More jobs:
Quality Control Expert Technician Incoming goods; m/w/d
Job in
Germany, Pike County, Ohio, USA
Listed on 2026-01-17
Listing for:
Eli Lilly and Company
Full Time
position Listed on 2026-01-17
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst, Quality Control / Manager
Job Description & How to Apply Below
Location: Germany
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.
We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
At Lilly in Germany, we are currently planning and building a high-tech production facility in Alzey (Rhineland-Palatinate), which will expand our production of injectable drugs from 2027 and employ up to 1,000 specialists. To make the most of our innovative production site, we are looking for motivated reinforcements who, together with us, will ensure the supply of Lilly medicines in Germany, Europe, and worldwide, in line with the three Lilly values of "Excellence," "Integrity," and "Respect for People."
** Join our Lilly team in Alzey and start as soon as possible as:
**** Quality Control Expert Technician -- Incoming goods (m/w/d)
**** You need to make sure of:**
* * Timeliness:
* Ensure work is completed in a timely manner to support batch release and site priorities.
* * Safety and GMP Compliance:
* Adhere to Environmental Health and Safety (EHS) requirements and laboratory safety procedures. Maintain cleanliness and contamination control, in alignment with cGMPs, chemical hygiene, and biosafety guidelines.
* * Compliance and Documentation:
* Execute activities in compliance with applicable standard operating procedures (SOPs), methods/protocols, good documentation practices (GDP), and regulatory guidelines.
* * Data Recording and Data Integrity:
* Execute activities in accordance with data integrity standards and ALCOA+ principles.
* * Data Review:
* Perform data review, as assigned, to ensure accuracy and compliance.
* * Deviation Identification and Investigation:
* Identify and escalate any atypical results and potential deviations. Participate in root cause analysis for laboratory investigations and implement corrective/preventive actions, as required. Provide data to support manufacturing investigations, as required.
* * Continuous Improvement:
* Identify and communicate opportunities for improvement.
* * Cross-functional Participation:
* Participate in cross-functional teams (e.g., process team, global working teams, etc.), as required.
* * Training and Mentorship:
* Maintain training competencies and only execute work where qualified. Participate in training and mentorship, as requested.
* * Audit and Inspection Support:
* Execute activities in a compliant manner that supports an ongoing state of inspection readiness. Participate in pre-inspection reviews/checks and provide on-site support during audit/inspections, as requested.
* * Sampling:
* Sample in-coming goods in accordance with the sampling plan. Sampling of in-coming goods may include operations in a biosafety cabinet/laminar airflow in the cleanroom environment.
* * Sample Handling:
* Handle samples in accordance with local procedures to prevent contamination.
* * Sample Collection and Labeling:
* Label samples and document sample collection in accordance with local procedures.
* * Sample Transport:
* Carefully transport samples to the identified area in a timely manner, in accordance with local procedures.
* * Communicate with Warehouse and QA:
* Communicate clearly with Warehouse and QA and work together to ensure samples are collected in accordance with the approved sampling plan.
* * Sample testing:
* Perform testing on incoming goods in accordance with established laboratory procedures and GMP requirements, including but not limited to excipients, printed packaging materials, and so on. Techniques may include Raman, Eye-C, and so on.
* * Equipment usage:
* Perform routine checks and cleaning on equipment in accordance with established methods/procedures. Immediately report equipment malfunctions and coordinate required calibration or maintenance with the QC equipment team.
* * Method Support:
* Support and…
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