Aptar Italia S.P.A.

Aptar Italia S.P.A. is seeking a Quality Manager based in Cwmbran, United Kingdom. This role involves overseeing day-to-day Quality Assurance operations and ensuring compliance with GMP and regulatory standards. The ideal candidate will have extensive experience in Quality Assurance within a GMP-regulated environment and will be responsible for conducting audits, coaching staff, and maintaining quality systems. Aptar offers a competitive salary and innovative benefits plan, promoting diversity and personal development.

Nanopharm, an Aptar Pharma Company, is a world leading specialist contract research and development organization offering product development services for orally inhaled and nasal drug products (OINDPs). Nanopharm operates a fee-for-service model, helping its clients navigate the scientific, technical and regulatory challenges in developing nasal and respiratory drug products from discovery through to clinical investigations ('IND'). Its service offerings provide the most efficient path to success for its clients by providing an integrated product development service covering: Advanced materials characterization Analytical method development Formulation development and testing Inhaled biopharmaceutics These early phase services aid successful product development by understanding how material properties and processing conditions influence product functionality and therefore reduce risks and expedite drug development timelines. Nanopharm's proprietary technology and analytical platforms for advanced materials characterization, formulation & device development and in-silico modelling of in vivo behaviour, have provided Nanopharm a technical competitive edge, helping it become an international market leader. For more information visit: You should work here because we: Attract and develop high performing people. Promote a diverse and inclusive work environment. Allow for failure by allowing people to make mistakes through an open and trusting environment. Invest in the development of employees through local, regional and global career opportunities. Contribute to the communities where we reside. What's new with Aptar Nanopharm is a prominent player in the Inhalation industry, with our laboratory service provision in Wales, United Kingdom. We specialise in the development and testing of inhalable and nasal pharmaceutical products, collaborating closely with pharmaceutical companies to ensure product safety, efficacy, and regulatory compliance. Nanopharm operates as a contract research and laboratory services organisation within the Aptar Pharma group, delivering GMP and non GMP services to a global pharmaceutical client base. The site operates within a regulated environment where quality, compliance, and scientific integrity are integral to all activities. We have an exciting position open at Nanopharm, which is an Aptar Pharma Company: Quality Manager reporting into Head of Quality. These positions will be based in Cwmbran and will involve conducting pharmaceutical product analysis for our customers to a high degree of precision and efficiency. This is how your journey begins: Role Overview The Quality Manager is responsible for the day-to-day management and delivery of Quality Assurance operations, ensuring that GMP and non GMP activities are performed in compliance with regulatory requirements, company procedures, and client commitments. The role provides hands on QA leadership across routine quality system activities, laboratory oversight, internal and supplier audit programmes, and inspection readiness. The post holder applies pragmatic, risk based quality judgement appropriate to a contract laboratory operating mixed regulated and non regulated activities. The Quality Manager acts as a senior quality practitioner and people manager, supporting operational teams, coaching staff in GMP and non GMP expectations, and deputising for the Head of Quality as required. Job descriptions cover approximately 85% of a role and are not an exhaustive list of responsibilities and duties. You are expected to carry out other activities that are within reasonable scope of the role. Day to Day QA Operations & Compliance Provide routine, hands on QA oversight of GMP and non GMP laboratory activities. Maintain effective day to day operation of the Pharmaceutical Quality System (PQS), including deviations, CAPAs, change controls, Laboratory Investigations, quality records and management of quality events. Ensure quality events are assessed, investigated and closed in a compliant, timely and risk based manner. Perform or support batch, data and documentation review activities where required. Ensure QA oversight remains proportionate, risk based and appropriate to