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Ardena

Senior Technician (Bioanalytics)

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What they do

A Laboratory Technician performs routine tests on samples of body fluids, tissues, and other substances for diagnostic and research purposes. Works under the supervision of a medical laboratory technologist in a laboratory or healthcare facility.

$51,740 / year median in New Jersey

+1% projected growth

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Job Description

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BIOANALYTICAL LABORATORY
    SOMERSET
    (NEW
    JERSEY, US
    )
    • ONSITE Senior Technician (Bioanalytics) We usually respond within a week About Ardena Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development.
    Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market. The Ardena Group operates from five sites across Europe and the United States, employing more than 750 professionals. Ardena European sites are located in Oss and Assen (the Netherlands), Ghent (Belgium), and Pamplona (Spain). Ardena US facility is based in Somerset, New Jersey. For the Ardena Business Unit based in Somerset (US), we are looking for a Senior Technician (Bioanalytics) Ardena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support. Job Overview
    Position:
    Senior Technician
    Department:
    Bioanalytics
    Location:
    Somerset (US) The Senior Technician performs all tasks focused on bioanalysis and validation studies. The Senior technician is able to independently execute their tasks and is involved in coordinating and coaching technicians. The Senior technician is described as a practical problem solver and has extensive knowledge of Ardena processes. Key Responsibilities All Tasks and Responsibilities of a Senior Technician
    • Coordination of the execution of a bioanalysis or validation study
    • Involved in training new employees
    • Can be a System Manager of laboratory equipment
    • Performs transfers/method development under supervision of an (Associate) Scientist
    • Can be involved in the implementation of new equipment
    JOB FACTORS
    (Knowledge, ABILITES, SKIlLLS)
    • Demonstrates a good understanding of validation principles and bioanalytical workflows.
    • Developing moderate capability to explain complex concepts and share knowledge effectively.
    • Quickly adjusts to changing priorities, new technologies, and evolving project requirements.
    • Shows strong ownership of tasks and projects, ensuring compliance and reliability.
    • Provides guidance and support to colleagues.
    • Capable of organizing activities to meet project goals.
    • Maintains high standards in all deliverables, with strong attention to detail and compliance.
    • Able to identify and resolve issues within bioanalytical and validation processes.
    • Developing problem-solving skills specific to method development challenges under supervision.
    • Effectively prioritizes tasks and meets deadlines under pressure.
    Core Competences C Communicative Listen before you speak. Engage with others in a way that reflects professionalism, transparency and respect. Speak out when it matters. A Accountable Take responsibility. Be proactive in addressing challenges. Empower each other to make decisions and take ownership. R Reliable Commit to delivering on your promises. Act with honesty. Be dependable and supportive. E Excellent Approach every task with preparation and focus. Delivery science-led, innovative solutions with attention to details while keeping the bigger picture in mind. Embrace a mindset of continuous growth.
    EDUCATION & EXPERIENCE
    Required qualifications
    • : Preferred qualifications:
    • Medium or high professional level of laboratory related education (MBO/HBO) 1-3 years of relevant experience in a regulated environment (GLP/GxP preferred)
    • Fluent in English (verbal and written); Dutch is a plus.
    • Proficiency in Microsoft Office tools (Word, Excel, Outlook)
    • Or an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job/role.
    What Ardena Offers Ardena is a science-driven and people-focused employer. Working at Ardena means contributing to pharmaceutical projects that support the availability, safety, and quality of medicines for patients worldwide. Ardena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers across functions and locations. Benefits and perks at Ardena include:
    • Competitive salary and tailored benefits package (adjusted per role and location)
    • Flexible working arrangements (where applicable, depending on role and site)
    • Access to professional development and training programs
    • Meaningful work on pharmaceutical development projects that advance patient health
    • A values-driven culture guided by Ardena's CARE principles: Communicative, Accountable, Reliable, and Excellent How to Apply Ready to advance your career in pharmaceutical development?
    through the Ardena Careers website at careers.ardena.com.
    Salary Range:
    $65,000 - $80,000 Department Bioanalytical Laboratory Locations Somerset (New Jersey, US)