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    Eurofins

    Life Sciences

    Project Management Associate

    Louisville, United StatesOn-SiteFull-time1+ yrs experiencePosted 1mo ago
    All Eurofins jobs

    Job description

    The Project Management Associate of Oligo Production is responsible for the oligonucleotide manufacturing operation and implementation of key customer projects to meet production goals, quality, and cost objectives. Perform activities in concordance with FDA-QMS/QSR and ISO-9001 standards; ensure compliance with environmental, health and safety regulations. Select, develop, and evaluates personnel to ensure the efficient operation of the function. Plan and administer procedures and budget, serve as a manufacturing representative and technical expert. This position is full time onsite in Louisville KY, Monday to Friday.

    RESPONSIBILITIES:

    • Leads the teams and manages individual contributors (Supervisor, Team Leads, Production Chemists, Lab Technicians, contractors).
    • Coordinates the activities of project(s) with responsibility for results in terms of timelines, cost, process implementation and employees.
    • Manages Red Folder/ VIP customer list projects
    • Works on problems of diverse scope including multiple projects and/or objectives.
    • Develops and administers schedules and monitors progress (KPI) against objectives. Safety/Quality/TAT/5S
    • Prepares KPI reports and communicate regularly with other managers, upper management, and other designated contacts within the organization.
    • Coaches subordinate(s) on job performance and development.
    • Leads validation activities of new projects and equipment.
    • Leads Kaizen and other improvement projects within department.
    • Ensures BOMs and manufacturing documents are current, effective and maintained properly in electronic document management system.
    • Reviews weekly KPI reports
    • Coordinates weekly safety training and recruitment process within department.
    • Ensures and adheres to GMP compliance and maintain a clean/ traceable work environment.
    • Production Schedule Alignment (Outline deadline requirements for Production, and follow up with schedule to make sure deadlines are met)
    • Point of contact for QC questions regarding RF/VIP projects (reviewing MS/HPLC traces before passing to next production step)
    • Provide updates/ Delays on RF projects (Tracking for RF and VIP projects)
    • Perform activities in concordance with FDA-QMS/QSR and ISO-9001 standards
    • A minimum of a Bachelor’s degree in engineering, chemistry, biochemistry, or similar field.
    • A minimum of 1 years of experience in manufacturing or oligonucleotide field or similar field.
    • Proficiency of organic synthesis and purification techniques.
    • Effective organization and planning skills.
    • Working knowledge of GMP, ISO, and QSR regulations.
    • Experience in documenting and analyzing experimental data
    • Strong computer, scientific, and organization skills
    • Excellent communication (oral and written), and attention to detail

    Schedule:

    • Monday-Friday 8am-5pm

    What we offer:

    • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
    • Life and disability insurance
    • 401(k) with company match
    • Paid vacation and holidays

    Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

    Job details are sourced from the employer's original posting.

    Open job posting
    EU

    About the company

    Eurofins

    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. Eurofins PSS Insourcing has an exciting and rewarding opportunity for a Business Development Manager to join our team.  We are searching for a business development professional with proven experience selling and implementing high-value sales.  Someone who thrives on identifying and closing new business caring for the client through the process will succeed in this role. This position offers the excitement of hunting for new clients with the goal of diversifying our offerings and client base as well as the opportunity to foster and expand partnerships with key clients.  This is a hybrid role working remotely from a home office, travelling locally and within the region for prospect and current client meetings as well as full days spent at current client sites to maximize networking and relationship building opportunities. A successful candidate will have a proven track record and is comfortable reaching out to and meeting with high level decision makers including C-Suite.  This position will manage the strategic sales process including identifying client needs, defining and presenting how PSS can address them, as well as managing the implementation process for new programs. If you’re looking for a rewarding career, a place to call home, apply with us today! 

    View all Eurofins jobs
    Industry
    Life Sciences
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