Materials Specialist, Toronto

2 weeks ago

Toronto, Canada POINT Biopharma Full time

POINT Biopharma Global Inc. is a globally focused radiopharmaceutical company building a platform for the clinical development and commercialization of radioligands that fight cancer. POINT aims to transform precision oncology by combining a portfolio of targeted radioligand assets, a seasoned management team, an industry-leading pipeline, in-house manufacturing capabilities, and secured supply for medical isotopes including actinium-225 and lutetium-177. POINT's active clinical trials include FRONTIER, a phase 1 trial for PNT2004, a pan-cancer program targeting fibroblast activation protein-α (FAP-α), and SPLASH, the phase 3 trial for PNT2002 for people with metastatic castration resistant prostate cancer (mCRPC) after second-line hormonal treatment.

TO BE CONSIDERED, APPLICANTS MUST BE LEGALLY ENTITLED TO WORK IN CANADA.

Location: College Street and University Avenue, downtown Toronto. This position requires to be on-site daily.

Reporting to the Manager, Facilities & Logistics at the POINT Institute for Radioligand Innovation (PIRI), the Materials Specialist is responsible for the requisitioning, ordering, inventory management, and disposition of drug product ingredients and single-use components, as well as supplies and spare parts, used in pharmaceutical production and testing at the POINT pharmaceutical GMP manufacturing center.

Overview
- Analyze inventory counts. Purchase materials to ensure that inventory is available to meet production demand.
- Track incoming material to ensure that it arrives on a timely basis. Resolve any issues if there are any delays in transit.
- Ensure that all shipping documents are available for traceability.
- Coordinate and plan routes for shipping. Packaging products. Ensure that product is packaged accurately (as per order and procedure).
- Receiving material and performing basic inspection, verifying accurate quantity (as per order), and forwarding all documents to the relevant departments.
- Organize materials storage area to ensure clear segregation of goods to comply with cGMP requirements.
- Manage inventory following best practices.
- As a Materials Specialist, this individual will also be responsible for the daily oversight of the ERP system, Netsuite, including establishment of system part numbers, barcoding, production planning, and inventory implementation, tracking and reconciliation.
- Assist in establishing and standardizing logistics process. This includes creating SOPs and improving existing SOPs.
- Ensure that the facility is well maintained to meet cGMP requirements. Participate in cleaning activities and ensure that all activities are documented.

Objectives
- To ensure that inventory is always available to support manufacturing and development activities at PIRI site.
- Support Production to ensure drug delivery is on shipped and delivered on time.
- To be able to perform tasks while complying to quality and cGMP requirements.
- To safely work with radioactive materials following ALARA principles and NRC guidelines.
- Ensure all drug product ingredients and materials, as well as all associated supplies, used for the production and testing of drug products are available at the time of production.
- Support Quality Assurance to qualify and manage suppliers of materials used at the POINT manufacturing center.
- Work with technical and quality resources to establish secondary sources of supply for material used at the POINT manufacturing center.
- Participate in the sourcing and cost improvement efforts of the company to drive efficient, reliable, cost effective manufacturing.

Accountabilities
- Help establish logistics and facility process and improve existing process.
- Safely handle and participate in the transfer of radioactive materials throughout the facility.
- Maintaining and reviewing records of inventories, product performance, deliveries, costs and items purchased.
- Requisitioning all materials, supplies, and spare parts needed for drug manufacturing.
- Managing the receipt, quarantine, lot sampling, acceptance, and disposition of material used in drug manufacturing.
- Evaluating suppliers on the basis of meeting defined specifications and other important factors such as quality systems, time to delivery, price and customer service.
- Maintaining drug product on time delivery.
- Analyzing price proposals, financial information, specification sheets, and other information used to determine reasonable pricing.
- Work well in a fast-paced team environment.

**Requirements**:

- High school diploma or GD equivalent required.
- Associates or BS/BA Business, management, purchasing or other appropriate field is considered an asset.
- At least 2 years of relevant experience in a manufacturing environment or similar field of work.
- Materials management experience working in a GMP environment such as pharmaceuticals or medical devices is highly desired.
- Experience working with radiopharmaceuticals will be considered an asset but is not a requ

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