Torrent Pharma (Malta) Limited

Torrent Pharma (Malta) Limited: Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country. The Company was a pioneer in initiating the concept of niche marketing in India and today is ranked amongst the leaders in the therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastrointestinal (GI) and women's healthcare (WHC). The Company also has a significant presence in diabetology, pain management, gynaecology, oncology and anti-infective segments.

We are currently looking for a Senior Quality Assurance Officer (Quality Operations) to join our team.&nbsp;
In this role, you will play a pivotal role in upholding our commitment to quality and compliance. You will collaborate with a cross-functional team to ensure that Batch Documentation Package required for Batch Certification activities adhere to GMP standards, company procedures, and regulatory guidelines.&nbsp;
Key Responsibilities: 
<ul>
<li>Support the maintenance and continuous improvement of the Quality Management System (QMS) in compliance with GMP requirements and regulatory standards.&nbsp;</li>
<li>Assist the Qualified Person (QP) with batch certification activities, including the review of batch documentation to ensure compliance with approved product dossiers and marketing authorisations.&nbsp;</li>
<li>Collaborate with Contract Manufacturing Organisations (CMOs) and internal stakeholders to resolve documentation issues and support the timely closure of deviations, CAPAs, and change controls.&nbsp;</li>
<li>Manage quality-related activities including Product Quality Reviews (PQRs), market complaints, audit documentation, change evaluations, and QP declarations in accordance with company procedures.&nbsp;</li>
<li>Participate in self-inspections and external audits, providing quality assurance support to maintain compliance and drive continuous improvement.</li>
</ul>

Job Requirements: 
<ul>
<li>Degree in a scientific field (Chemistry, Pharmacy, or related discipline)</li>
<li>Minimum of 4 years of experience in pharmaceutical quality assurance or a related field</li>
<li>Demonstrated expertise in GMP principles and regulatory requirements</li>
<li>Strong QA skills and meticulous attention to detail</li>
<li>Excellent communication and interpersonal skills, with fluency in English (both written and verbal)</li>
<li>Proactive, results-oriented, and capable of working independently and as part of a team</li>
</ul>

What we offer: 
<ul>
<li>Competitive remuneration package</li>
<li>Comprehensive health insurance</li>
<li>Continuous professional growth opportunities in a state-of-the-art Testing and Batch Certification Facility.</li>
</ul>

We are currently looking for a Senior Quality Assurance Officer (Quality Operations) to join our team.&nbsp;
In this role,  you will play a pivotal role in upholding our commitment to quality and...

Senior Quality Assurance Officer (Quality Operations)

We are currently looking for an Analytical Quality Assurance Officer to join our team.&nbsp;
As an AQA Officer, you will play a pivotal role in upholding our commitment to quality and compliance. You will collaborate with a cross-functional team to ensure that all analytical activities adhere to GMP standards, company procedures, and regulatory guidelines.&nbsp;
Key Responsibilities: 
<ul>
<li>Manage day-to-day Analytical Quality Assurance activities, ensuring strict adherence to GMP directives and guidelines</li>
<li>Prepare, review, and approve analytical worksheets, LIMS Master data, protocols, SOPs, and reports</li>
<li>Coordinate analytical method transfers, including comprehensive documentation review</li>
<li>Investigate out-of-specification results and laboratory deviations, driving root cause analysis and corrective actions</li>
<li>Review and approve instrument calibration, qualification, and analytical data, ensuring accuracy and reliability</li>
<li>Collaborate with internal and external stakeholders to maintain a robust quality system</li>
</ul>

Job Requirements: 
<ul>
<li>Degree or diploma in a scientific field (Chemistry, Pharmacy, or related discipline)</li>
<li>Minimum of 2 years of experience in pharmaceutical quality assurance or a related field</li>
<li>Demonstrated expertise in GMP principles and regulatory requirements</li>
<li>Strong analytical skills and meticulous attention to detail</li>
<li>Excellent communication and interpersonal skills, with fluency in English (both written and verbal)</li>
<li>Proactive, results-oriented, and capable of working independently and as part of a team</li>
</ul>

What we offer: 
<ul>
<li>Competitive remuneration package</li>
<li>Comprehensive health insurance</li>
<li>Continuous professional growth opportunities in a state-of-the-art laboratory equipped with the latest technologies</li>
</ul>

We are currently looking for an Analytical Quality Assurance Officer to join our team.&nbsp;
As an AQA Officer, you will play a pivotal role in upholding our commitment to quality and compliance. You...

