Thermo Fisher Scientific Pharmaceutical Jobs in Johannesburg
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Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them.
Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon
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Job Responsibilities
- Provide support to Clinical Research Products Management Center (CRPMC) and NIAID/Division of AIDS) in storage and distribution of clinical trial research products in accordance with Good Pharmacy Practice, Good Distribution Practice and Good Manufacturing Practice. To achieve this Task, you will assist and support the Southern Trials ICRPMC Pharmacists and Team in the following responsibilities:
- Review, monitor and process protocol-related clinical site orders, from receiving the order through to delivery:
- Monitoring orders in COSMOS and from email communications, processing in COSMOS and Manually: Reviewing, verifying, checking and approving orders. Verify correct choice of samples from inventory for each order.
- Working and communicating with the Technicians on processing the orders and check pulled orders against paperwork and COSMOS.
- Interface and interact with customers: USA CRPMC, USA Division of AIDS (PAB) and clinical trial site Pharmacists on all matters related to study product orders and shipments (by telephone and email communication).
- Prepare paperwork for International Sites and send it to the Sites and the Couriers for import permit and approval to ship. Process approved orders and check orders against paperwork after being pulled by Technicians.
- Assist with preparation, reviewing, revision and updating of controlled documents when requested (SOPs, Forms and SWIs).
- Assist with Trial Master File (TMF) filing of shipment documents and the physical archiving of shipping documents for all the protocols.
- Assist with keeping the Site Address File for Shipments updated.
- Assist with handling customer queries (e.g. on clinical site orders, Quality Assurance and Complaints) when requested.
- Assist in supervision and monitoring of good housekeeping, environmental monitoring and control, cold chain maintenance in the warehouse and storage equipment.
- Assist to supervise and participate in periodic stock counts and destruction of obsolete study products.
- Assist to prepare batch record for Auxiliary Labeling of study products with protocol number and perform QC checks.
- Assist with any other special requests / assignments made by RP or Pharmacists that may be necessary.
- Undergo all required training, including USA-based training, online and practical training in order to perform your duties as expected. Record the training performed.
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