the nature of the work undertaken. Lead, perform and report internal audits in accordance with the site audit programme. Plan and conduct supplier audits and supplier quality assessments, supporting supplier qualification and ongoing performance monitoring. Review and assess supplier quality documentation to support approval and continued use. Act as a key Quality representative during client audits and regulatory inspections. Coordinate responses to audit observations, including oversight of CAPAs and effectiveness checks. Quality Systems, Data Integrity & Compliance Support maintenance and continuous improvement of the PQS, ensuring procedures are current, effective and consistently applied. Apply data integrity principles and CSV expectations across GxP systems and supporting tools. Ensure compliance with EU GMP (including Annex 11), FDA 21 CFR Parts 210/211, FDA 21 CFR Part 11, and ICH Q8, Q9 and Q10. Leadership & People Management Line manage 2 QA direct reports and provide functional oversight and mentoring to up to 4 indirect reports. Support training, coaching and competency development across QA and operational teams. Provide clear, consistent and authoritative QA guidance in an approachable and collaborative manner. Identify and drive improvements to QA processes, systems and ways of working. Support or lead implementation and optimisation of electronic Quality Management Systems (eQMS). Actively promote a strong quality culture and continuous improvement mindset across the site. Basics Always promote Nanopharm & Aptar's best interests by the positive and effective way you perform your duties modelling our Core Values and Rules of Leadership. Always comply and proactively engage with Environment, Health, Safety and Sustainability policies, procedures and instructions to ensure the safety of you and your colleagues. Always comply and proactively engage with Quality policies, procedures and instructions to ensure we deliver quality work, data and reports. Read and understand all assigned Standard Operating Procedures (SOPs) via the Quality Management System (QMS) in the timeframe specified. Maintain an up to date training record and submit to your line manager at least annually for review, making updates and amendments as necessary. Complete timesheets, expenses claims, objectives and appraisals in a timely manner as specified by Stakeholders and in line with the relevant company policies. Ensure confidential information pertaining to the company is not divulged to 3rd parties without the appropriate permission. Ensure use of IT equipment (e.g. phones, laptops, etc.) is in line with the appropriate Aptar policies. EDUCATION, Experience & RELEVANT Skills Education & Qualification Preferably a first degree in a science, pharmacy or relevant discipline of grade 2.1 or above. Experience Significant experience working in Quality Assurance within a GMP regulated environment. Experience operating in a contract laboratory or service based organisation conducting GMP and non GMP activities. Demonstrable experience of conducting internal audits and supplier audits. Experience supporting and hosting client and regulatory inspections. Experience implementing or significantly enhancing electronic Quality Management Systems (eQMS). Skills Strong working knowledge of EU GMP, FDA CFRs, Annex 11 and ICH Q8, Q9 and Q10. Sound understanding of data integrity and CSV principles. Proven ability to apply pragmatic, risk based QA decision making. Approachable, credible and collaborative leadership style. Confident communicator with internal stakeholders, clients and regulators. Practical, solution focused and calm under inspection conditions. Strong personal commitment to quality, compliance and continuous improvement. Demonstrated proactive and organised approach, able to exert influence over those whom they do not have direct authority and proven ability to prioritise and manage multiple tasks. Excellent customer related experience and customer facing skills, with the drive to ensure that this ethos is instilled within your team. Ability to communicate and work with personnel of all levels, internally and externally. Proven flexibility in adjusting to a rapidly evolving workload and remaining calm under pressure. Displays adherence to and promotion of the company values at all times. What we offer: An exciting, diverse and value based working environment. Award winning corporate university offering personal development and training opportunities. Competitive base salary and performance based bonus plan. Innovative benefits plan, which includes: medical, life, disability and wellness. Be You. Be Aptar Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief. . click apply for full job details

