Logistics & Team Support Specialist - External Manufacturing

Job Description

Job Description

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!

Job Description

As a Logistics Specialist you will provide dedicated logistics support across our CDMO network and float across existing external manufacturing (EM) teams as a flexible resource for general coordination and documentation tasks (such as formatting scorecards and slide decks, capturing meeting minutes, and tracking action items and deliverables) in addition to coordinating meeting scheduling, travel, and documentation flow. This role is designed to free up EM team bandwidth currently spent on coordination, formatting, and administrative execution, allowing teams to focus on strategic CDMO oversight, technical risk management, and program delivery.

Key Responsibilities:

Meeting & Scheduling Support

• Support scheduling and logistics for recurring CDMO meetings (joint technical meetings), including calendar coordination across multiple companies and time zones.
• Support document routing/version control for meeting materials, decks, and governance packages.
• Capture and distribute meeting minutes for ad hoc EM/CDMO meetings.

Reporting & Documentation Formatting

• Format and maintain CDMO/program scorecards and dashboards for EM teams upon request.
• Build and format slide decks and presentation materials for team and governance meetings.

Contract & Budget Administration

• Support EM leads in tracking Statement of Work (SOW) progress and milestone status across CDMO engagements.
• Monitor purchase order (PO) status – issuance, consumption, and remaining balance – and flag discrepancies to EM leads.

Onboarding & Flexible Team Support

• Assist with onboarding logistics for new CDMO engagements (kickoff meeting coordination, distribution list setup, SharePoint/Teams site management).
• Flex across existing EM teams as priorities shift, picking up ad hoc formatting and coordination requests.

Qualifications

Basic Minimum Qualifications:

• Bachelor’s degree in science related field with 1-2 years of experience in project coordination, program management support, or operations within a pharma/biotech, CDMO, or related regulated industry.
• Strong communication and organizational skills; comfortable managing multiple concurrent meeting cadences across external partners.
• Experience supporting cross-functional or cross-company teams.
• Excellent written communication for agenda and meeting minutes preparation.
• Attention to detail, self-motivated, and ability to work independently and anticipate coordination needs proactively.
• Agility to pivot quickly with changing organizational structures and priorities.
• Proficiency with Microsoft 365 (Outlook, Teams, SharePoint) and/or Smartsheet.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications:

• Direct CDMO or manufacturing exposure / experience is preferred.

Additional Information

Position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.

Excellent full-time benefits include:

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Eligibility for yearly goal-based bonus & merit-based increases
• Compensation: $31.50-41.00 per hour based on education and related industry experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.