Analytical Quality Assurance Officer

At Torrent Pharma Malta, our people are central to our continued growth and success. We are committed to creating a working environment in which employees are respected, listened to, supported in their wellbeing and encouraged to learn, develop and contribute.
As part of an international pharmaceutical group and a growing organisation in Malta, we offer the opportunity to work alongside dedicated professionals who share a commitment to quality, integrity, teamwork and continuous improvement.
We are always interested in connecting with talented and motivated individuals who would like to develop their careers within the pharmaceutical industry.
While a suitable vacancy may not be available at present, joining our Talent Pool enables us to consider your profile when relevant opportunities arise.
Why consider a career with us?
<ul>
<li>Contribute to meaningful work within the pharmaceutical industry</li>
<li>Develop your knowledge, skills and professional experience</li>
<li>Work in an environment built on respect, inclusion and teamwork</li>
<li>Be part of a culture that values employee contribution and continuous improvement</li>
<li>Grow alongside an organisation with ambition and a clear future</li>
<li>Benefit from the experience and international reach of the wider Torrent Group</li>
</ul>
Why join our Talent Pool?
<ul>
<li>Be considered for relevant future career opportunities</li>
<li>Introduce yourself and share your career aspirations</li>
<li>Explore opportunities aligned with your qualifications, skills and experience</li>
<li>Stay connected with Torrent Pharma Malta as our organisation continues to grow</li>
<li>If you are interested in building your future with us, we invite you to join our Talent Pool and submit your CV today.</li>
</ul>
We look forward to learning more about you.
Joining our Talent Pool does not guarantee employment or consideration for a specific vacancy. Personal data will be processed in accordance with our applicable Privacy Notice.
&nbsp;

At Torrent Pharma Malta, our people are central to our continued growth and success. We are committed to creating a working environment in which employees are respected, listened to, supported in...

Join Our Talent Pool!

We are looking for a detail-oriented and experienced Senior Quality Assurance Officer (Quality Management Systems &amp; EOHS) to support the maintenance and continuous improvement of our Quality Management System (QMS) and Environment, Occupational Health &amp; Safety (EOHS) Management System, ensuring continued compliance with applicable regulatory and company requirements.
The role reports directly to the Quality Management Systems Manager.
Key Responsibilities:
<ul>
<li>Prepare, update and maintain SOPs/SOFs in accordance with company policies, EU cGMP requirements and applicable EOHS requirements.</li>
<li>Support the preparation for regulatory and client audits and participate in the company's self-inspection programme.</li>
<li>Maintain QA documentation, quality logs, document registers and associated records to ensure continued compliance.</li>
<li>Assist in the investigation, follow-up and closure of deviations.</li>
<li>Collaborate cross-functionally with internal departments to ensure that quality, regulatory and EOHS requirements are effectively integrated into company processes.</li>
<li>Assist in the implementation and maintenance of the company's training programme and ensure that required employee training is appropriately managed and documented.</li>
<li>Manage the Supplier Qualification Programme.</li>
<li>Review Corrective and Preventive Actions (CAPAs), monitor their implementation and effectiveness, and support the overall CAPA Programme as part of continuous improvement.</li>
<li>Support the external audit programme.</li>
<li>Assist in the registration, follow-up, risk assessment and closure of change controls.</li>
<li>Assist in the review of asset calibration and/or qualification documentation.</li>
<li>Maintain and support the company's EOHS Management System, ensuring that relevant procedures, records and programmes remain current and effectively implemented.</li>
<li>Coordinate and follow up on EOHS risk assessments, inspections, incidents, near misses and associated corrective/preventive actions.</li>
<li>Support the implementation and monitoring of occupational health and safety, environmental, emergency preparedness and workplace safety programmes.</li>
<li>Maintain applicable EOHS documentation, registers, records and training requirements and support compliance with applicable legislation and company standards.</li>
<li>Participate in EOHS audits, inspections and continuous improvement initiatives, following up on identified actions through to closure.</li>
</ul>

