Perform all required testing in the chemistry lab for the YBB team, including finished goods, maintenance of lab equipment, and participation in lab projects.
Compensation
The annual base salary range for this position is €30,600.00 - €38,900.00. Total target compensation is determined using objective and gender-neutral criteria, including relevant experience, qualifications, skills, market benchmarks, geographic location, and the scope and responsibilities of the role.
Responsibilities
Perform physical, chemical and particulate testing to support plant functions
Prepare and update control forms, SOIs, and general lab documentation
Prepare trends and technical reports based on data
Maintain cGMP and ISO compliance
Support audit preparations and maintain an audit ready lab environment
Requirements
Degree in Chemistry or science related discipline
Nice to have: 1-3 years experience in a similar role
Nice to have: Good knowledge of analytical principles
Support automation engineering projects by working hands‑on with control systems, programmable logic controllers (PLCs), and manufacturing execution systems across drug substance and drug product manufacturing areas.
Compensation
The salary range for this position is $27.00 - 35.00 USD hourly. All compensation will be determined commensurate with demonstrated experience
Responsibilities
Support automation engineering projects by working hands‑on with control systems, programmable logic controllers (PLCs), and manufacturing execution systems across drug substance and drug product manufacturing areas.
Collaborate with seasoned automation engineers to implement programming changes, system improvements, and troubleshooting for vaccine production equipment in a cGMP environment.
Gain exposure to both upstream (biologics/batch processing) and downstream (formulation, filling, inspection, packaging) automation systems through project‑based assignments.
Participate in data analysis, system documentation, and potential attendance at industry conferences or trade shows to learn about emerging automation technologies
Requirements
Currently pursuing a bachelor’s degree in engineering, computer sciences or related field
Provide engineering support for manufacturing equipment and operations, ensuring process compliance, safety, and continuous improvement in a cGMP environment.
Compensation
This role is exempt and the anticipated compensation for this role is $87,000 - $150,000.
Responsibilities
Plan, coordinate, and execute projects supporting clinical and commercial manufacturing operations
Use historian data to extract and chart process parameters
Analyze process issues and recommend solutions using RCA or other tools
Ensure regulatory compliance of equipment and process performance
Participate in Process Teams to verify process control
Requirements
Bachelor of Science in Chemical, Mechanical Engineering, or related engineering discipline
Produce actinium-225 and other medical isotopes supporting the rapidly growing field of targeted radiopharmaceutical therapies in a cGMP environment.
Compensation
Salary Range: $93,832 - $121,860
Responsibilities
Execute qualified production activities involving chemical preparation and production support, radioisotope processing, and dispensing and packaging operations within a cGMP environment.
Set up and operate production equipment; prepare, identify, control, and reconcile materials, reagents, solutions, consumables, product, and waste.
Maintain clean, organized, and production-ready work areas, equipment, materials, and documentation.
Execute work in accordance with approved procedures, radiological controls, cGMP/Quality requirements, and production schedules while maintaining positive control of the activity.
Produce complete, accurate, and contemporaneous production records and reinforce disciplined procedure use and operational standards.
Requirements
Bachelor's degree in chemistry, chemical or nuclear engineering, radiological sciences, or a related technical discipline
The Sr Manager of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical studies. Actively develops and oversees supply plans to ensure accurate and continuous supply to patients while reducing risk and minimizing waste.
Compensation
Salary Range: $131,800.00 - $176,800.00 annually
Responsibilities
Represent the Clinical Supply Chain on Clinical Study Teams (CST) and provide a high service level to internal stakeholders (e.g. Clinical Operations, Regulatory, Quality, CMC).
Work with Clinical Operations to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines.
Create supply and inventory plans and develop production schedules for clinical trial materials.
Monitor schedule adherence of production schedules and make course corrections if needed.
Manage GMP inventory throughout the supply chain, develop inventory reports, manage upcoming expiry, and ensure drug accountability.
Requirements
Bachelor or Master Degree in Business Administration, Operations Management, or similar education
The role involves performing non-routine complex testing, leading qualification and study directed testing, and ensuring cGMP compliance within a laboratory environment.
Responsibilities
Performs non-routine complex testing, identifies requirements and executes actions as part of change control process
Assists and guides others in the lab with routine testing
Performs high throughput, right-first time work to meet production schedules and project milestones with minimal/no supervision
Leads qualification and study directed testing activities
Reviews and evaluates advanced lab testing results
Requirements
High school Diploma, GED, or equivalent credential
AS degree
BS degree in Microbiology or related scientific field
A senior quality control role focused on performing non-routine complex testing, leading qualification activities, and ensuring compliance within a cGMP environment.
Responsibilities
Performs non-routine complex testing, identifies requirements and executes actions as part of change control process
Assists and guides others in the lab with routine testing
Performs high throughput, right-first time work to meet production schedules and project milestones with minimal/no supervision
Leads qualification and study directed testing activities
Reviews and evaluates advanced lab testing results
Requirements
High school Diploma, GED, or equivalent credential required
AS degree or BS degree in Microbiology or related scientific field preferred
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