Drug Substance CDMO Relationship Manager - Senior Specialist
$83.2k - $101.92kEurofins Agroscience Services North Carolina
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 Drug Substance (DS) CDMO Relationship Manager, you will provide dedicated logistics, scheduling, and meeting-management support for CDMO partnerships for drug substance vendors across late-stage and early-phase programs. Given the criticality of drug substance supply continuity, this role requires a single, embedded External Manufacturing specialist who owns the day-to-day vendor relationship, drives schedule and quality performance, and serves as the primary escalation point for the DS CDMO. This dedicated ownership frees senior leadership to focus on strategic CDMO oversight, technical risk management, and portfolio-wide program delivery.
Key Responsibilities:
DS Vendor Relationship Management
- Serve as the primary point of contact for the DS vendor, owning day-to-day interactions and triaging communications with support and guidance from External Manufacturing leadership.
- Own scheduling and logistics for recurring meetings with the DS vendor (joint technical meetings, JSCs), including calendar coordination across companies and time zones.
- Own batch record / GMP documentation logistics for the DS vendor – tracking review/approval cycle status and driving resolution of bottlenecks.
- Coordinate travel logistics for site visits and workshops with the DS vendor (e.g., FMEA sessions, technical transfer visits), representing EM as needed.
- Maintain the master tracker of DS vendor meeting cadences, deliverables, and deadlines for the EM leadership team.
- Own document routing/version control for DS vendor meeting materials, decks, and governance packages.
- Lead onboarding logistics for any new scope added to the DS vendor engagement (kickoff meeting coordination, distribution list setup, SharePoint/Teams site management).
DS Vendor Performance & Governance
- Assist internal QA organization on Deviation/CAPA tracking administration for the DS vendor – maintaining status trackers, chasing owners for updates, and compiling status for governance reviews (tracking only, not authoring technical content).
- Collaborate with PD/MSAT & QA in pulling recurring technical KPIs and quality performance data for the DS vendor into standard templates ahead of JSCs.
- DS vendor scorecard/dashboard maintenance – updating recurring performance scorecards (OTIF, yield, deviation rates) with vendor-supplied data ahead of JSCs.
- Change control logistics – tracking the DS vendor's change request status (submitted, under review, approved, implemented) and routing signatures.
- Audit and inspection support – logistics coordination (travel, agendas, document requests) for DS vendor audits.
- Provide details to support dashboard updates and internal forums for leadership review.
Qualifications
Minimum Basic Qualifications:
- Bachelor’s degree in science related field with 4+ years of experience or master’s degree in science related field and 2+ years of experience in CDMO/vendor relationship management, program management, or manufacturing operations within pharma/biotech or a related regulated industry.
- Direct experience owning a CDMO or key supplier relationship.
- Experience partnering with PD/MSAT and Quality on technical KPIs, deviations, and change control.
- Strong interpersonal and collaborative/facilitative skills across functions, across internal product leads, and externally as primary point-of-contact with manufacturing partners.
- Proficiency with Microsoft 365 (Outlook, Teams, SharePoint) and/or Smartsheet.
- Excellent written communication for agenda, minutes, and governance reporting.
- Ability to work independently, exercise sound judgment, and proactively manage vendor performance and escalations.
- Attention to detail, highly organized, self-motivated, and ability to find solutions as needed to ensure that project deliverables and timelines are met.
