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Our client who specializes in the Pharmaceutical industry is looking for a Process Specialist. Your roles and responsibilities will include:
Coordinating scientific and technical Pharmaceutical Technology projects (study, design, evaluate, conclude, implement, control and follow-up) and ensuring that projects are completed in time according to the pre-established time schedule.
Liaising 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.
·Aiding in issuing, checking and approving all Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards
Coordinating with the QC, Production, and Supply Chain departments the manufacturing of the submission/ optimization and validation batches.
Actively assisting and following up on any investigations that might arise during manufacturing and testing of submission, optimization and validation batches.
Assisting in the issuing of manufacturing methods by the requirements defined within the Product Registration Dossiers and filings
Coordinating all aspects of manufacturing process transfers for individual products
Ensuring that all transfer activities are successfully concluded in time for product submission, product launch or any regulatory requirements
Supporting technical and scientific investigations into manufacturing and product-related issues and assisting Production and Quality with troubleshooting related to the formulation, process-related difficulties and validation issues.
Ensuring that appropriate process optimization is carried out when deemed necessary.
Requirements
At least five (5) years of experience in manufacturing or QA of solid oral doses
A good understanding of formulations
Education and Experience
A first degree in a science background or a number of years experience in a manufacturing environment in the Pharma industry or related business
Konnekt: Established in 2007, Konnekt has grown into Malta's leading job agency. Our team is here to simplify your job search by presenting over 400 career options across various fields. We have robust connections with top employers in Malta, making us the ideal choice for anyone considering a career change.
At Konnekt, we believe in straightforward actions and staying true to our values. This commitment has been the driving force behind our success. Whether you're seeking new opportunities or exploring a different career path, we are your reliable partner throughout the process.
Our website provides more insights into our approach and the array of services we offer. Take a moment to explore and discover how Konnekt can be instrumental in shaping your professional journey.
Our client who specializes in the Pharmaceutical industry is looking for a Process Specialist. Your roles and responsibilities will include:
Coordinating scientific and technical Pharmaceutical Technology projects (study, design, evaluate, conclude, implement, control and follow-up) and ensuring that projects are completed in time according to the pre-established time schedule.
Liaising 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.
·Aiding in issuing, checking and approving all Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards
Coordinating with the QC, Production, and Supply Chain departments the manufacturing of the submission/ optimization and validation batches.
Actively assisting and following up on any investigations that might arise during manufacturing and testing of submission, optimization and validation batches.
Assisting in the issuing of manufacturing methods by the requirements defined within the Product Registration Dossiers and filings
Coordinating all aspects of manufacturing process transfers for individual products
Ensuring that all transfer activities are successfully concluded in time for product submission, product launch or any regulatory requirements
Supporting technical and scientific investigations into manufacturing and product-related issues and assisting Production and Quality with troubleshooting related to the formulation, process-related difficulties and validation issues.
Ensuring that appropriate process optimization is carried out when deemed necessary.
Requirements
At least five (5) years of experience in manufacturing or QA of solid oral doses
A good understanding of formulations
Education and Experience
A first degree in a science background or a number of years experience in a manufacturing environment in the Pharma industry or related business
Konnekt: Established in 2007, Konnekt has grown into Malta's leading job agency. Our team is here to simplify your job search by presenting over 400 career options across various fields. We have robust connections with top employers in Malta, making us the ideal choice for anyone considering a career change.
At Konnekt, we believe in straightforward actions and staying true to our values. This commitment has been the driving force behind our success. Whether you're seeking new opportunities or exploring a different career path, we are your reliable partner throughout the process.
Our website provides more insights into our approach and the array of services we offer. Take a moment to explore and discover how Konnekt can be instrumental in shaping your professional journey.