PanTera is strengthening its supply chain organization and is looking for an experienced Logistics Coordinator to support the reliable delivery of time-critical, high-value, and regulated shipments. This role is essential to ensuring customer satisfaction and uninterrupted patient access to life-saving therapies.

All outbound shipments will be planned, prepared, and executed end-to-end in close coordination with Production, Quality, and customer delivery schedules. Shipments must comply with strict requirements for temperature control, packaging, security, and timing, in line with regulatory and customer standards.

As Logistics Coordinator, you will act as the central point of contact for freight forwarders, couriers, and customers, managing shipment bookings, documentation, tracking, and escalation of deviations. You will prepare and verify shipping and customs documentation and ensure full traceability within a regulated, GMP-compliant environment.

We are looking for a candidate with a Bachelor’s degree and at least five years of hands-on experience in logistics coordination, preferably in outbound or customer-focused delivery. Certification in Dangerous Goods Transport (such as IATA DGR or ADR) and experience in regulated, hazardous, time-critical, or high-value logistics environments are strong assets, as is prior experience in a GMP manufacturing environment.

PanTera is looking for a talented and experienced laboratory technician to strengthen our R&D team. This is a hands-on and diverse position that requires the willingness to work in a radioactive environment with the focus in assisting in chemical experiments. The ideal candidate has a broad technical skill set, is eager to work in a dynamic and multidisciplinary team at the forefront of medical isotope production. 

In this role, you will support the ongoing production of Actinium-225, with a focus not only on maintenance but also on improving various systems. A significant part of the job involves prototyping and assembly work to support the transition toward a future large-scale Actinium production facility. 

To achieve our mission, we’re looking for a Process Engineer to play a key role in developing the Radon Abatement System, a critical subsystem of the Actinium-225 production chain — from concept to commissioning. You’ll act as PanTera’s in-house Radon expert, leading the design, testing, and validation of the system to ensure safe, reliable, and compliant operation.

You’ll collaborate across disciplines (engineering, safety, quality, and operations) to integrate the system into the broader Actinium-225 production chain. Your work will include experimental validation, risk assessment (FMEA/HAZOP), and supplier follow-up, as well as developing operational and maintenance procedures.

In short, you’ll ensure the Radon Abatement System meets the highest technical, regulatory, and safety standards, while driving its successful delivery from design to deployment.

 

PanTera is launching a new production facility to manufacture large quantities of Ac-225. This facility includes a specialized Quality Control (QC) laboratory responsible for ensuring the quality of Ac-225 produced.

Analysis will be performed to guarantee that the Ac-225 meets specifications to be safely injected into patients. As the product will be used for patients the Ac-225 production and analysis will be performed under current good manufacturing practices (cGMP).

As a Senior QC Lab Analyst, you will work within the QC team under the direct supervision of the QC Manager. Your role will involve supporting the startup of new equipment, developing analytical methods (e.g., ICP-MS, Gamma Spectrometry, and Ac-225 labeling experiments), and contributing to equipment qualification and method validation. Given the cGMP-regulated environment, familiarity with GMP standards is essential.

We seek a candidate with a strong analytical mindset, excellent organizational skills, and a proactive, flexible approach to teamwork. The candidate should be eager to learn new analytical techniques and comfortable working with radioactive materials.

Pantera is starting up a QC lab that will be responsible to examine the quality of the Ac-225 produced. Analysis will be performed to guarantee that the Ac-225 meets specifications to be safely injected into patients. As the product will be used for patients the Ac-225 production and analysis will be performed under current good manufacturing practices (cGMP).

As QC Lab analyst you will be part of the QC team and work under direct supervision of  the QC Manager. You will be responsible for routine analysis of the Ac-225 batches produced by Pantera. You will support the team in development of new analysis methods and validation of the equipment and methods used.

We are looking for a candidate with a strong analytical mindset and a keen sense for organization and structure. As part of a small team proactivity, flexibility and teamwork are key. The candidate is open to lean new analytical techniques and to work with radioactive material.

Some key Responsibilities

• Sample preparation for QC analysis

• Analysis of “in process control” samples and Ac-225 batches produced by Pantera with various techniques such as gamma spectrometry, ICP-MS…

• Report data following standard protocols

• Control of raw materials (incoming goods)

Profile

• Bachelor analytical chemistry or related

• Some experience in similar position is an asset, but not a strict requirement

 

PanTera is looking for an experienced QA associate to join our quality team to support the manufacturing of Actinium-225. 

The ideal candidate will have a strong background in quality assurance within a manufacturing environment, excellent analytical skills, and the ability to communicate effectively with both internal teams and external suppliers. He/she will have a keen eye for detail, and a deep understanding of industry regulations. This role is crucial in ensuring our products meet the highest standards of quality and compliance, thereby maintaining customer satisfaction and regulatory adherence.