Optometrist - Cork Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements. Full-Time or Part-Time | Independent Opticians | €65,000 to €85,000 | 45 Minute Tests Please note the employer is unable to offer visa sponsorship for this position. Applicants must already have full eligibility to work in Ireland Zest Optical Recruitment is working with a long-established independent Opticians in central Cork to recruit an Optometrist on either a full time or part time basis. This is a well regarded, family run practice with a strong reputation across the Munster area. Patients are offered a wide choice of frames, from budget to designer, and the team is known for taking time to deliver thorough, friendly care. Optometrist - Role Highlights Join a long-established independent Opticians with an excellent local reputation Central Cork city location with a loyal, mixed patient base 45 minute testing to allow you to deliver consistent, high quality care Modern, well equipped testing rooms and a supportive clinical team Mix of full eye examinations, contact lens work and aftercare Full time or part time options:Full time, 5 days per week, or Part time covering 3 of 4 days from Monday, Thursday, Friday and Saturday Working hours 9.00am to 5.30pm with a 1 hour lunch break Salary in the region of €65,000 to €80,000, depending on experience, with flexibility for the right personBenefits Supportive, close-knit team environment Ongoing CPD and clinical development encouraged Professional fees covered Staff discount on frames and lenses Additional benefits discussed at interviewOptometrist - Requirements Fully qualified Optometrist registered (or eligible to register) with CORU Comfortable working in an independent setting, focused on patient care rather than volume Strong communicator who enjoys working as part of a small team Friendly, professional and able to build long term patient relationshipsWhy Apply? If you are looking for an Optometrist role in Cork that offers real clinical time with patients, a supportive independent environment and a strong salary package, this is an excellent opportunity. You will work with longer appointment times, a varied patient base and a team that values quality over quantity. xsokbrc Apply Now To be considered, please send your CV to Rebecca Wood at Zest Optical using the Apply link. If you would like to discuss the role first, call (phone number removed)

Competitive Salary & Company Benefits | Dublin, Ireland Any additional information you require for this job can be found in the below text Make sure to read thoroughly, then apply. Monday to Friday, 9.00am - 5.00pm (potential for flexibility on start/end times based on 7.5hrs/day) Are you looking to work for a rapidly growing UK Pharmaceutical company, who are passionate about improving patients’ lives across the world? Aspire Pharma is an asset-light pharmaceutical manufacturer. It licenses and develops niche pharmaceutical products that offer innovative formulations, value for money for payors, and reliable supply arrangements in markets which are often underserved. The business has a highly diversified portfolio of more than 250 products across a number of categories, including branded specialty products and unbranded niche generics in therapeutic areas such as urology, ophthalmology, CNS and dermatology. Do you want to be part of the journey? If so, here is your chance! The Role To provide full administrative support for the Quality Control and Assurance activities of the company in relation to QMS Compliance. What will you be doing? As a QMS Compliance Executive, you will be responsible for the maintenance of, and compliance with, the Aspire Pharma Limited Group’s Irish/EU and UK QMS, where Irish/EU and UK GXP covers all UK and EU GXP guidelines referenced in APL’s Quality Site Master File/Quality Manual, including: staff training; documentation control; change control; non-conformance/deviations; validation; corrective and/or preventive actions; regulatory intelligence; internal audits; self-inspections; management review; monthly checks; licence variations; and launch activities for area. You will also get involved in Operational Compliance activities, such as release of product and credentials (Bona Fides), as and when required. The Person * Written and spoken English with good communication Skills * Time management skills * Good attention to detail * Proactive team player * Proficient in MS Office (including, word, excel and outlook) * Proficient in Q Pulse or other electronic QMS (desirable) Experience and Education: * Science graduate * Experience not essential (1-3 years desirable) Why join us? * As well as a fantastic, inclusive company culture, where employees are truly valued and a competitive salary, we also offer an ever-improving benefits scheme to support your physical and mental well-being which include: * Generous Pension Scheme. * Life Assurance cover and Employee Assistance Program. * 23 days’ holiday plus Bank Holidays. xsokbrc * Learning and Development opportunities. * Excellent opportunities for progression