Requirements:
<ul>
<li>Bachelor's degree or higher in Pharmacy, Life Sciences, or a related discipline.</li>
<li>Minimum of 4 years' experience in Quality Management within the pharmaceutical industry.</li>
<li>Sound knowledge of EU cGMP and applicable local regulatory requirements.</li>
<li>Knowledge or experience in Environment, Occupational Health &amp; Safety (EOHS) systems would be considered an asset.</li>
<li>Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.</li>
<li>Strong organisational and problem-solving skills, with a high level of attention to detail.</li>
<li>Ability to manage multiple priorities and follow actions through to completion.</li>
<li>Must be in a possession of a valid work permit&nbsp;</li>
</ul>

What We Offer:
<ul>
<li>Competitive remuneration package.</li>
<li>Comprehensive health insurance.</li>
<li>Continuous professional growth and development opportunities.</li>
<li>The opportunity to work in a state-of-the-art Testing and Batch Certification Facility within a dynamic pharmaceutical quality environment.</li>
</ul>

We are looking for a detail-oriented and experienced Senior Quality Assurance Officer (Quality Management Systems &amp; EOHS) to support the maintenance and continuous improvement of our Quality...

Senior Quality Assurance Officer (Quality Management Systems & EOHS)

We are looking for a highly experienced Deputy Regulatory Affairs Manager - EU Lifecycle Management to support our growing EU Regulatory Affairs function.&nbsp;
This is a senior, hands-on role focused on EU post-authorisation lifecycle management, including safety-related and CMC-related regulatory activities.
Key Responsibilities:
<ul>
<li>Manage and support EU lifecycle submissions, including Type IA, IAIN, IB and Type II variations.</li>
<li>Provide regulatory strategy for variation classification, grouping, work-sharing, implementation dates and submission planning.</li>
<li>Support safety-related lifecycle updates, including Product Information updates, RMP-related changes, PSUR outcomes, referrals and reference product updates.</li>
<li>Support CMC lifecycle changes, including manufacturing site changes, analytical methods, specifications, stability, suppliers, packaging, batch release and testing sites.</li>
<li>Prepare, review and coordinate SmPC, labelling and package leaflet updates.</li>
<li>Support responses to authority questions, validation issues and clock-stops.</li>
<li>Liaise with corporate RA teams, internal departments, external partners, consultants and regulatory authorities.</li>
<li>Mentor RA team members and support development of RA procedures, trackers and working practices.</li>
</ul>

Requirements:
<ul>
<li>Degree in Pharmacy, Life Sciences, Pharmaceutical Sciences, Chemistry or related discipline.</li>
<li>Minimum 10 years’ Regulatory Affairs experience within the pharmaceutical industry.</li>
<li>Strong hands-on experience in EU post-authorisation lifecycle management.</li>
<li>Experience with both safety-related and CMC-related variations.</li>
<li>Good knowledge of DCP, MRP and national procedures.</li>
<li>Strong understanding of EU variation requirements, CMDh/HMA guidance, eAF requirements and regulatory submission processes.</li>
<li>Experience reviewing submissions and identifying regulatory gaps before filing.</li>
<li>Excellent organisational, communication and problem-solving skills.</li>
<li>Fluent written and spoken English.</li>
</ul>

Preferred Experience:
<ul>
<li>Experience with generic medicinal products.</li>
<li>Experience with multi-country EU regulatory portfolios.</li>
<li>Experience with eCTD lifecycle submissions and electronic submission systems.</li>
</ul>

What We Offer: 
<ul>
<li>Competitive remuneration package.</li>
<li>Comprehensive health insurance.</li>
<li>Professional development and training opportunities.</li>
<li>Exposure to a broad European pharmaceutical portfolio.</li>
<li>Opportunity to contribute to the development of a growing EU Regulatory Affairs function in Malta.</li>
</ul>

We are looking for a highly experienced Deputy Regulatory Affairs Manager - EU Lifecycle Management to support our growing EU Regulatory Affairs function.&nbsp;
This is a senior, hands-on role...

Deputy Regulatory Affairs Manager - EU Lifecycle Management

We are seeking an experienced Regulatory Affairs Specialist to support our growing EU Regulatory Affairs function.
This role is focused on EU post-authorisation lifecycle management, including safety-related and CMC-related regulatory activities.