- Understanding of cGMP requirements for pharmaceutical products.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Preferred Qualifications:
- Drug substance manufacturing exposure is strongly 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: $40.00-$49.00 per hour based on education and related industry experience
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Compensation: USD 40 - USD 49 - hourly$40 - $49 per hour
...pharmacology, forensics, CDMO, advanced material sciences... ...Description As Drug Substance (DS) CDMO Relationship Manager, you will provide dedicated... ...External Manufacturing specialist who owns the day-to-day vendor... ...ownership frees senior leadership to focus on strategic...SeniorHourly payFull timeMonday to Friday- Merida Biosciences is seeking a Sr. Manager / Associate Director to lead late-phase drug substance PD/MSAT, interfacing with a CDMO and the CMC team to drive strategy and execution. You will guide process characterization, PPQ development, and regulatory deliverables in...Senior
$135k - $215k
...adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview As a Senior Manager, Drug Substance you will provide oversight of project teams at CDMO’s working on development and production of intermediates and API’s for all stages of clinical...SeniorFull timeContract workWork at office$122k - $174k
...seasoned process chemist who enjoys working on drug substance projects? Do you love working closely... ...this role, you will be responsible for managing the chemical development and external... ...manufacturing activities at global CRO and CDMO partners. You will lead technical...SeniorContract work- Zealand Pharma seeks a Global Head of Drug Substance - Senior Director in Boston to build and lead a new peptide process development function from the ground up, establishing a state‑of‑the‑art lab and team while providing global leadership across Drug Substance. You will...Senior
- ...in Cambridge, MA is seeking a seasoned process chemist to lead drug substance development, scale-up, and external manufacturing... ...programs from late research through clinical trials. You will manage tech transfer to global CRO/CDMOs, design scalable routes, ensure...Senior
- ...Senior Specialist, Drug Safety Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report... ...work independently, playing a critical role in PV Case management to improve case quality, reconcile safety data and diving...SeniorRemote work
$165k - $200k
Description Sr. Manager / Associate Director, Late-Phase Drug Substance PD/MSAT At Merida Biosciences... ...technical interface with our CDMO partner for operations.... ...day-to-day technical relationships with the CDMO partner;... ...: typically for the Senior Manager/Associate Director...SeniorLocal area$117k - $184.2k
...Description We are seeking a Sr. Specialist in Technical Product Management with deep expertise in the analytical method development, drug substance/product process development and manufacturing... ...Management, Stakeholder Relationship Management {+ 2 more} Preferred Skills...SeniorFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$175k - $200k
Senior Manager / Director, Business Development - CDMO $175000 - $200000 per year | San Diego, CA | On-site | Permanent... ...’ll have the freedom to build relationships, develop new business, and grow... ...companies across drug substance and drug product manufacturing....SeniorPermanent employmentFull timeContract work- Title: Senior Scientist, Drug Product Development & External Manufacturing Location... ...of critical drug substance (DS) and drug product (DP) properties... ...stakeholders and external CDMO partners to support process... ...Skills Ability to effectively manage time and prioritize tasks...SeniorLocal area
$122k - $174k
Manager/Senior Manager, Pharmaceutics and Drug Product Cambridge, MA The Opportunity: You will be an integral part... ...compounds You will coordinate with drug substance, DMPK, toxicology and analytical,... .../drug products at CRO's/CDMO's. You will collate, interpret and...SeniorFor contractors- ...Your expertise in analytical techniques and experience in the pharmaceutical industry will be critical for defining strategies and managing projects at contract facilities. A supportive work environment and comprehensive benefits are part of our commitment to your...SeniorContract work
- Moderna’s MTC-S Drug Substance Operations team executes manufacturing of mRNA and LMX/LNP for clinical and commercial vaccines in a GMP environment. The role involves aseptic processing, batch execution, documentation, and use of SAP, LIMS, and CMMS systems. The position...Remote workDay shift
- Moderna is seeking a site-based role in the US for manufacturing of mRNA and LMX/LNP drug substances in a GMP environment. Responsibilities include aseptic processing, filling, and ensuring data integrity and good documentation practices. Role requires HS Diploma and relevant...Shift work
- Moderna in the United States is seeking a Manufacturing Associate I in Drug Substance Operations to help produce mRNA drug substance in a tightly controlled GMP environment. This hands-on role rewards precision, continuous learning, and a team‑driven mindset. You will...
