TTI International

TTI International Limited recruits and provides customized specialist manpower solutions to all industrial sectors, both in Malta and internationally.

About

Qualified Person

TTI International – Talent. Transfer. International.

BEHIND EVERY SUCCESS THERE IS TALENT.

That's why we - at TTI International - are looking for the best talents. Our vision is to unite: The best talents in the country and successful companies, which offer exciting jobs where you can realize your talents. What are you waiting for? Show us your talent and apply now!

TTI is seeking for a Qualified Person for one of our top clients. Our client is a leading entity in Pharmaceutical Services.

Main tasks and responsibilities

Oversee and actively participate in the batch release and certification process, ensuring that all required documentation is complete, accurate, and compliant prior to release
Serve as the primary quality contact for assigned clients, addressing quality-related matters, deviations, and product complaints in a timely and compliant manner
Perform review and approval of validation- and GMP-related documentation, including change controls, deviations/non-conformances, and CAPAs, ensuring appropriate risk assessment and regulatory impact evaluation
Lead or support internal and external audits, as well as regulatory inspections including preparation, execution and follow-up activities
Provide technical guidance and oversight to Quality, Production, Warehouse, and Supply Chain functions to ensure ongoing compliance with quality systems, procedures, and regulatory expectations
Contribute as a site subject matter expert to local and global Quality initiatives, supporting projects, continuous improvement activities, and product launches , as required
Perform additional QA-related activities within the Operations, Systems or Validation functions, aligned with business exigencies and the candidate's expertise

Educational and skill requirements

Tertiary-level degree in a relevant scientific discipline, meeting all criteria as defined under EC/2001/83
Demonstrable experience performing QP duties within a GMP-regulated pharmaceutical manufacturing environment
Strong problem-solving skills, including the ability to analyse quality issues, identify root causes, and propose and support effective, compliant solutions
Pharmacist qualification and/or experience as a Responsible Person (RP) will be considered an asset.
Communicating clearly and concisely, both orally and in writing across multiple levels of the organisation
Proven ability to manage multiple priorities and assignments effectively in a regulated environment

Salary information will be provided during the interview with shortlisted candidates.

JOB ID: 12988

Advertisement published10. February 2026

Application deadline24. March 2026

Language skills

No specific language requirements

Type of work

Skills

LeadershipPhone communicationEmail communication

Professions

Job Tags

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