JobsProject ManagerUnited StatesPROJECT MANAGER

LGM Pharma, LLC

Posted today

PROJECT MANAGER

LGM Pharma, LLC · Franklin Township, New Jersey, United States

Full-timeOn site2-5 yrs$85k–$95kListed as no visa sponsorshipPharmaceutical Manufacturing
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In short

The Project Manager serves as the primary point of contact for clients, managing projects from proposal handoff through final report delivery. They are responsible for coordinating timelines, facilitating communication between scientific teams and customers, and ensuring project milestones are met.

What they're looking for

MUST-HAVE SKILLS

Project ManagementClient RelationsCommunicationTimeline ManagementRisk ManagementData AnalysisMicrosoft OfficeLIMS

ALSO MENTIONED

Project ManagementCommercial OperationsAnalytical ServicesDrug DevelopmentPre-ClinicalClinicalCMCQCPharmaceuticalBiotechnology

Candidates must have a bachelor's degree in business or a related field and 3–5 years of experience in a regulated analytical lab or pharmaceutical setting. Proficiency in Microsoft Office and strong organizational and communication skills are required for this role.

About the employer

LGM Pharma

We Accelerate and Optimize the New Product Pathway from Early Development Through Commercialization.

LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical industry. We secure and optimize your supply chain with our extensive qualified API partner network, global drug product development and manufacturing facilities, and regulatory and market intelligence services delivering customized solutions that get your products to market faster. Full-service, expert support that accelerates the new product pathway. Now that’s smart.

Read more

• Established in 2005 • ISO 9001-2015 QMS certified company • CGMP systems in accordance with ICH Q7 • Main business segments: R&D / Biotech / CDMO / Specialty Pharma Companies, New Drug Delivery Technologies (NDA/505b2) – with heavy concentration on injectables, transdermal, nasal, inhalation, ophthalmic & sublingual drug deliveries Our products originate from our API manufacturing partner sites who are approved by the leading regulatory authorities, such as the US-FDA, EDQM, TGA, UK-MHRA, PMDA etc. LGM’s industry experience enables us to support our clients throughout the entire pathway of drug development, from discovery through commercial production. Based on the scale and scope of development projects with which we are involved, we are able to provide our customers with a seasoned perspective and valuable market insight. LGM Pharma has enhanced its position as a leading supplier of newly approved APIs, including full technical documentation and regulatory support. Our Clients: At LGM Pharma, our clients’ needs are our top priority, and we support our client base consisting of a diverse array of pharma companies, including: • Contract Research, Development & Manufacturing Organizations • Specialty Pharma and Novel Drug Delivery Systems • R&D & Biotech Companies • Generic Pharma Companies • Chemical Catalog Companies • OTC & Private Label Manufacturers • Academic & Government Laboratories • Pharmacy Compounding Industry

INDUSTRY
Pharmaceutical Manufacturing
COMPANY
Privately Held
FOUNDED
2005
HEADQUARTERS
Boca Raton, Florida
SIZE
51-200on LinkedIn
OFFICES
6 on LinkedIn

KNOWN FOR

CDMOAPI SourcingSupply Chain ManagementDrug ManufacturingDrug DevelopmentRegulatory Submission

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Questions about this role

Is this LGM Pharma, LLC role remote?
Tagged on site.
What does it pay?
The posting lists $85,000–$95,000 a year.
Does it sponsor visas?
Listed as no visa sponsorship.
What experience does it ask for?
Listed as 2-5 years.

The posting, in full

JOB TITLE: Project Management DEPARTMENT: Commercial Operations SUPERVISOR: Senior VP, Marketing and Commercial Operations Sannova mission is to help customers bring novel therapeutics and affordable generics to market through the provision of high-quality analytical services that cost-effectively accelerate drug development timelines. Sannova Analytical LLC is a contract research organization focused on providing Pre-Clinical, Clinical, CMC and QC services to the Pharmaceutical and Biotechnology sectors.

▶ READ THE FULL POSTING

JOB TITLE: Project Management

DEPARTMENT: Commercial Operations

SUPERVISOR: Senior VP, Marketing and Commercial Operations

Sannova mission is to help customers bring novel therapeutics and affordable generics to market through the provision of high-quality analytical services that cost-effectively accelerate drug development timelines. Sannova Analytical LLC is a contract research organization focused on providing Pre-Clinical, Clinical, CMC and QC services to the Pharmaceutical and Biotechnology sectors.

GENERAL JOB DESCRIPTION

The Project Manager is the primary day-to-day contact for our customers, owning projects from proposal handoff through final report delivery. You will coordinate timelines, information gathering, project updates and data/report delivery between the lab's scientific teams and customers’ teams.

MAJOR DUTIES AND RESPONSIBILITES

 Serve as the single point of contact for clients; build trusted relationships with sponsors and project teams

 Run kickoff meetings and regular status calls; deliver clear updates on progress, timelines, deviations and risks.

 Track project timelines and milestones, identifying potential roadblocks and implementing solutions to keep projects on schedule.

 Coordinate with cross-functional teams to ensure alignment with project goals and objectives.

 Ensure timely delivery of project outcomes.

 Handle client questions and escalations in a timely manner

 Maintain accurate and up-to-date project records in the LIMS and project tracking tools; liaison with lab directors and customers frequently to keep timelines and status updated

 Keep lab aligned on promised timelines and client priorities.

 Report on on-time delivery, backlog and client satisfaction metrics, and identify opportunities to improve processes.

QUALIFICATIONS FOR THE JOB

 Bachelor's degree in Business, Project management or a related field.

 3–5 years of experience in a regulated analytical lab, CRO, CDMO or pharmaceutical setting, with at least 2 years in project management, client services or a client-facing technical role.

 Proven ability to manage multiple projects, deadlines and stakeholders at once.

 Excellent written and verbal communication; comfortable presenting data and delivering difficult news to clients with clear proactive communication and clear expectations setting

 Strong organizational skills and attention to detail.

 Proficiency with Microsoft Office (Excel, Project, PowerPoint)

 Ability to thrive in a fast-paced work environment and willingness to adapt to changing priorities.

 Ability to problem solve and have sound judgment under pressure.

PREFFERED QUALIFICATIONS

 PMP, CAPM or equivalent project management certification.

 Prior bench experience as an analytical chemist or scientist or prior experience in a life sciences PM role

 Experience with LIMS, CRM systems and project management software such as Monday.com

PHYSICAL REQUIREMENTS

While performing the duties of this job, the employee is required to walk, sit, and use hands to finger, handle or feel tools or controls, reach with hands and arms, balance, stoop, crouch, bend, talk and hear. The employee must lift and/or move up to 20 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, and depth perception. Ability to Travel: <5%.

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This listing comes from LGM Pharma, LLC's own careers site. Apply links go to the employer. Company facts are from LGM Pharma's public profile. Last checked 5 Nov 2026.