--- title: 'Consultant I at Syner-G' canonical: 'https://feeny.ai/job/consultant-i-syner-g-boston-massachusetts-asv8d7jf0g22' type: 'job' last_seen: '2026-09-10' --- # Consultant I at Syner-G - **Company:** Syner-G - **Location:** Boston Massachusetts, United States - **Posted:** 2026-08-28 - **Last confirmed live:** 2026-09-10 - **Apply:** https://job-boards.greenhouse.io/synerg/jobs/6163909004 ## Job description ## COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video [here](https://www.youtube.com/watch?v=2rUMvtncuw8). Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. For more information, visit [www.Synergbiopharma.com](https://www.synergbiopharma.com/) ## POSITION OVERVIEW: Syner-G BioPharma Group is seeking a Consultant I to support the planning and execution of drug substance and drug product development programs across a diverse portfolio of client engagements. This client-facing consulting role serves as the operational lead for CMC programs, coordinating cross-functional activities across manufacturing, analytical, quality, regulatory, and supply chain functions from early development through commercialization. The Consultant I is responsible for driving program execution, managing timelines and deliverables, mitigating risks, and ensuring alignment among internal teams, external vendors, and client stakeholders. This role also plays a critical role in clinical supplies management, including forecasting, packaging, labeling, distribution, and inventory planning to ensure successful support of clinical trials. ## WORK LOCATION: Travel to client sites may be required up to 100%, based on project demands and client expectations. ## KEY RESPONSIBILITIES: (This list is not exhaustive and may be supplemented and changed as necessary.) - Develop and manage integrated CMC project plans and timelines across drug substance, drug product, analytical, quality, and regulatory workstreams. - Identify project dependencies, milestones, critical path activities, and resource requirements to ensure successful program execution. - Coordinate end-to-end clinical supplies operations, including demand forecasting, manufacturing scheduling, packaging, labeling, release, distribution planning, and inventory management. - Oversee packaging and labeling activities for investigational products, ensuring compliance with GMP standards, study requirements, and applicable regulatory requirements. - Develop and monitor project budgets, forecasts, and program financials, including vendor invoice review, scope management, and change order administration. - Lead project risk management efforts by identifying, tracking, mitigating, and escalating risks and issues that may impact timelines, quality, or deliverables. - Coordinate cross-functional teams and external partners, including CDMOs, CMOs, laboratories, and specialty service providers. - Facilitate team meetings, governance reviews, and client status meetings, documenting decisions, action items, and project updates. - Prepare and communicate project status reports, dashboards, and milestone reviews for clients and internal stakeholders. - Build and maintain strong client relationships while serving as a trusted project management resource and delivery partner. - Support business development activities through scope definition, proposal support, and identification of opportunities to expand client engagements. ## QUALIFICATIONS AND REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the education, experience, knowledge, skills, and abilities required. Education - Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or a related scientific discipline required. - Advanced degree preferred. Technical Experience - Consultant Level: Minimum of 5 years of project management experience supporting pharmaceutical development or CMC programs. - Senior Consultant Level: Minimum of 8 years of project management experience supporting pharmaceutical development or CMC programs. - Experience managing cross-functional CMC development programs within biotechnology, pharmaceutical, CDMO, or consulting organizations. - Demonstrated experience in clinical supplies management, including supply planning, packaging, labeling, inventory management, and clinical trial distribution. - Experience managing external vendors and development partners, including CDMOs, CMOs, contract laboratories, and logistics providers. - Proficiency with project management tools and software, including Microsoft Project and related planning and reporting applications. - Experience supporting regulatory submissions and health authority interactions is preferred. - Experience working within consulting, fee-for-service, or multi-client environments is preferred. - Experience with commercial supply chain operations, third-party logistics providers, serialization, and distribution activities is preferred. - Exposure to multiple therapeutic modalities, including small molecules, biologics, and advanced therapies, is preferred. - PMP or equivalent project management certification is preferred. Knowledge, Skills & Abilities - Strong understanding of pharmaceutical development and CMC activities across drug substance, drug product, analytical, quality, and regulatory functions. - Knowledge of GMP requirements and clinical packaging and labeling regulations for investigational products. - Strong project planning, scheduling, budget management, risk management, and organizational skills. - Ability to manage multiple projects simultaneously while maintaining high quality and client satisfaction. - Excellent verbal and written communication skills with the ability to effectively engage stakeholders at all organizational levels. - Strong problem-solving, decision-making, and issue-resolution capabilities. - Ability to operate independently in a client-facing consulting environment while effectively collaborating with cross-functional teams. - Demonstrated ability to build trusted relationships and influence outcomes across internal and external stakeholder groups. ## ESSENTIAL FUNCTIONS: Physical Demands: The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required by this position include close vision and the ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment. ## TOTAL REWARDS PROGRAM: We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars. This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous flexible paid time off program, company-paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work “almost anywhere.” However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India. Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time. ## LEGAL STATEMENT: Syner-G is proud to be an Equal Employment Opportunity and Affirmative Action employers. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) are made without regard to the employee’s race, color, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G is an E-Verify employer. ## About Syner-G ## Company Overview - **One-liner**: Syner-G is a strategic development and delivery partner to biopharma innovators, providing integrated scientific, regulatory, technical, and strategic consulting expertise across the drug development lifecycle. - **Entity Type**: Private (Privately Held) - **Headquarters**: Framingham, Massachusetts, United States - **Founded**: Year not publicly specified (operating as Syner-G BioPharma Group following a rebrand from Sequoia Biotech Consulting in 2025) - **Founders**: Not publicly available ## Core Business - **Primary industry**: Pharmaceutical Manufacturing / Life Sciences Consulting - **Target customers**: Biopharma innovators (B2B, Enterprise) — from early-stage drug discovery to commercialization - **Mission/purpose**: To partner with biopharma innovators to turn scientific breakthroughs into real-world therapies faster, smarter, and with greater impact for patients everywhere. ## Products & Services - **Strategy & Transformation Consulting**: Top-tier consulting expertise for M&A integration, AI and digital transformation, and organizational design, helping clients navigate complex change and scale with confidence. - **Scientific, Regulatory & Quality**: Deep scientific, regulatory, and quality expertise to guide therapies through preclinical to commercialization, minimizing risk and streamlining progress. - **Technical Operations & Delivery Infrastructure**: Hands-on technical expertise and operational leadership embedded alongside client teams to manage technical operations and infrastructure, turning strategy into scalable, compliant execution. ## Market Standing - **Valuation**: Not disclosed (Private company) - **Key Metric**: Total Funding — Venture Round raised on 2020-10-01 (1 investor); also acquired RMC Pharmaceutical Solutions (2023-01-19) - **Notable Investors/Partners**: Not publicly disclosed (single investor in venture round); clients include top biopharma firms (Thermo Fisher Scientific, Johnson & Johnson, Pfizer, Vertex Pharmaceuticals, GSK, etc. as talent sources) - **Growth Signals**: - Headcount: 266 employees (+47.4% YoY, +111 people) - LinkedIn followers: 12,184 (+34.9% YoY) - Active job postings: 21 (+425% YoY) - Rebranded from Sequoia Biotech Consulting to Syner-G BioPharma Group in June 2025 - Appointed Scott Bergeron as Chief Commercial Officer in April 2025 - Global presence: North America (US, Canada), Europe (Germany), APAC (India) — 400+ professionals - Won "Best Places to Work" by BioSpace for 2024, 2025, and 2026 (third consecutive year) - Multiple workplace awards: Gold Bell Seal for Workplace Mental Health (2026), Healthiest Employers (California, Colorado), Mployer Top Employee Benefits (2024, 2025) ## Competitive Advantages - **Integrated expertise**: Combines scientific, regulatory, technical, and strategic consulting under one roof — a rare "Strategic Development & Delivery Partner" model. - **End-to-end lifecycle support**: From preclinical through commercialization, reducing risk and accelerating timelines for biopharma clients. - **Deep talent pool**: 400+ professionals globally with strong recruiting from top pharma (Thermo Fisher, Pfizer, Vertex, GSK) and a consulting DNA (many hires from Sequoia Biotech Consulting). - **Award-winning culture**: Consistently recognized as a top workplace, signaling strong employee satisfaction and retention. ## Strategic Focus - **Growth & expansion**: Rapid headcount growth (+47% YoY), global footprint expansion (India, Canada, Germany), and active hiring across all functions. - **Digital & AI transformation**: Explicit focus on AI and digital transformation consulting as a core service line. - **M&A integration**: Helping clients navigate complex M&A — and demonstrating capability through own acquisition of RMC Pharmaceutical Solutions. - **Commercial leadership**: Recent appointment of CCO signals aggressive go-to-market and commercial scaling. ## Why Work Here - **Meaningful work**: Directly contribute to advancing breakthrough therapies that improve patient lives. - **Award-winning culture**: Recognized as a "Best Place to Work" by BioSpace for three consecutive years (2024–2026), plus awards for mental health, wellness, and benefits. - **Remote-first work**: Remote-first policy with summer flexibility, home office setup allowance, and flexible time off. - **Comprehensive benefits**: Medical, dental, vision, 401k with corporate matching, paid parental leave, employee assistance program, pet insurance, fitness reimbursement, discount marketplace, and more. - **Growth opportunities**: Rapidly growing company (+47% YoY headcount) with varied, thought-provoking work across diverse clients and projects. - **Bonus eligibility for all positions** — all employees share in success. - **On-site childcare at HQ** (Framingham, MA). - **Values-driven culture**: Emphasizes curiosity, collaboration, integrity, empowerment, and continuous learning. ## Sources 1. [synergbiopharma.com](https://synergbiopharma.com/) 2. [synergbiopharma.com/careers](https://synergbiopharma.com/careers/) 3. [Greenhouse Job Board](https://job-boards.greenhouse.io/synerg) 4. 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