The Medical Devices Responsible Person (MDRP) ensures full compliance with medical device regulations and maintains the Quality Management System within the organization.

This role involves regulatory affairs support, inventory and complaint management, internal audits, and coordination with local authorities.

Ideal for a detail-oriented professional registered with the Malta Medicines Authority, with experience in regulatory affairs and quality systems.

We’re hiring a Warehouse & Material Handler to oversee material assignment, storage, stock control, and hygiene compliance in a GMP-regulated environment.

Applicants must be organised, shift-ready, computer literate, and fluent in English and Maltese; experience in pharma/GMP is an asset.

Enjoy a stable role with health insurance, ongoing training, and a supportive, team-driven workplace culture.

The role involves performing routine and advanced analyses on raw materials, in-process products, finished goods, and stability samples following internal procedures. The candidate will support method development, validation, and transfers, coach junior staff, maintain lab instruments, manage documentation, and ensure good housekeeping. Shift work (day, afternoon, night) is required. Only candidates with EU passports may apply.

We are seeking a QC Documentation Officer to handle preparation, review, and issuance of Quality Control documents in line with cGMP and internal procedures.

Candidates must hold a higher qualification in Chemistry or Pharmaceutical Sciences and have at least 2 years’ QC experience in a pharmaceutical setting.

Benefit from professional development, competitive pay, health insurance, and a collaborative, people-focused work environment.

We are looking for a Production Documentation Officer to manage, write, and improve critical production documents while supporting manufacturing operations and packaging launches.

A degree in Chemistry, Pharmaceutical Science, or related fields is required; prior GMP or production experience is ideal but not mandatory.

Enjoy ongoing training, performance bonuses, health insurance, and a collaborative, growth-focused work environment.

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.

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.

Join a secure and growth-oriented workplace offering health benefits, professional development, and a supportive team culture.

Seeking a Responsible Person (RP) Officer to manage quality systems including change control, audits, LIMS, and vendor qualification in compliance with GDP regulations.

Key responsibilities include audit readiness, document control, risk assessments (e.g., nitrosamines), and RP duties for controlled drugs.

Ideal candidates hold a life sciences/pharmacy degree, have 2–3 years’ pharma QA/QS experience, and strong problem-solving and communication skills.

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.

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.

Join a supportive company offering competitive salary, professional growth, health benefits, and a strong team-oriented culture. 

The Medical Representative promotes a trusted range of infant formulas by building strong relationships with healthcare professionals and pharmacies.

This role involves scientific detailing, market analysis, and participation in medical events to support brand visibility and growth.

Ideal for a driven individual with a science background and a passion for healthcare, sales, and patient wellbeing.

The Manager of Supply Chain Logistics leads end-to-end supply operations — including forecasting, procurement, warehousing, and transportation — to support pharmaceutical launches.

The role is pivotal in driving cost efficiency, monitoring performance KPIs, and managing cross-functional teams in a fast-paced, regulated environment.

Ideal for a seasoned logistics professional with strong ERP and analytical capabilities, committed to optimizing healthcare access in underserved markets.

The Production Manager oversees pharmaceutical manufacturing operations, ensuring adherence to cGMP standards, safety protocols, and production targets.

This leadership role focuses on team development, process optimization, and cross-functional coordination to drive continuous improvement and operational excellence.

Ideal for a strategic and experienced professional with a strong background in pharmaceutical production, regulatory compliance, and lean methodologies.

The Head MDRP leads regulatory compliance and Quality Management System oversight for medical devices, ensuring adherence to Maltese and EU regulations.

Responsible for supervising and developing MDRP staff, managing audits, product complaints, recalls, and post-market surveillance activities.

Ideal for a registered MDRP with a life sciences background, strong leadership skills, and experience in regulatory affairs and quality management.