Pharmaceutical Technology Process Specialist

PharOS Ltd in Malta is currently looking to recruit a Pharmaceutical Technology Process Specialist to join their team on a full-time basis.

Overview:
Founded in Athens in 2002, PharOS is a privately owned pharmaceutical Company, developing and supplying generics value-added products with a global portfolio. Our expertise covers all aspects of product development from API sourcing up to market release. We provide a broad portfolio of products and intellectual property to leading pharmaceutical companies.

At PharOS, we have a highly skilled workforce of more than 370 professionals. Biologists, Chemists, Pharmacists, scientists all focused on developing and placing in the market top quality generic and other value-added pharmaceuticals that improve the lives of patients to more than 98 countries. Our people are our core competitive advantage that helps us become one of the fastest-growing pharmaceutical development companies in Europe. For PharOS our customers, are our partners! Our aim is to extend the lifecycle of the product, as our people are able to provide an exceptional level of customer service and support, based on their expertise and professionalism.

Role and Responsibilities:

• To coordinate scientifically and technically Pharmaceutical Technology projects (study, design, evaluate, conclude, implement, control and follow-up) and ensure that projects are completed in time according to the pre-established time schedule
• To liaise with the relevant departments, as necessary, to ensure information is disseminated and coordination of activities across the site is achieved to ensure projects are completed on time
• To aid in issuing, checking and approve of all Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards
• To coordinate with the QC, Production, and Supply Chain departments the manufacturing of the submission/ optimization and validation batches
• To actively assist and follow up on any investigations which might arise during the manufacturing and testing of submission, optimisation and validation batches
• To assist in the issuing of manufacturing methods in accordance with the requirements defined within the Product Registration Dossiers and filings
• To act as the gatekeeper for all incoming information on product transfers
• To coordinate all aspects of manufacturing process transfers for individual products
• To ensure that all transfer activities are successfully concluded in time for product submission, product launch or any regulatory requirements
• To support technical and scientific investigations into manufacturing and product-related issues and to assist Production and Quality with troubleshooting related to formulation, process-related difficulties and validation issues
• To ensure that appropriate process optimization is carried out when deemed necessary.

Experience & Qualification:

• A first degree in a science background or a number of years of experience in a manufacturing environment in the Pharma industry or related business
• At least five (5) years of experience in manufacturing or QA of solid oral doses
• A good understanding of formulations.

PharOS Ltd Offers:

• Competitive remuneration package (including bonus based on performance)
• Private medical scheme
• Continuous training
• Friendly and challenging working environment
• Relocation package.

PharOS is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender identity, gender expression, national origin, or any other basis protected by applicable law, and will not be discriminated against based on disability.