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$10

$41

$87

How much do biotech consultant jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for biotech consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What does a biotech consultant do?

A biotech consultant provides expert advice to biotechnology companies on research, development, regulatory compliance, and commercialization strategies. They analyze scientific data, recommend process improvements, and help clients navigate industry regulations, often using tools like project management software and scientific literature. Strong knowledge of biology, chemistry, and industry standards is essential for this role.

What are biotech consultants?

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 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.

How much does a biotech consultant earn?

Biotech consultants typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Senior consultants or those with specialized skills can earn higher salaries, often exceeding $150,000 with bonuses and benefits included.

What are the big 4 in biotech?

The 'Big 4' in biotech typically refers to the four major pharmaceutical and biotech companies: Johnson & Johnson, Roche, Pfizer, and Novartis. These companies lead the industry in research, development, and commercialization of biotech products, often requiring biotech consultants to have expertise in drug development, regulatory processes, and industry trends.

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 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.

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.

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 if they have specialized knowledge or advanced degrees. Bonuses and benefits can also contribute to overall compensation in this field.
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Biotech Consultant jobs near you
Engineer, Biotech Equipment and Facilities (JP11899)

Engineer, Biotech Equipment and Facilities (JP11899)

3 Key Consulting

Thousand Oaks, CA • On-site

$38 - $42/hr

Other

Posted 9 days ago

Job description

Job Title: Engineer, Biotech Equipment and Facilities (JP11899)
Location: Thousand Oaks, CA. 91320
Business Unit: F&E Drug Substance Supply
Employment Type: Contract
Duration: 1+ year(s) (with possible extensions)
Rate: $38 - $42/hour W2
Posting Date: 10/18/23
Notes: Only qualified candidates need apply. Fully onsite
3 Key Consulting is recruiting an Engineer, Biotech Equipment and Facilities for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
This engineering position supports manufacturing activities associated with cGMP equipment and facilities at client in Thousand Oaks. The engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee the operation and reliability of equipment while driving safety and quality compliance. The engineer will support the department and capital projects and provide data to support business cases and long term strategy. The Engineer role will provide direct engineering technical support as follows:
  • Model leadership behaviors and positive values to create a positive working environment.
  • Be individually accountable for the consistent equipment performance
  • Be accountable for assigned deliverables on key capital projects
  • Suggest design modifications to address risks and design in quality and safety.
  • Provide oversight for verification deliverables developed by outsourced/contract verification staff.
  • Act as a liaison between Engineering and Quality Assurance during project planning, execution, and closeout
  • Ensure that validation protocols are executed and documented in accordance with cGMP good documentation and safety compliant practices.
  • Ensure safety during commissioning, validation, maintenance, and manufacturing activities
  • Related Activities:
  • Participate or lead, when required, multidisciplinary site teams, e.g. Cross Functional Team, Root Cause Analysis lead.
  • Support Lean Transformation and Excellence in Operations process improvement by leading, supporting, and documenting improvement opportunities to reduce cost, improve safety/quality, or improve speed.
  • Provide ad hoc technical support and guidance for manufacturing and maintenance
  • Provide coaching and guidance to project teams and engineers using risk-based approaches
  • Defend the equipment-specific calibration, maintenance, & validation as required during regulatory inspections
  • Participate in internal audits and assess in conjunction with quality assurance
  • Assist in developing and maintaining business metric performance

Top Must Have Skill Sets:
  • Fundamental client Leadership and Values -preferable to see former client workers
  • Good Communication / Safety / Quality Focused
  • Fundamental Technical Knowledge

Day to Day Responsibilities:
  • Support Epogen Commercial manufacturing equipment
  • Model leadership behaviors and positive values to create a positive working environment.
  • Be individually accountable for the consistent equipment performance
  • Be accountable for assigned deliverables on key capital projects
  • Suggest design modifications to address risks and design in quality and safety.
  • Provide oversight for verification deliverables developed by outsourced/contract verification staff.
  • Act as a liaison between Engineering and Quality Assurance during project planning, execution, and closeout
  • Ensure that validation protocols are executed and documented in accordance with cGMP good documentation and safety compliant practices.
  • Ensure safety during commissioning, validation, maintenance, and manufacturing activities

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
  • Bachelor's degree in engineering or another science-related field
  • 7+ years of relevant work experience with 5+ years' experience in operations/manufacturing environment
  • Direct experience with regulated environments (FDA, OSHA, EPA, etc.)
  • Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, clean utilities, facilities, instruments, and equipment
  • Experience implementing risk-based verification on major GMP process equipment / automation projects, including validation protocol development and execution
  • Experience with combination product / medical device quality systems verification
  • Process equipment knowledge - basic principles of cell culture, fermentation, purification, filling
  • Process automation knowledge - fundamental understanding of automation infrastructure
  • Knowledge of Delta V, Rockwell, and Plant Information Systems is a plus
  • Strong communication and technical writing skills
  • Strengths in facilitation and collaboration / networking
  • Experience in developing SOPs and delivering training
  • Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making
  • Basic understanding of process improvement methodologies to mature and improve business performance (examples: PDCA, LEAN, Six Sigma, etc.)

Red Flags:
  • Safety not recognized as top priority
  • Poor communication
  • Has issues under stressful situations
  • Blames other for negative situations

Interview Process:
One phone screen/onsite interview.
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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