d) at Eli Lilly and Company

Alzey, Rhineland-Palatinate, Germany

Apply Now

Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

PharmaceuticalsIndustries

Requirements

(Not explicitly listed in the job description; focus is on responsibilities and role fit for motivated individuals with relevant experience in quality assurance, GMP, and parenteral production.)

Responsibilities

Ensure a safe working environment and safe working practices; support all health, safety, and environmental goals of the company and site
Act as the main point of contact for internal/external customers and answer general information requests in your area of expertise
Train and coach operations and support personnel on quality issues
Support production activities on-site with regular presence in the assigned production area
Follow good documentation practices and adhere to site procedures
Capture, review, maintain, and approve GMP information/data in the appropriate systems and within specified deadlines (e.g., electronic batch documents, logbooks, etc.)
Design, revise, and archive standard operating procedures as well as associated forms and training materials in your area of expertise
Support the resolution of equipment alarms and other issues in quality systems such as Veeva and MES
Make initial decisions on deviations in production areas and escalate as needed
Support batch release and participate in deviation investigations
Create, review, and approve GMP documents; review batch documentation
Ensure compliance with GMP requirements through on-site quality monitoring in key areas: material/equipment preparation, formulation and aseptic filling, visual inspection

Skills

Key technologies and capabilities for this role

Quality AssuranceParenteral ManufacturingGMPFacility QualificationPharmaceutical ProductionAseptic ProcessingValidation

Questions & Answers

Common questions about this position

What is the work location for this Quality Assurance Technician role?

The position is based at the new high-tech production site in Alzey, Rheinland-Pfalz, Germany, where you will support on-site quality monitoring during production shifts.

What are the main responsibilities of the Quality Assurance Technician?

You will support qualification of the new production site, perform on-site quality monitoring in areas like material preparation, aseptic filling, and visual inspection, handle deviations, support batch release, ensure GMP compliance, and create/review GMP documents.

What company values guide the work at Eli Lilly?

Eli Lilly operates under the three values of 'Exzellenz' (Excellence), 'Integrität' (Integrity), and 'Respekt für Menschen' (Respect for People), emphasizing teamwork and putting people first.

Is this a remote or on-site position?

This is an on-site role requiring presence during production shifts at the Alzey facility to support quality monitoring and production activities directly.

What makes a strong candidate for this Quality Assurance Technician position?

Ideal candidates are highly motivated, show team spirit, work cross-functionally, and are eager to contribute to building a new production site while ensuring GMP compliance and quality standards.

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters

1876Year Founded

$1,180.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.

Potential construction delays in Indiana could affect GLP-1 drug production timelines.

Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.

Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.

FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.

Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.

Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

Land your dream remote job 3x faster with AI

Try Jobo Free