Competitive Salary & Company Benefits | Dublin, Ireland Any additional information you require for this job can be found in the below text Make sure to read thoroughly, then apply. Monday to Friday, 9.00am - 5.00pm (potential for flexibility on start/end times based on 7.5hrs/day) Are you looking to work for a rapidly growing UK Pharmaceutical company, who are passionate about improving patients’ lives across the world? Aspire Pharma is an asset-light pharmaceutical manufacturer. It licenses and develops niche pharmaceutical products that offer innovative formulations, value for money for payors, and reliable supply arrangements in markets which are often underserved. The business has a highly diversified portfolio of more than 250 products across a number of categories, including branded specialty products and unbranded niche generics in therapeutic areas such as urology, ophthalmology, CNS and dermatology. Do you want to be part of the journey? If so, here is your chance! The Role To provide full administrative support for the Quality Control and Assurance activities of the company in relation to QMS Compliance. What will you be doing? As a QMS Compliance Executive, you will be responsible for the maintenance of, and compliance with, the Aspire Pharma Limited Group’s Irish/EU and UK QMS, where Irish/EU and UK GXP covers all UK and EU GXP guidelines referenced in APL’s Quality Site Master File/Quality Manual, including: staff training; documentation control; change control; non-conformance/deviations; validation; corrective and/or preventive actions; regulatory intelligence; internal audits; self-inspections; management review; monthly checks; licence variations; and launch activities for area. You will also get involved in Operational Compliance activities, such as release of product and credentials (Bona Fides), as and when required. The Person * Written and spoken English with good communication Skills * Time management skills * Good attention to detail * Proactive team player * Proficient in MS Office (including, word, excel and outlook) * Proficient in Q Pulse or other electronic QMS (desirable) Experience and Education: * Science graduate * Experience not essential (1-3 years desirable) Why join us? * As well as a fantastic, inclusive company culture, where employees are truly valued and a competitive salary, we also offer an ever-improving benefits scheme to support your physical and mental well-being which include: * Generous Pension Scheme. * Life Assurance cover and Employee Assistance Program. * 23 days’ holiday plus Bank Holidays. xsokbrc * Learning and Development opportunities. * Excellent opportunities for progression

Optometrist - Cork, Ireland Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today. Full-Time | 45-Minute Testing Times | Support for Further Qualifications Salary up to €85k. We're seeking a friendly and clinically focused Optometrist to join our welcoming independent practice in Cork, Ireland. This is an excellent opportunity to work in a patient-centred environment where quality care always comes first. What We Offer 45-minute testing times - giving you the space to deliver thorough, personalised eye care Predominantly Monday to Friday, with every other Saturday required Ongoing support for professional development and additional qualifications A warm, close-knit team in a modern, well-equipped practice Strong emphasis on clinical excellence and continuity of careAbout You Qualified Optometrist Committed to providing exceptional patient experiences Confident, approachable, xsokbrc and keen to build lasting relationships within the community Enthusiastic about further learning and clinical growthIf you're looking for a role that offers professional freedom, work-life balance, and a supportive environment to grow your career, we'd love to hear from you. @INDALEX

Evolve is proud to be partnering with a market-leading healthcare organisation to recruit an ambitious Graduate Medical Sales Representative. This is a rare and exciting chance for a motivated Science Graduate to kick-start a rewarding career in medical sales – one of the most dynamic and high-growth sectors in healthcare. Scroll down for a complete overview of what this job will require Are you the right candidate for this opportunity In this role, you won’t just be selling products – you’ll be making a real impact. You’ll take ownership of promoting and driving sales of a cutting-edge portfolio of IV and Oncology treatments across leading hospitals in the Republic of Ireland You’ll work closely with healthcare professionals, building strong relationships and providing valuable product knowledge to support patient outcomes while contributing to the company’s regional and national sales success. What’s on offer: Excellent Salary & Benefits - Competitive starting salary along with bonus, car or car allowance, private healthcare, pension and more! Direct Leadership Access - Interview and work closely with a hiring manager who is an experienced leader, passionate about patient impact, and committed to mentoring you to succeed. Career Growth & Development – Access structured training, certifications, and mentorship from industry leaders. Make a Real Impact - Contribute to life-changing IV and Oncology products that directly improve patient lives. Ideal Requirement for the Graduate Medical Sales Representative * Mobility matters – a full UK driving licence is essential, giving you the freedom to manage your territory and meet customers face-to-face. * Launch your career in medical sales – ideal for recent graduates with a scientific background who are eager to apply their knowledge in a dynamic, commercial environment. * Bring your sales flair – previous experience in a customer-facing sales role will set you up for success, giving you the confidence to engage and influence healthcare professionals. * Stand out from the crowd – if you’ve researched the medical sales industry or gained shadowing experience with a Medical Sales Representative, you’ll have a real edge. * Turn ambition into action – above all, we’re looking for individuals with a strong desire to break into medical sales and build a rewarding long-term career. Role Responsibilities for the Graduate Medical Sales Representative * Shape winning strategies – collaborate with the management team to design and deliver successful sales and marketing plans that unlock growth in key accounts. * Work cross-functionally – liaise with colleagues across departments to ensure business objectives are not only met but exceeded. * Drive expansion in Ireland – work with the Sales Manager to launch and grow exciting new business streams, playing a pivotal role in strengthening the company’s footprint in the Irish market. * Stay ahead of the curve – maintain in-depth knowledge of your customers, accounts, and services, while keeping up to date with marketplace changes and the latest clinical developments. Recruitment Process 2/3 stage interview process. Connect with a hiring manager and team who are committed to guiding your career and helping you make an impact. Interested? Please click apply, or contact Andy Boyd for more details Evolve is a leading recruitment and outsourcing organisation, operating within the Pharmaceutical, Healthcare, Medical Device and Life Science sectors. xsokbrc Equal opportunities are important to us. We believe that diversity and inclusion are critical to our success as a company. We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristics

