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Biologics Consulting Group Jobs (NOW HIRING)

Senior Biologist

Los Angeles, CA · Remote

$85K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Santa Ana, Los Angeles, San Diego Chambers Group, Inc. is an environmental consulting firm ... Position Summary The Senior Biologist is responsible for leading and delivering technical ...

Associate Scientific Strategy Consultant

Boston, MA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... American consulting group wherein key accountabilities include driving project elucidation ... Bachelor's or Master's degree in a relevant scientific discipline such as biology, chemistry, chem ...

Associate Scientific Strategy Consultant

Boston, MA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... American consulting group wherein key accountabilities include driving project elucidation ... Bachelor's or Master's degree in a relevant scientific discipline such as biology, chemistry, chem ...

Associate Scientific Strategy Consultant

Boston, MA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... American consulting group wherein key accountabilities include driving project elucidation ... Bachelor's or Master's degree in a relevant scientific discipline such as biology, chemistry, chem ...

Field Biologist

Washington, DC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Launched by former Big 4 Management Consultants; our multidisciplinary teams bring together the ... Group Health Insurance Benefits: Medical: ProSidian partners with BC/BS, to offer a range of ...

EAS Consulting Group - A regulatory consulting firm offering expert guidance, training, and ... Train staff on proper handling of biological or hazardous materials * Maintain documentation for ...

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Biologics Consulting Group information

See salary details

$24K

$72.9K

$156K

How much do biologics consulting group jobs pay per year?

As of Aug 15, 2026, the average yearly pay for biologics consulting group in the United States is $72,851.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,000.00 and $90,000.00 per year, depending on experience, location, and employer.

How does collaboration typically work within a Biologics Consulting Group and with external clients?

Team members in a Biologics Consulting Group often collaborate closely with internal experts in regulatory affairs, clinical development, and manufacturing to provide comprehensive guidance for clients. Regular project meetings and cross-functional discussions are common, ensuring that client challenges are addressed from multiple perspectives. Externally, consultants work directly with clients—such as biotech firms and pharmaceutical companies—to understand their development goals and provide tailored regulatory or scientific advice. Strong communication and teamwork skills are essential, as projects frequently involve coordinating with both internal colleagues and client teams to achieve successful outcomes.

What is the difference between Biologics Consulting Group vs Bioprocess Engineer?

AspectBiologics Consulting GroupBioprocess Engineer
CredentialsTypically requires life sciences degree, industry experience, and consulting expertiseRequires degree in bioengineering, chemical engineering, or related field; often with industry experience
Work EnvironmentConsulting firms, client sites, project-basedBiotech or pharmaceutical manufacturing facilities, laboratories
Industry UsageUsed by consulting firms providing strategic and technical adviceEmployed directly by biotech or pharma companies to develop and optimize bioprocesses

While both roles involve bioprocessing knowledge, Biologics Consulting Group professionals focus on providing expert advice across multiple clients, whereas Bioprocess Engineers work within companies to develop and improve manufacturing processes. The roles overlap in technical skills but differ in work setting and scope.

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

To thrive as a Biologics Consultant, you need a deep understanding of biologics development, regulatory affairs, and quality assurance, typically backed by a degree in life sciences or a related field. Familiarity with FDA and EMA regulations, Good Manufacturing Practices (GMP), and experience using regulatory submission systems is essential. Strong analytical thinking, problem-solving, and clear communication skills help you effectively advise clients and navigate complex regulatory environments. These competencies are crucial for ensuring compliance, facilitating product approvals, and supporting client success in the highly regulated biologics sector.

What is Biologics Consulting Group?

Biologics Consulting Group is a firm that provides regulatory and product development consulting services to companies in the biotechnology, pharmaceutical, and medical device industries. They help clients navigate the complex regulatory environment for biologics, drugs, and medical devices, offering expertise in areas such as FDA submissions, clinical trial design, and compliance. Their team includes former FDA officials, scientists, and industry experts who guide clients through every stage of product development, from preclinical research to post-market activities.
More about Biologics Consulting Group jobs
Infographic showing various Biologics Consulting Group job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $72,851 per year, or $35 per hour.

Regulatory Affairs Business Unit Leader

BIOLOGICS CONSULTING GROUP INC

Alexandria, VA • Remote

$170K - $195K/yr

Full-time

Posted 4 days ago


Job description

Regulatory Affairs Business Unit Leader

(RA Strategy and Project Management)


Position Summary:

The role includes leading the Regulatory Affairs team, responsibility for all team financial KPIs, and providing knowledge, experience, business development support, and direction to achieve company and business unit goals. The incumbent will foster a collaborative, team-oriented environment, ensuring an overall ‘culture of quality’ in the execution of services provided to clients. The Business Unit Leader is responsible for driving performance, achieving goals, and advancing growth strategies. This position requires a balance of client/opportunity oversight, quality management, and people management, along with strategic business development and marketing acumen, with support from regulatory affairs team members, in line with the Company's growth objectives as defined by Management (65% of time).Billable/consulting duties (35% time) will include providing direct client consultation and delivering high-level strategic thinking with operational execution across all stages of product development, registration, and post-marketing.

This individual will lead a team of strategic regulatory experts and experienced operational regulatory project managers at all levels. The team primarily supports large cross-functional projects that engage specialists from other business units, including CMC, clinical, nonclinical, regulatory operations, and medical devices, as well as external partners.

Biologics Consulting Group, Inc. works with medical devices, biologics, and pharmaceutical companies to advance patient health.


Responsibilities:

· Lead and mentor a team of regulatory affairs strategy and project managers with a focus on high-quality and timely delivery of regulatory submissions spanning INDs, BLAs, NDAs, etc.

· Develop and execute an annual strategic business plan for the regulatory affairs consulting practice, ensuring alignment with company goals

· Identify new business opportunities, expand the customer base, and build long-term client relationships

· Monitor industry trends, regulatory changes, and emerging market needs to keep services relevant and competitive

· Serve as the primary point of contact for key clients, providing expert guidance on complex regulatory strategies

· Lead client presentations, negotiations, and communications to maintain high levels of satisfaction and loyalty

· Develop strategy and implement an action plan for capacity planning and growth, including recruitment.

· Work with other team leaders to facilitate the timely identification of resources required to support single and multidisciplinary projects where appropriate

· Collaborate with BD, HR, the Executive team and other group leaders in identifying best practices for onboarding, recruiting, staff growth and business development to meet business goals.

· Demonstrated leadership ability including ability to create a positive and collegial culture and motivate the regulatory affairs team to perform effectively

· Facilitate successful project/program launches while ensuring that the programs run smoothly and in compliance with agreed-upon timelines and budgets.

· Lead the execution of regulatory plans, ensuring alignment between day-to-day operations and broader strategic objectives across global programs.

· Identify and propose innovative regulatory pathways and planning scenarios that align with global regulatory expectations and business objectives.


Requirements:

· Bachelor’s degree in a scientific, regulatory, or engineering discipline; an advanced degree is highly preferred.

· Minimum of 10 years of progressive experience in the pharmaceutical, biotechnology, or related life sciences industry, with at least 5 years in a leadership role in regulatory strategy or regulatory program management

· Proven ability to partner on regulatory strategy and lead execution across all stages of product development, including PIND/IND/BLA/MAA/NDA/ANDA submissions, global registration, and post-marketing activities

· Deep understanding of U.S. regulatory requirements with working knowledge of international (ex-U.S.) regulations and agency expectations, including global regulatory pathways, expedited programs, and dossier structures.

· Exceptional communication and influencing skills, with the ability to synthesize complex regulatory information and translate it into clear recommendations for senior leadership and global stakeholders.

· Demonstrated ability to develop, implement, refine, and leverage project management tools and best practices to enhance visibility, efficiency, cross-functional alignment, and meeting effectiveness across regulatory affairs and project teams.

· Demonstrated experience facilitating cross-functional team meetings, driving structured agendas, documenting decisions and actions, and maintaining strong meeting hygiene and team accountability in a matrixed environment.

· Expert skills required for Smartsheet (Regulatory Activity and Submissions Project Plans) and Microsoft Office Suite

· Expert in creating visuals using PPT generated from timeline integration tools (ie, One Pager, Office Timeline Pro, etc.)

· Must exercise rapid learning ability, attention to detail, excellent computer skills, excellent oral and written communication skills, team player, organized analytical thinker with a high level of energy and self-motivation

· Demonstrated versatility in conflict resolution, problem solving, and working effectively as part of a cross-functional organization.

· Strategic thinking and problem-solving skills, with a strong focus on client satisfaction and business growth


Key Performance Indicators:

· Contribution to team revenue and overall business development

· Implementation of scalable project management system across team

· Quality and timeliness of client deliverables

· Strengths of client relationships and client satisfaction

· Mentorship and development of junior and mid-level staff

· Contributions to thought leadership and professional visibility

· Demonstrated teamwork and leadership capabilities


Essential Skills:

Proficient in Microsoft Office Suite, keyboarding skills, strong documentation skills, math aptitude, diplomacy and leadership skills, professionalism, time management, ability to multitask, able to work independently as well as collaboratively, and able to maintain confidentiality.


The listed requirements are representative of the knowledge, skills, and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.