$68.6 - $98 per hour
Drug Safety & Pharmacovigilance Specialist - Onsite, Cambridge MA Primary Responsibilities:Partner... ...and safety physicians to manage and support the authoring... ...with guidance from senior team members and safety physicians... ..., adverse, and negative relationship potentially resulting in...Contract work- Role Senior Manufacturing Associate I in mRNA and LNP drug substance operations, responsible for executing GMP manufacturing processes for clinical and commercial vaccines. Core responsibilities aseptic processing, formulation, filling, dispensing, and documentation compliance...SeniorWork at office
- ...Job Title: Bio/Sterile Drug Product Process Expert Location: Boston, MA – Pier 4 Work Arrangement: Hybrid, onsite 2–3 days/week preferred for local candidates; remote candidates accepted in EST and surrounding states Duration: 1 year, with possible extension up to 2 years...Contract workLocal areaImmediate startRemote work2 days per week3 days per week
- ...You will be an integral part of Relay’s drug product development team supporting Relay... ...production, and process validation. You will manage requisite formulation and process... ...clinical supply. You will partner with drug substance and analytical development functions to define...SeniorImmediate start
- Job Title: Senior Associate Scientist Drug Product Development Location: Cambridge, MA About the Job: This position supports the development of oral... ...supervisor or subject matter experts. Able to plan and manage a set of concurrent experiments. Individual contributor....SeniorTemporary workLocal area
$138k - $184.5k
...Biogen is presently looking to fill a Senior Scientist position within its Parenteral Formulation and Drug Product Development group. The... ...manufacturing robustness, and lifecycle management. Collaborate closely with drug substance, analytical development, device engineering...SeniorTemporary work$230k - $345k
...Development organization and lead drug product process development... ...product presentation. The Senior Director will guide programs... ...validation readiness, and lifecycle management using Quality by Design... ...years of experience in drug substance development and manufacturing...SeniorFull timeSummer workFlexible hours- Relay Therapeutics in Cambridge, MA is seeking a Manager/Senior Manager for Pharmaceutics and Drug Product to lead formulation development for preclinical and early clinical programs. You will design discovery formulations, conduct pre-formulation and stability studies,...Senior
- Relay Therapeutics leads drug product formulation development, overseeing outsourcing at global CRO/CMOs to deliver pediatric‑oriented and commercially viable manufacturing processes. You will drive prototype development and clinical manufacturing activities, while coordinating...Senior
- Biogen is seeking a Senior Scientist to advance parenteral drug product development, leading sterile formulation efforts and technology transfer. You will work across functional teams, drive process validation, and contribute to regulatory submissions in a fast-paced, matrix...Senior
- LifeMine is seeking a Senior Director, Program Management to lead cross-functional project management across our research, preclinical, and clinical-stage drug development programs. This role owns program management for our lead asset LIFE-001 and relevant follow-on assets...Senior
- AbbVie seeks a strategic Discovery Portfolio Manager to oversee portfolio analytics, governance, and executive-level reporting across external... ..., monitor KPIs, and drive continuous improvement in early drug discovery programs. This role emphasizes data-driven decision making...Senior
$175k - $240k
...We’re building a relationship-oriented bank for the modern world. We need talented, passionate professionals who are dedicated... ...CIBC, please visit CIBC.com What You'll Be Doing As a Senior Relationship Manager, you’ll focus on growing direct revenue, retaining high-...SeniorRemote work- 1910 in Boston seeks an experienced computational chemist to lead drug discovery efforts. The ideal candidate will have a Ph.D. and extensive experience in quantum chemical methods and molecular dynamics simulations. This role involves collaboration across interdisciplinary...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Drug Substance CDMO Relationship Manager - Senior Specialist. Be the first to apply!
- university relations manager Boston, MA
- IT business relationship manager Boston, MA
- government relations manager Boston, MA
- labor relations manager Boston, MA
- external relations director Boston, MA
- relationship manager Boston, MA
- wealth management relationship manager Boston, MA
- patient relations manager Boston, MA
- senior relationship manager Boston, MA
- relationship manager corporate banking Boston, MA