If you are a current Jazz employee please apply via the Internal Career site. Find out exactly what skills, experience, and qualifications you will need to succeed in this role before applying below. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit more information. Brief Description: The Manager, Clinical and Pharmacovigilance Quality Assurance for Pharmacovigilance (PV) system is a significant contributor to Global Quality and is responsible for coordinating activities to regularly verify that Jazz PV system Vendors, commercial partners and Jazz Global R&D/Quality and other teams are operating in line applicable regulations, industry standards, Jazz policies, procedures, and quality standards in support of the Quality Management System & PV system. In addition, the Manager will support Global Quality/ R&D leaders in providing strategic input and tactical implementation for pharmacovigilance system activities and projects, identify and communicate compliance risks, oversee action plans to mitigate risks (if applicable), and be actively involved in inspections and inspection-readiness activities. This person will participate in interdepartmental teams meetings and at times may be asked to perform activities to support other GxP areas, quality operations, and global quality systems. Essential Functions Gain and maintain professional expertise and knowledge of local and international regulations relative to pharmacovigilance system and quality Contribute to the execution of Global PV system audit strategy, and implementation within the Quality Management System Perform reviews on internal and external SOPs; participate in the development of SOPs for Quality or PV System stakeholders Support updates of the quality related sections in the Pharmacovigilance System Master File (PSMF) or similar documents Perform execute and evaluate PV-System auditee risk assessments Coordinate and implement strategic audit plans for pharmacovigilance system activities that include service providers, vendors, business partner, and internal audits. For pharmacovigilance system audits conducted directly by Jazz personnel or conducted by a vendor on behalf of Jazz (external audits) participate as auditor/co-auditor and/or manage the relationship with the vendor. Present QA findings/observations to in-house staff and, if appropriate, to the responsible service provider, vendor, or partner company. Contribute to the evaluation of corrective and preventative action (CAPA) findings to identify quality-related signals and trends for improvement; ensure adequate and timely closure of CAPAs generated from audits. Participate in inspection readiness and inspections as assigned. May perform one or more inspection roles during an inspection (e.g. inspection readiness training, runner, scribe, backroom lead, SME preparation, QA checks, etc.) Identify and escalate critical quality issues to senior Quality management Contribute to the development of continuous quality process improvements and the identification of identifying root causes for investigations and effectiveness checks if appropriate Represent CPVQA within interdepartmental teams / project groups and innovation projects Maintain current training in accordance with the training curriculum This position may require up to 30% travel Required Knowledge, Skills, and Abilities Established Pharmacovigilance or Quality professional Strong GVP knowledge & expertise Excellent written and verbal communications skills Ability to work in an entrepreneurial and fast-paced culture. GVP auditing experience is preferred. GVP lead auditor certification is desirable. Self-directed and ability to take action as needed with oversight. Ability to collaborate and partner with various internal and external business partners Ability to work in a team environment. Disciplined, detail orientated, and strong time management skills Knowledge of post-authorization commitment requirements is preferred (Phase IV, PASS Studies) and Managed Access Programs (PSPs/MRPs, Early access etc.) is desirable. Knowledge and experience with GCP, GLP, and GDP is a plus. Inspection experience with FDA, MHRA (or other EU Competent Authorities); experience with emerging markets Regulatory Authority such as PMDA a plus. Required/Preferred Education and Licenses Bachelor’s degree in a related field is required; Master’s degree in management, leadership or scientific discipline a plus. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. xsokbrc For more information on our Benefits offerings please click here: working/work at home options are available for this role.