Hot Pharmaceutical Jobs

Graduate Quality & Regulatory Affairs Coordinator

Graduate Quality & Regulatory Affairs Coordinator This is an excellent opportunity to be working with a dynamic Medical Device company based in Dublin.

Location: Dublin,

Validation Specialist

Validation Specialist Our client is recruiting a Validation Specialist based in the Dublin office and reporting directly to the Operations Manager. The successful candidate will be responsible for the day-to-day administration of Validation Protocols which involves liaising with our Quality, Sales and Service Teams, Technical Support Engineers/ Subject Matter Experts, Suppliers and Customers. Person ·Administration of the Validation System including the development and maintenance of IQ/OQ and PQ/ RQ/ PV protocols. ·Liaise wit...

Location: Dublin,

QA Manager

QA Manager Our client, one of the largest multinational company based in Dublin is recruiting for QA Manager. This is a key position, which involves ownership and accountability for the quality operations activities across the site. This is a challenging, results-oriented position. QA Manager will have involvement in the preparation, support and follow-up of Regulatory Agency inspections including HPRA, TUV Regulatory Agencies, Corporate & Strategic Partners as well as performing internal audits as required. The Position ·To ensure compliance with t...

Location: Dublin,

Senior Manager Product QA

Senior Manager, Product QA Our client, a global biopharmaceutical organisation based in Sligo, are currently recruiting for a Senior Manager, Product QA to join their team on a permanent basis. As Senior Manager you will to lead a technical team of 6 experienced Quality and Regulatory professionals, including 3 QPs. The successful candidate will be responsible for the release of all finished products from the site across API and Drug Product. Responsibilities: • Managing the QP and Regulatory group, including batch release, product performance, new products ...

Location: Sligo,

Quality Assurance and Regulatory Affairs Manager

Quality Assurance and Regulatory Affairs Manager Our client, one of the largest biomedical innovator based in Dublin is looking to recruit QA/RA Manager wh

Location: Dublin North,

Clinical Trial Associate

Our Cork city-based biotech client is kicking off a major new recruitment project which will require the hiring of 100+ in-house Clinical Trials experts over 12 months. A superb office and team environment along with salary and benefits package will reward successful candidates here. Responsibilities The Clinical Trial Team provides clinical trial capabilities in support of clinical development. The Associate is accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and close...

Location: Cork,

Reliability Engineer

In this role, you will provide technical expertise and guidance on Reliability Engineering and Asset Management while driving a culture of continuous improvements and reliability excellence through our MEP programme, and Support Maintenance management to deliver on its objectives. Key Responsibilities: Technical expert / SME on reliability engineering on site. Responsible for reliability standards within the department (equipment, processes, systems and utilities). Responsible for ensuring reliability standards are in line with standards set by the company and i...

Location: Cork,

Mechanical Design Engineer

Mechanical Design Engineer required to focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Engineers are directly involved in the development of innovative products for use in medical procedures. Principal R&D Engineers are directly involved in all stages of the product development process from concept generation through to commercialization of cutting edge devices such as structural heart devices. Responsibilities: Support basic clinical need through opportunity assessment and device concept to prototype. You will participate in...

Location: Galway,

QA Specialist (QC)

This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities at Janssen Biologics as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities.Provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met. GENERAL SCOPE OF RESPONSIBILIT...

Location: Cork,

QA Manager

Our client is a company with a focus on the development and manufacture of generic pharmaceutical products. A key hire has opened up due to expansion. Real opportunities exist with this organization for the right candidate. Some travel is included with role. Previous experience of generics is essential for this post. A superb salary and working environment is on offer. RESPONSIBILITIES 1. Management of QA team a. Supervise all day-to-day activities of Irish QA team b. Recruit new staff as required c. Assign tasks to each QA team member and monitor performance levels. d. Report on reg...

Location: Dublin North,

Validation Engineer

Our client is an innovative start-up in Limerick and seeking a Validation Engineer with experience in software to join their team in a role which is brand-new and reports to the CTO. Responsibilities: • Responsible for the creation of validation documentation including validation plan, validation report, traceability matrix for custom and COTS software • Responsible for the development and execution of manual user acceptance tests • Work closely with business analysts on creation of user requirement specifications meeting regulatory requirements • ...

Location: Limerick,

Quality Assurance Specialist

Reporting to the Quality Director this is a 12 month contract for immediate start. There are excellent opportunities that additional (contract / perm) assignmen

Location: Dublin West,

QA Manager

Our client is a service-provider-of-choice to the pharma and biotech industries in Ireland and internationally. They are seeking an adaptable, skilled and flexi

Location: Meath,

Snr QA Specialist

As this is a role in biotech, it is particularly suitable for pharma experts seeking to break into biopharma. It’s a 12-18month hourly-paid contract, at very attractive rates. The Quality Assurance (QA) Specialist is a senior and active role within the broader QA function. The QA Specialist will typically report to a QA Senior Manager and will be required to be a Subject Matter Expert in their assigned area of responsibility. QA specialists will be required to understand and grasp a broad range of quality related competencies. In addition to routine Quality Assurance ...

Location: Dublin South,