Key Responsibilities:
<ul>
<li>Prepare, review and support EU lifecycle submissions, including Type IA, IAIN, IB and Type II variations.</li>
<li>Support variation classification, grouping, worksharing, implementation dates and submission planning.</li>
<li>Support safety-related lifecycle updates, including Product Information updates, RMP-related changes, PSUR outcomes, referrals and reference product updates.</li>
<li>Support CMC lifecycle changes, including manufacturing site changes, analytical methods, specifications, stability, suppliers, packaging, batch release and testing sites.</li>
<li>Prepare, review and coordinate SmPC, labelling and package leaflet updates.</li>
<li>Support renewals, regulatory commitments and lifecycle tracking activities.</li>
<li>Prepare and support responses to authority questions, validation issues and clock-stops.</li>
<li>Liaise with corporate RA teams, internal departments, external partners, consultants and regulatory authorities.</li>
<li>Maintain RA trackers, submission plans and regulatory documentation.</li>
<li>Contribute to the development of RA procedures, templates and working practices.</li>
</ul>

Requirements:
<ul>
<li>Degree in Pharmacy, Life Sciences, Pharmaceutical Sciences, Chemistry or related discipline.</li>
<li>Minimum 5 years’ Regulatory Affairs experience within the pharmaceutical industry.</li>
<li>Hands-on experience in EU post-authorisation lifecycle management.</li>
<li>Experience with safety-related and/or CMC-related variations.</li>
<li>Good knowledge of DCP, MRP and national procedures.</li>
<li>Understanding of EU variation requirements, CMDh/HMA guidance, eAF requirements and regulatory submission processes.</li>
<li>Ability to review regulatory documentation and identify gaps before submission.</li>
<li>Excellent organisational, communication and problem-solving skills.</li>
<li>Fluent written and spoken English.</li>
<li>Eligibility to work in Malta / EU.</li>
</ul>

Preferred Experience:
<ul>
<li>Experience with generic medicinal products.</li>
<li>Experience with multi-country EU regulatory portfolios.</li>
<li>Experience with eCTD lifecycle submissions and electronic submission systems.</li>
</ul>

What We Offer:
<ul>
<li>Competitive remuneration package.</li>
<li>Comprehensive health insurance.</li>
<li>Professional development and training opportunities.</li>
<li>Exposure to a broad European pharmaceutical portfolio.</li>
<li>Opportunity to contribute to the development of a growing EU Regulatory Affairs function in Malta.</li>
</ul>

We are seeking an experienced Regulatory Affairs Specialist to support our growing EU Regulatory Affairs function.
This role is focused on EU post-authorisation lifecycle management, including...

Regulatory Affairs Specialist – EU Lifecycle Management

We are looking for a motivated and experienced Senior QC Analyst to join our growing team. In this role, you will work in a GMP-compliant chemistry laboratory, where your expertise will directly contribute to delivering high-quality finished products.
Key Responsibilities:
<ul>
<li>Prepare, standardise and label stock solutions and laboratory reagents as required.</li>
<li>Perform finished product and purified water testing using approved methods and specifications.</li>
<li>Ensure proper handling, qualification, and calibration of laboratory equipment, including supporting external contractors and maintaining accurate records.</li>
<li>Maintain and review QC documentation, SOPs, logs, and registers to ensure ongoing compliance.</li>
<li>Support QC investigations, including deviations, OOX results, and change controls, and where required provide guidance to junior analysts.</li>
<li>Carry out other Quality Control-related duties as required.</li>
</ul>

Job Requirements:
<ul>
<li>Degree or diploma in a scientific field.</li>
<li>Minimum of 3 years of experience in a pharmaceutical QC laboratory, with strong expertise in chromatographic techniques.</li>
<li>Excellent attention to detail, well-organised, and able to prioritise tasks effectively.</li>
<li>Excellent communication skills.</li>
<li>Valid work permit.</li>
</ul>

What we offer: 
<ul>
<li>Competitive remuneration package with regular reviews and salary progression.</li>
<li>Continuous professional development opportunities in a state-of-the-art, brand-new laboratory equipped with the latest technologies.</li>
<li>Comprehensive health insurance.</li>
</ul>

We are looking for a motivated and experienced Senior QC Analyst to join our growing team. In this role, you will work in a GMP-compliant chemistry laboratory, where your expertise will directly...