<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="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="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="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="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="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>

<div data-oe-version="1.2" data-last-history-steps="2581084492194945">We’re seeking a detail-oriented Production Documentation Officer to manage GMP-related documents and support packaging launches, scheduling, and compliance.</div><div>A degree in Chemistry or Pharmaceutical Science is required; prior experience in a GMP/production setting and SAP knowledge are advantageous.</div><div>Enjoy professional development, a performance bonus, health insurance, and a collaborative, employee-focused workplace.</div>

<div data-oe-version="1.2" data-last-history-steps="4438578250538294">The Planning Manager leads production planning and demand forecasting to optimize site efficiency and meet customer requirements.</div><div>Collaborates cross-functionally with Operations, Procurement, and Customer Service to support new product launches and ensure on-time delivery.</div><div>Ideal for a supply chain professional with pharmaceutical or FMCG experience, strong analytical skills, and proficiency in SAP or similar ERP systems.</div>

<div data-oe-version="1.2" data-last-history-steps="117426806498099">We’re looking for a skilled Maintenance Technician to perform preventive and corrective maintenance, calibrations, and equipment upkeep across our facilities.</div><div>A technical qualification is required; an Electrical Licence (Category B) and prior experience in pharma or shift-based work are considered strong assets.</div><div>Enjoy a stable role with growth opportunities, competitive salary, health insurance, and a supportive, team-driven work environment.</div>

<div data-oe-version="1.2" data-last-history-steps="4035791370095648">Seeking a Responsible Person (RP) Officer to manage quality systems including change control, audits, LIMS, and vendor qualification in compliance with GDP regulations.</div><div>Key responsibilities include audit readiness, document control, risk assessments (e.g., nitrosamines), and RP duties for controlled drugs.</div><div>Ideal candidates hold a life sciences/pharmacy degree, have 2–3 years’ pharma QA/QS experience, and strong problem-solving and communication skills.</div>