Title: Senior Technician, QA, Lab

Requisition ID: 73698

Date: Apr 13, 2026

Location:

Stolberg, NW, DE

Department: Laboratory

Description:

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

In this role you will be part of the global Subject Matter Expert (SME) team for internal testing supporting the development, optimization, and validation of methods for release testing and in-process control. You enjoy hands-on preparatory laboratory work as well as data generation and evaluation using state-of-the-art laboratory equipment. You are highly motivated, reliable, and responsible and ideally well familiar with cGMP conform documentation. You feel comfortable to communicate within an international environment and use these skills to train users and support the global team.

Essential Duties and Responsibilities

Independently execute laboratory studies, qualifications, and validations including protocol non-conformances.
Evaluate and document laboratory results following preapproved protocols in conformance with cGMP requirements.
Contribute hands-on experience to development projects, team discussions and brainstorming sessions.
Collaborate within the global team with respect to global projects.
Support global change control implementations.
Provide training for analysts on global test methods.
Organize and administer consumables, equipment, devices and samples.

Education

Technical assistant (BTA, MTA, PTA, CTA) or laboratory assistant.

Work Experience

Minimum 3 years hands-on laboratory work experience preferably in the relevant experimental areas (bioburden and sterility testing, endotoxin testing, particle testing), if possible, in a cGMP regulated environment.
Experience instrument-based data generation and evaluation

Preferred Knowledge, Skills and Abilities

Excellent English and German verbal and written communication skills
Ability to work independently, with minimal guidance and an attention to detail
Structured, experienced, and precise mode of operation within the laboratory
In-depth experimental skills for selected testing routines
Robust cGMP conform documentation skills
Highly motivated, reliable, and responsible personality
Confident in communicating and presenting within an international, global team
Willing for flexibility with respect to daily routine and working hours, e.g., considering the different time zones the global team is located in
Basic competences in project management
Assured skills in MS-Office and, ideally, in SAP as well as statistical data analysis

Additional Requirements

Job-related activities that require a physical activity such as standing in laboratory environment
Use hands to finger, handle, feel or operate objects, tools or controls and reach with hands and arms.
Job-related activities that require a mental skill or ability such as communication, quick decision making, interpreting data, reading or writing, public speaking, etc. (e.g., Must be able to express or exchange ideas with employees; Must be able to understand direction and adhere to established procedures) #LI-JJ1

Travel Requirements

None: No travel required

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

What We Offer

Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities.

Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives.

Global Career Opportunities: With facilities across North America, Europe, and Asia-Pacific, employees have opportunities for international exposure and cross-functional collaboration.

Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.