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Senior Technician; Bioanalytics

Job in Jersey City, Hudson County, New Jersey, 07390, USA
Listing for: Ardena Careers
Full Time position
Listed on 2026-08-25
Job specializations:
  • Science
    Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 65000 - 80000 USD Yearly USD 65000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Senior Technician (Bioanalytics)

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.

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
  • 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

Salary Range: $65,000 - $80,000

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Position Requirements
10+ Years work experience
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