Quality Control Specialist Join our dynamic team as a Quality Control Specialist and play a vital role in ensuring the highest standards of quality in a fast-paced pharmaceutical environment. This full-time on-site position offers an exciting opportunity to contribute to the release of critical products, support continuous improvement initiatives, and uphold compliance with stringent regulatory and quality guidelines. If you’re passionate about quality assurance and want to work in a collaborative setting, this is the perfect role for you. Your Role and Responsibilities As a Quality Control Specialist, you’ll be responsible for the release of incoming goods, outsourced production and packaging products, as well as internal processes, ensuring full adherence to quality procedures, legal directives, and market authorizations. Your expertise will help drive quality improvements, communicate supplier requirements effectively, and maintain impeccable documentation practices. Support and guidance will be provided as you ensure product and process quality meets the highest standards. Required Skills Excellent communication and organizational abilities Solid understanding of quality assurance processes in a pharma setting Knowledge of documentation and record-keeping best practices Ability to interpret and apply quality and legal guidelines Strong attention to detail and problem-solving skills Nice to Have Skills Experience with quality systems and regulatory compliance in pharmaceuticals Familiarity with electronic documentation systems Previous experience in a similar role within a GMP environment Preferred Education and Experience Degree or diploma in life sciences, pharmacy, or related field Prior experience working in pharmaceutical quality control or assurance (minimum 1-2 years preferred) #J-18808-Ljbffr
Planet Pharma Group is seeking a Quality Control Specialist in Leinster, Ireland. This full-time onsite role involves ensuring product quality by overseeing the release of goods and compliance with regulations. The successful candidate will possess strong quality control skills and attention to detail. Education in Quality Assurance or related fields is preferred, alongside relevant experience in a manufacturing or pharma setting. This position supports variable shifts to enhance work engagement. #J-18808-Ljbffr
Join Our Team as a Quality Control Specialist Are you detail-oriented with a passion for ensuring top-tier product quality? We are seeking a dedicated Quality Control Specialist to play a vital role in maintaining the highest standards at our facility. This full-time onsite position offers an exciting opportunity to work within a dynamic environment, contributing directly to product excellence and compliance. In this role, you will be responsible for the release of incoming goods, outsourced production batches, and process products, ensuring strict adherence to quality, legal, and market guidelines. You will advise on and implement quality improvements, communicate requirements effectively to suppliers, and maintain meticulous documentation practices–all supported by a collaborative team environment. The position involves shift work, including day and night cycles, providing a varied and engaging work schedule. Required Skills: Strong understanding of quality control procedures and documentation practices Excellent communication skills for liaising with suppliers and internal teams Ability to interpret and apply quality and legal guidelines Attention to detail and precision in executing tasks Capable of working independently with clear direction and support Nice to Have Skills: Experience working in a regulated manufacturing environment Knowledge of quality management systems (QMS) Prior experience with shift work or 12-hour rotating shifts Preferred Education and Experience: Relevant qualification in Quality Assurance, Life Sciences, or related field Previous experience in a quality control role within manufacturing or pharma sectors Seize this chance to advance your career in quality assurance! If you thrive in a fast-paced, detail-driven environment and are committed to maintaining the highest standards, we encourage you to apply now and become part of our dedicated team. #J-18808-Ljbffr
We are seeking a Lead Mechanical Design Engineer to drive the design, development and verification of complex medical devices across both capital equipment and disposable components. This is a hands?on technical leadership role where you will guide cross?functional teams, oversee full lifecycle engineering, and deliver innovative, manufacturable and compliant solutions within a regulated environment. What You’ll Do Lead the end?to?end design, development and verification of complex assemblies, sub?assemblies, components and packaging. Select materials, manufacturing processes, tooling and automation solutions to meet performance, cost and scalability needs. Translate product requirements into detailed engineering specifications and conduct feasibility studies and proof?of?concept testing. Drive design and process optimisation to improve quality, performance and manufacturability. Lead risk?management activities including PHA, FTA and dFMEA/uFMEA. Perform root?cause analysis and implement corrective actions following failure investigations. Collaborate with manufacturing teams to troubleshoot issues and refine process parameters. Manage projects or sub?projects, guide cross?functional teams and apply structured project?management methodologies. Support supplier and subcontractor activities and lead technical reviews with internal and external stakeholders. Provide team leadership including recruitment, performance oversight and daily activity coordination. Stay current with emerging engineering tools, technologies and methods to elevate team capability. What You Bring 5+ years’ experience in medical?device mechanical design, ideally spanning capital equipment and disposable components. Full product?lifecycle experience: design, development, verification and optimisation. Strong background in material selection, manufacturing processes, GD&T, DFM/DFA, DOE and root?cause analysis. Proven experience running risk?management activities (PHA, FTA, dFMEA/uFMEA). Demonstrated project and team leadership, with clear ownership of deliverables and cross?functional coordination. Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering or equivalent. Deep understanding of design for manufacturability/assembly and modern engineering practices. Strong communication skills and ability to influence decisions through technical insight. Familiarity with medical?device regulatory frameworks (ISO 13485, MDR, FDA 21 CFR 820). #J-18808-Ljbffr
Planet Pharma Group is looking for a Lead Mechanical Design Engineer in Limerick, Ireland. The candidate will drive the design and development of complex medical devices, managing full lifecycle engineering. Key responsibilities include overseeing project teams, optimizing design processes, and ensuring compliance with medical device regulations. A Bachelor’s or Master’s degree in Mechanical or Biomedical Engineering and 5+ years in medical device design are required. This role offers an opportunity to innovate and lead within a regulated environment. #J-18808-Ljbffr
