, and fundraising. They leverage industry experience and technical expertise to solve complex challenges, improve processes, and support business growth in the biotech sector. Biotech consultants often work with startups, established companies, investors, and academic institutions.

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

To thrive as a Biotech Consultant, a solid background in life sciences or biotechnology, often with an advanced degree (e.g., MSc or PhD), and business acumen are essential. Familiarity with data analysis tools, regulatory frameworks, and industry-standard software like SAS or R is typically required. Outstanding problem-solving, communication, and client management skills help consultants build trust and deliver actionable insights. These competencies are vital for effectively advising clients, navigating complex projects, and driving innovation in the rapidly evolving biotech sector.

What are some common challenges faced by professionals in biotech consulting, and how can they be navigated?

Professionals in biotech consulting often encounter challenges such as staying updated with rapidly evolving scientific developments, managing diverse client expectations, and balancing multiple projects with tight deadlines. To navigate these challenges, consultants must prioritize ongoing education, leverage strong project management skills, and foster clear communication with both clients and internal teams. Building a robust professional network and maintaining adaptability are also key strategies for success in this dynamic field.

Does biotech consulting pay well?

Biotech consulting typically offers competitive salaries that vary based on experience, education, and location. Entry-level consultants may earn starting salaries around $70,000 to $90,000 annually, with experienced professionals earning over $150,000, especially with specialized skills or advanced degrees. Bonuses and benefits are also common in this field.

How to get into biotech consulting?

To enter biotech consulting, candidates typically need a strong background in life sciences, such as a degree in biology, chemistry, or related fields, along with experience in the biotech or pharmaceutical industry. Developing skills in data analysis, project management, and understanding regulatory environments can be beneficial, and some roles may require consulting or business experience. Gaining relevant certifications or training in consulting methodologies can also improve prospects.

What does a biotech consulting do?

A biotech consultant provides expert advice to biotechnology companies on research, development, regulatory compliance, and commercialization strategies. They analyze scientific data, help optimize processes, and support product development using industry knowledge and technical skills. This role often requires understanding of biotech tools, regulations, and project management.

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

The most popular types of Biotech Consulting jobs in Ohio are:

What are popular job titles related to Biotech Consulting jobs in Ohio?

For Biotech Consulting jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Biotech Consulting jobs in Ohio look for?

The top searched job categories for Biotech Consulting jobs in Ohio are:

What cities in Ohio are hiring for Biotech Consulting jobs?

Cities in Ohio with the most Biotech Consulting job openings:

Biotech Consulting jobs near you
Infographic showing various Biotech Consulting job openings in Ohio as of August 2026, with employment types broken down into 1% Internship, 87% Full Time, 7% Part Time, and 5% Contract. Highlights an 83% Physical, 6% Hybrid, and 11% Remote job distribution, with an average salary of $76,842 per year, or $36.9 per hour.

Senior Packaging Validation Engineer, Biotech GMP Final Drug Product

3 Key Consulting

New Albany, OH • On-site

$100K - $137K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Senior Validation Engineer, Biotech GMP Final Drug Product3 Key Consulting is hiring! We are recruiting a Senior Validation Engineer for a consulting engagement with our direct client, a leading global biotechnology company.The Senior Validation Engineer position reports into the Sr. Manager of Validation. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations.Location Options: 100% Site Presence Required. The position is expected to travel for approximately 10%.Job Description & ResponsibilitiesThe Senior Validation Engineering will support the development and implementation of automated and semi-automated combination product assembly equipment initiatives as part of the Finished Drug Product (FDP) product portfolio at the Ohio manufacturing site. The position is a key role in the Process Development team where the candidate must manage and/or apply extensive technical expertise (characterization, validation and troubleshooting) in the validation of combination products. This position also requires the application of advance and diverse engineering principles to more than one area of engineering (process, unit operations, equipment, devices and materials) in complex process optimization, scale up and manufacturing support projects.Key responsibilities will include supporting the packaging C&Q activities of the product portfolio to AOH. Additional responsibilities will include the provision of technical operations support for the continuous improvement of device assembly and packaging line capacity and performance, and advisory of technical improvement projects. The Sr. Validation Engineer must ensure effective communication throughout the Ohio commercial site and network with all stakeholders and deliver on technical deliverables.RelationshipThe Senior Validation Engineering is expected to build on the network expertise across the company commercial and clinical operations for product assembly, label and packaging. The position is expected to leverage this network in support of GMP technical expertise, performance trending, equipment standardization and troubleshooting/process.The Successful Candidate Will Have:Knowledge of high-speed, highly automated secondary packaging operationsKnowledge of the validation of equipment such as PFS assembly, cartoners, vision systemsExperience in writing protocolsExperience in executing protocolsCapable of executing multiple projectsCommunication skills and ability to work with other peopleBring innovative solutions for continuous process improvementExperience with KneatExperience with MiniTab is a plusTop Must Have Skill Sets:Packaging validation experienceKnowledge of packaging equipmentProtocol generation and executionDay to Day Responsibilities:Writing and executing validation protocols.Value proposition: Unique industry opportunity NetworkingBasic Qualifications: Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experienceWhy is the Position Open? Supplement additional workload on teamInterview Process: Initial screening with hiring manager Final interview panel with 3 interviewers

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