<div data-oe-version="1.2" data-last-history-steps="3625831138851554">We’re hiring a Warehouse &amp; Material Handler to oversee material assignment, storage, stock control, and hygiene compliance in a GMP-regulated environment.</div><div>Applicants must be organised, shift-ready, computer literate, and fluent in English and Maltese; experience in pharma/GMP is an asset.</div><div>Enjoy a stable role with health insurance, ongoing training, and a supportive, team-driven workplace culture.</div>

<div data-oe-version="1.2" data-last-history-steps="732624204137271">We are seeking a QC Documentation Officer to handle preparation, review, and issuance of Quality Control documents in line with cGMP and internal procedures.</div><div>Candidates must hold a higher qualification in Chemistry or Pharmaceutical Sciences and have at least 2 years’ QC experience in a pharmaceutical setting.</div><div>Benefit from professional development, competitive pay, health insurance, and a collaborative, people-focused work environment.</div>

<div data-oe-version="1.2" data-last-history-steps="3646684624930144">The Medical Devices Responsible Person (MDRP) ensures full compliance with medical device regulations and maintains the Quality Management System within the organization.</div><div>This role involves regulatory affairs support, inventory and complaint management, internal audits, and coordination with local authorities.</div><div>Ideal for a detail-oriented professional registered with the Malta Medicines Authority, with experience in regulatory affairs and quality systems.</div>

<div data-oe-version="1.2" data-last-history-steps="1481423555874433">We are looking for a Production Documentation Officer to manage, write, and improve critical production documents while supporting manufacturing operations and packaging launches.</div><div>A degree in Chemistry, Pharmaceutical Science, or related fields is required; prior GMP or production experience is ideal but not mandatory.</div><div>Enjoy ongoing training, performance bonuses, health insurance, and a collaborative, growth-focused work environment.</div>

<div data-oe-version="1.2" data-last-history-steps="3891912965328489">We are seeking an IT Systems Administrator to maintain and support our hardware, networks, and IT infrastructure while ensuring smooth daily operations and security compliance.</div><div>A diploma in Computer Engineering and experience in hardware, networks, and cloud platforms (especially Azure) are required; knowledge of SAP or Spanish is a plus.</div><div>Join a secure and growth-oriented workplace offering health benefits, professional development, and a supportive team culture.</div>

<div data-oe-version="1.2" data-last-history-steps="1389126747463177">We are seeking an EPHS Officer to maintain and improve Health, Safety, and Environmental systems across our sites, including compliance audits, staff training, and managing permits like IPPC and ISO 14001.</div><div>Candidates should hold a degree (Master’s preferred), have 3+ years’ experience in EPHS within pharmaceutical or chemical industries, and be proficient in English and MS Office.</div><div>Join a supportive company offering competitive salary, professional growth, health benefits, and a strong team-oriented culture.&nbsp;</div>

<div data-oe-version="1.2" data-last-history-steps="1705604963481374">The Medical Representative promotes a trusted range of infant formulas by building strong relationships with healthcare professionals and pharmacies.</div><div>This role involves scientific detailing, market analysis, and participation in medical events to support brand visibility and growth.</div><div>Ideal for a driven individual with a science background and a passion for healthcare, sales, and patient wellbeing.</div>

<div data-oe-version="1.2" data-last-history-steps="3947742509180739">The Manager of Supply Chain Logistics leads end-to-end supply operations — including forecasting, procurement, warehousing, and transportation — to support pharmaceutical launches.</div><div>The role is pivotal in driving cost efficiency, monitoring performance KPIs, and managing cross-functional teams in a fast-paced, regulated environment.</div><div>Ideal for a seasoned logistics professional with strong ERP and analytical capabilities, committed to optimizing healthcare access in underserved markets.</div>

<div data-oe-version="1.2" data-last-history-steps="1308457886705679">The Production Manager oversees pharmaceutical manufacturing operations, ensuring adherence to cGMP standards, safety protocols, and production targets.</div><div>This leadership role focuses on team development, process optimization, and cross-functional coordination to drive continuous improvement and operational excellence.</div><div>Ideal for a strategic and experienced professional with a strong background in pharmaceutical production, regulatory compliance, and lean methodologies.</div>

<div data-oe-version="1.2" data-last-history-steps="3876085309497882">The Head MDRP leads regulatory compliance and Quality Management System oversight for medical devices, ensuring adherence to Maltese and EU regulations.</div><div>Responsible for supervising and developing MDRP staff, managing audits, product complaints, recalls, and post-market surveillance activities.</div><div>Ideal for a registered MDRP with a life sciences background, strong leadership skills, and experience in regulatory affairs and quality management.</div>

<div data-oe-version="1.2" data-last-history-steps="670416661162987">oin our team as a Regulatory/Quality Support Officer, ensuring GMP compliance, supporting QPs in product release, and driving quality culture initiatives.</div><div>A degree in Pharmacy, Biology, or Chemistry is required; prior GMP quality experience and strong communication skills are considered assets.</div><div>We offer career development, health insurance, medical check-ups, and a secure, team-focused work environment.</div>

<div data-oe-version="1.2" data-last-history-steps="680112818032891">The FDF Industrialisation Manager leads the coordination of R&amp;D activities focused on process validation, technical transfers, and the industrialisation of pharmaceutical dosage forms.</div><div>The role ensures regulatory compliance with EMA and FDA standards while driving cross-functional collaboration and technical excellence.</div><div>Ideal for an experienced pharmaceutical professional with strong project management skills and a background in finished dosage form production.</div>