Sr. Consultant, CMC

Socket.dev; Virginia (MN); On-site; USD 130,000 - 190,000; Full time

Job summary

Biologics Consulting Group, Inc. seeks a Senior Consultant, CMC to lead complex CMC and FDA regulatory projects, manage client relationships, and mentor junior staff.

You will oversee scientific quality, contribute to business development, and provide strategic guidance from early development through commercialization, ensuring timely, compliant deliverables across accounts. You will also guide regulatory strategy, QA oversight, and GMP expectations, supporting product launches and

Qualifications

• Ph.D. strongly preferred with 5–7 years of industry, consulting, and/or FDA experience.
• Alternatively, a master’s degree with at least ten years of relevant experience.
• Prior consulting experience and/or direct FDA or other regulatory interaction is strongly preferred.
• Experience in process development, validation and biomanufacturing of biologic substance/drug product is strongly preferred.
• Knowledge of GMP regulatory expectations and EMA pathways is advantageous.

Responsibilities

• Serve as the CMC subject‑matter expert for technical, quality and regulatory consulting needs.
• Lead or support projects ensuring quality and timely delivery for client work.
• Provide consultation to advise on approaches that advance product development from early development through commercialization.
• Develop high‑quality regulatory documents, technical reports, and literature reviews.
• Provide quality control for work authored by junior team members and ensure deliverables meet client/regulatory expectations.
• Delegate tasks across junior staff to optimize workflow and promote development.
• Independently manage client relationships and act as a key contact for project execution and issue resolution.
• Support business development by identifying opportunities within existing accounts and contributing to proposals.
• Mentor and coach junior staff, sharing expertise in project execution, scientific writing, and regulatory knowledge.
• Engage in thought leadership to increase visibility as a subject matter expert.

Skills

Leadership

Scientific writing

Regulatory knowledge

Mentoring

Client relations

Project management

Communication

Education

Ph.D. in biotechnology or related field

Master's degree in related disciplines

Tools

Microsoft Office

Job description

Senior Consultant, CMC

Position Summary

The Senior Consultant, CMC is a mid- to senior-level role responsible for leading complex CMC related scientific and U.S. Food and Drug Administration (FDA) regulatory consulting projects, managing client relationships, and contributing to business development activities. The position requires the ability to consult independently, provide scientific and strategic oversight on client work, and mentor junior staff. The Senior Consultant contributes directly to client deliverables while also ensuring quality and consistency in project execution. This role plays a key part in strengthening client partnerships, expanding existing accounts, and supporting organizational growth through thought leadership, professional development, and the development of junior team members.

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

Responsibilities

• Serve as the CMC subject‑matter expert in CMC for technical, quality and regulatory consulting needs.
• Serve as the senior project leader or project support, as needed for client delivery of project work.
• As senior project leader is accountable for quality and delivery of client work while providing direct consultation to advise them on best approaches that will effectively advance product development efforts including ongoing support from early development through clinical stages and commercialization.
• Contribute to the development of high-quality deliverables, including regulatory documents, technical reports, and literature reviews.
• Provide quality control for work authored by junior team members and ensure deliverables meet client and regulatory expectations.

• Delegate tasks appropriately across junior team members to optimize workflow and promote development of junior staff.

• Independently manage client relationships and act as a key point of contact for project execution and issue resolution for projects on which the senior project leader role is held.
• Support business development efforts by identifying opportunities within existing accounts and identifying new opportunities, as well as participating in proposal development and review.
• Actively participate in mentoring and coaching activities for junior-level team members, sharing expertise in project execution, scientific writing, and regulatory knowledge.
• Engage in thought leadership efforts to increase visibility as a subject matter expert in key areas of practice.
• The incumbent will lead by example and foster a team environment, ensuring an overall ‘culture of quality’ in the high-quality execution of services provided to clients.

Requirements

• Ph.D. in biotechnology, biotechnology engineering, biochemistry or cell and molecular biology from an accredited institution strongly preferred, with at least 5-7 years of relevant industry, consulting, and/orFDAexperience.
• Alternatively, a master’s degree in related disciplines with at least ten years of relevant experience.

• Prior consulting experience and/or direct FDA or other regulatory interaction strongly preferred.
• Previous experience and strong technical subject matter expertise in the process development, validation and biomanufacturing of biologic drug substance and drug product is strongly preferred.
• Experience with regulatory expectations for biomanufacturing facilities and equipment is a plus.
• Proven ability to lead scientific projects and manage client engagements independently.
• Demonstrated success in business development and sales growth, primarily through existing client relationships.
• Strong technical writing, analytical, and research skills.
• Knowledge of regulatory pathways and strategy development, including familiarity with alternative approaches to regulatory challenges.
• Knowledge of Quality Management Systems and auditing for GMP in the manufacturing and QC environments.
• Knowledge of EMA regulatory pathways and strategy development, including familiarity with alternative approaches to regulatory challenges.
• Effective interpersonal communication and mentoring skills.
• Ability to manage competing priorities in a dynamic, deadline‑driven environment.
• Ability to create effective presentations and leverage current software.

Key Performance Indicators

• Contribution to team revenue and overall business development
• Achievement of individual billable and sales targets
• 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.