Pharmaceutical Process Development Expert

We are recruiting for an Operations Specialist to support a Pharmaceutical organization in Louth. As part of a team committed to efficiency and teamwork, you will contribute to reduced downtime, increased throughput, and the maintenance of high-quality standards.About the Role:You will provide comprehensive oversight of the OSD filling line setup, operation,...

About the Role:This Pharmaceutical Process Improvement Manager position is an exceptional opportunity for an experienced professional to join a leading pharmaceutical organization in Carlow. The successful candidate will contribute significantly to the company's success, driving improvements in change control processes.Main Responsibilities:Develop and...

We're seeking a highly skilled individual to join our team as a Process Support Specialist. In this role, you will play a critical part in ensuring the smooth operation of our process documentation system and supporting operational activities.Job DescriptionYou will be responsible for managing document systems, generating documentation for operational...

About the Role:We are seeking an experienced Building Automation Expert to join our team in Dublin. As a Pharmaceutical Engineering Specialist, you will play a key role in supporting the development and implementation of our Building Automation System (BAS).Responsibilities:Supporting the BAS: Ensure the smooth operation of the Building Automation System...

Process Engineer - Tech Transfer - Carlow, Ireland - 11 Months ContractDo you want to be involved with exciting pharmaceutical projects?When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are...

We're currently recruiting for an exciting opportunity with a leading Pharmaceutical organization. This position is ideal for individuals looking to join a multinational company renowned for excellence in their industry.Job ResponsibilitiesBe an expert in document systems, including review, approval, and workflow expedition. Create, deliver, and review...

About the RoleThis is an excellent opportunity for a motivated individual to join our team as a Quality Specialist.Responsibilities:Administer event management systems, ensuring compliance with regulatory requirements.Design and approve batch records.Coordinate site change control systems, minimizing disruptions to operations.Develop and implement validation...

About the Role:This is an exciting opportunity to join our team as a Pharmaceutical Maintenance Specialist. You will play a crucial role in maintaining the integrity of our equipment and processes.Responsibilities:Ensure compliance with regulatory requirements and industry standards.Collaborate with cross-functional teams to identify areas for improvement...

Job Description SummaryThe Manufacturing Process Technician reports to the Shift Manager and is responsible for one or more roles relating to the manufacture and inspection of sterile parenteral drugs. Key responsibilities include operating and setting up manufacturing equipment, processing parts and components, performing transactions in electronic systems,...

Quanta Consultancy Services Ltd seeks a skilled Pharmaceutical Project Specialist to join their team. As a specialist in validation engineering, you will play a crucial role in the development and production of veterinary vaccines.The successful candidate will be responsible for designing and executing qualification and validation documentation, as well as...

Quanta Consultancy Services Ltd is seeking a highly skilled GMP Compliance Expert to join their team. As an expert in validation engineering, you will play a critical role in ensuring the development and production of veterinary vaccines meet the highest standards of quality and compliance.Your key responsibilities will include designing and executing...

About the RoleThe Business Manager will be responsible for creating and maintaining a profitable and sustainable Business Unit in the Pharmaceutical ingredients division in Ireland. This involves developing long-term business relationships with Key Customers, identifying and capitalizing on new opportunities to grow the business unit, and promoting the...

Job OverviewThe Manufacturing Process Technician plays a pivotal role in the operation and maintenance of manufacturing equipment at Amgen. This position involves monitoring and adjusting manufacturing processes, troubleshooting any issues, and ensuring the quality of final products. The technician works in compliance with company policies and safety...

Waters Corporation is seeking a Chemical Process Optimisation Specialist to join our Chemistry Consumables team.About UsWe are a global leader in the development, manufacture and supply of high performance liquid chromatography (HPLC), mass spectrometry (MS) and thermal analysis instruments for laboratory, clinical, and industrial applications. Our products...

Company Overview:Quanta Consultancy Services Ltd is a leading provider of consulting services to the pharmaceutical industry. With expertise in quality assurance, regulatory compliance, and project management, we help clients achieve their goals.

Our MissionWe are committed to transforming lives through our science-based approach to medicine. Our mission is to harness the power of biotechnology to deliver high-quality medicines that improve patient outcomes and enhance quality of life.

Company OverviewQuanta Consultancy Services Ltd has established itself as a Centre of Excellence in the pharmaceutical industry, boasting the largest centre for veterinary vaccine development and production worldwide. With over 1000 employees, we continue to push the boundaries of innovation and excellence.The company's commitment to quality and regulatory...

Job OverviewWe are excited to offer a fantastic opportunity for a QC Bioassay Analyst to be involved with critical investment projects both on-site and remotely.ResponsibilitiesWork as directed by the Bioassay Manager/Associate Director, according to Company safety policies, cGMP, and cGLP.Drive compliance with Global policies, procedures, and guidelines,...

Responsibilities: P.O. generation and ordering for manufacturing to support production batches Assist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analyzers and peristaltic pumps....

About the RoleThis is a challenging opportunity for a skilled Process Simulation Technical Engineer to join our team in Carlow. The ideal candidate will have 3-5 years of experience in a sterile manufacturing environment, preferably with Aseptic Process Simulations execution.You will be responsible for designing, authoring, reviewing, approving, and...