US Jobs US Jobs     UK Jobs UK Jobs     EU Jobs EU Jobs


Senior Engineer MSAT Bio DP, 2-year limited contract

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Supply Chain Engineering

Job Sub Function:
Process Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Schaffhausen, Switzerland

Job Description:

We are searching for the best talent for Senior Engineer, MSAT Biotherapeutic Drug Product (24 month fixed-term contract)! This hybrid position will be located in Schaffhausen, Switzerland.

As a member of the Site Technical Owner (STO) Team, the Senior MSAT Bio DP Engineer will serve as the Site MSAT representative on multi-functional teams and is responsible for leading the reliability of product processes of commercial product and new product introductions (NPI's) for biologic parenteral liquids, suspensions, and lyophilized products at the Schaffhausen Fill Finish site.

This involves collaborating in multi-functional teams within the site and exchanging knowledge with other locations worldwide.

They will provide technical support and leadership to top-line growth, as well as ensure reliability, compliance, and efficiency of product value chains end-to-end (E2E).

The Site MSAT Rep will also integrate Manufacturing Operations and Pharmaceutical Development, in partnership with Product and Customer Management.
Responsibilities:


* Serve as Site Technical Owner for specific commercial drug products in Life Cycle Management


* Own and coordinate validation activities with internal partners


* Lead or contribute to multi-functional project teams, providing technical guidance and coordinating activities to meet quality, timeline, and compliance objectives


* Implement process capability, quality, and cost improvement changes


* Support E2E technical guidance for product lifecycle activities, including Continued Process Verification (CPV) trending, change implementation, and continuous improvement


* Provide technical feedback and assessments for deviations, investigations, CAPAs, and change controls related to drug product manufacturing processes


* Active participation in internal, customer, and health authority inspections as lead Subject Matter Expert


* Maintain excellent and collaborative relationships with all business p...




Share Job