Job Description

Lab Technician, Quality Control

Permanent contract is an option

The position

You are responsible for executing release, stability, and in-process tests, followed by reporting, trending, verification, and approval of raw data.

You plan, conduct, and document routine and non-routine analytical tests as well as non-analytical tasks in line with instructions and established guidelines.

You provide support for deviations and participate in root cause investigations, troubleshooting activities, and investigation testing, along with subsequent follow-up actions. Additionally, you act as a Subject Matter Expert for specific bio-analytical techniques.

You are the Person in Charge (PIC) for lab equipment, Biological Critical Reagent (BCR), managing consumables and chemicals, handling sample shipments and distributions, and fulfilling duties related to EHS and BHV deputies. Furthermore, you perform first-line troubleshooting for testing activities.

Responsibilities

Routine and non-routine release testing, stability testing of late-stage clinical batches, commercial stability batches (Drug Substance) and BCR testing.

Signals problems/improvement opportunities within group/laboratory

Participates in continuous improvement projects and promotes “Lean” behaviors and “Lean” culture

Writes, reviews, and modifies procedures and instructions within own discipline(s)

Assures all QCB activities are performed as per scheduled based on priorities, promoting teamwork and open communication.

Required Education, Experience, and Skills

Bachelor’s degree in science (HLO).

Proven experience in analytical testing (HPLC, TOC, UV, conductivity etc) and bio-analytical testing (ELISA) for at least 3 years.

Extensive knowledge of cGMP and laboratory operation required.

Experience with continuous improvement and Lean principles, such as Lean and Six Sigma tools and techniques.

Good command of the Dutch and English language.

Strong focus on clients.

Team player and flexible.

Living at a reasonable distance of Oss.

At least 32 to 40 hours a week.

Secondary Job Description

Who We Are:

Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions.  Our Vision is clear: A better and healthier every day for every woman.

As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants. 

Search Firm Representatives Please Read Carefully 
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Annualized Salary Range

Annualized Salary Range (Global)

Annualized Salary Range (Canada)

Please Note: Pay ranges are specific to local market and therefore vary from country to country.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites

No Travel Required

Flexible Work Arrangements:

Work Week

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

Number of Openings:

1

Requisition ID:R535144