Aptar Italia S.P.A. is seeking a Quality Technician based in Leeds, UK. This fully onsite role involves working 42 hours per week, ensuring all products meet quality standards while fostering a strong quality culture. The ideal candidate will possess a third-level qualification in Quality, Science, Engineering, or Plastics, along with strong analytical skills and the ability to thrive in a fast-paced manufacturing environment. Key responsibilities include compliance checks, product testing, and managing quality audits.

About the Role Aptar is seeking a Quality Technician based in Leeds, UK. This is a fully onsite role working 42 hours per week across a rotating shift pattern (12 hour day and night shifts, Monday to Sunday). As a Quality Technician, you will play a key role in ensuring that all products dispatched to customers meet internal and external quality requirements while supporting a strong quality culture across the site. Responsibilities Ensure compliance with all relevant Health, Safety, Welfare and Environmental regulations and Company requirements Promote a strong quality culture, including training colleagues on product safety and hygiene standards Carry out product testing using supplied measuring equipment to agreed specifications Analyse test data, interpret results, and produce accurate reports Manage calibration of equipment in line with company management systems Lead quality investigations relating to customer complaints, supplier issues, audits, and quarantined stock Raise and manage supplier complaints regarding non conforming raw materials Maintain accurate records in accordance with company management systems Generate and communicate quality reports (complaints, supplier performance, audit results) Conduct microbiological sampling on required products Support internal and third party audits Review quality documents and supplier records (CoA, CoC) to ensure compliance Participate in continuous improvement initiatives and complete corrective actions Provide support to production colleagues and adapt flexibly to business needs Who We are Looking For We're seeking a detail oriented, proactive individual with strong analytical skills and the ability to work independently. The ideal candidate thrives in a fast paced manufacturing environment, demonstrates sound decision making based on data, and communicates effectively across teams. Education Third level qualification or equivalent in Quality, Science, Engineering, or Plastics Required Skills Strong communication and organisational skills Ability to work effectively as part of a team Self motivated, detail oriented, and diligent Problem solving skills and ability to work independently Proficient in internal systems such as SAP and Microsoft Office Preferred Skills Knowledge of industry standards (BRC, ISO 9001, HACCP, GMP) Experience using precision metrology tools (CMM, calipers, micrometers, gauges, force testers) Familiarity with statistical methods for quality control Experience with internal audit processes Ability to draft reports and collate data Experience in a fast paced manufacturing environment Benefits An exciting, diverse and value based working environment Award winning corporate university offering personal development and training opportunities Competitive base salary and performance based bonus plan 280 hours of vacation at the start, life insurance cover at the level of 4 times basic salary Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief.

Aptar Italia S.P.A. in Leeds is looking for a Quality Technician to ensure compliance with quality standards. This fully onsite role involves product testing, quality reporting, and supporting a strong quality culture. The ideal candidate should have a third-level qualification in a relevant field and strong communication skills. The position offers a competitive salary, 280 vacation hours, and other benefits.

About the Role Aptar is seeking a Quality Technician based in Leeds, UK. This is a fully onsite role working 42 hours per week across a rotating shift pattern (12 hour day and night shifts, Monday to Sunday). As a Quality Technician, you will play a key role in ensuring that all products dispatched to customers meet internal and external quality requirements while supporting a strong quality culture across the site. Responsibilities Ensure compliance with all relevant Health, Safety, Welfare and Environmental regulations and Company requirements Promote a strong quality culture, including training colleagues on product safety and hygiene standards Carry out product testing using supplied measuring equipment to agreed specifications Analyse test data, interpret results, and produce accurate reports Manage calibration of equipment in line with company management systems Lead quality investigations relating to customer complaints, supplier issues, audits, and quarantined stock Raise and manage supplier complaints regarding non conforming raw materials Maintain accurate records in accordance with company management systems Generate and communicate quality reports (complaints, supplier performance, audit results) Conduct microbiological sampling on required products Support internal and third party audits Review quality documents and supplier records (CoA, CoC) to ensure compliance Participate in continuous improvement initiatives and complete corrective actions Provide support to production colleagues and adapt flexibly to business needs Who We are Looking For We're seeking a detail oriented, proactive individual with strong analytical skills and the ability to work independently. The ideal candidate thrives in a fast paced manufacturing environment, demonstrates sound decision making based on data, and communicates effectively across teams. Education Third level qualification or equivalent in Quality, Science, Engineering, or Plastics Required Skills Strong communication and organisational skills Ability to work effectively as part of a team Self motivated, detail oriented, and diligent Problem solving skills and ability to work independently Proficient in internal systems such as SAP and Microsoft Office Preferred Skills Knowledge of industry standards (BRC, ISO 9001, HACCP, GMP) Experience using precision metrology tools (CMM, calipers, micrometers, gauges, force testers) Familiarity with statistical methods for quality control Experience with internal audit processes Ability to draft reports and collate data Experience in a fast paced manufacturing environment Benefits An exciting, diverse and value based working environment Award winning corporate university offering personal development and training opportunities Competitive base salary and performance based bonus plan 280 hours of vacation at the start, life insurance cover at the level of 4 times basic salary Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief.