Senior Technician (Bioanalytics)

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.

About the role

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 role is described as a practical problem solver with extensive knowledge of Ardena processes.

Responsibilities

• All tasks and responsibilities of a Senior Technician
• Coordination of the execution of a bioanalysis or validation study
• Involvement in training new employees
• Act as System Manager of laboratory equipment
• Perform transfers/method development under supervision of an (Associate) Scientist
• Involvement in the implementation of new equipment

Requirements

• 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

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

Core Competences

• Communicative: Listen before you speak. Engage with others in a way that reflects professionalism, transparency, and respect. Speak out when it matters.
• Accountable: Take responsibility. Be proactive in addressing challenges. Empower each other to make decisions and take ownership.
• Reliable: Commit to delivering on your promises. Act with honesty. Be dependable and supportive.
• Excellent: Approach every task with preparation and focus. Deliver science-led, innovative solutions with attention to detail while keeping the bigger picture in mind. Embrace a mindset of continuous growth.

Benefits

• 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

Pay

$65,000 - $80,000