We are currently working with companies within the Pharmaceutical Manufacturing Industry who are on the lookout for a Qualified Person to join their team within the QA Department.
- Playing a crucial role in the PxLT group as a key Quality representative, managing Projects, Programs, and Products
- Participating in all aspects of batch certification, product release, and treatment of deviations
- Being the primary client interface for issues pertaining to quality for certain molecules
- Performing validation documentation review and approval while analysing and evaluating change control records, non-conformances, and CAPAs
- Leading and participate in internal and external audits and regulatory inspections
- Assisting in Quality, Production, Warehouse, and Supply Chain in ensuring that quality rules, standards, and procedures are being followed
- Participate in local and global Quality initiatives as a site subject matter expert whilst participating actively or leading projects and improvement efforts including product launches
- Performing other QA activities within the Operations, Systems or Validation respective sections according to business exigencies and the candidate's expertise
Skill-sets and Requirements
- Communication skills in English and Maltese both verbally and written
- Multitasking and organisation skills
- Must be able to manage multiple tasks
- Analysing and troubleshooting problems, identifying solutions, recommending and implementing methods, procedures and/or techniques for resolution
Education & Experience
- Tertiary degree level of education in a related field
- Proven previous experience working as a qualified person, complemented with pharma quality system knowledge
- Preference will be given to applicants being pharmacists of responsible person
Job Reference: CU811
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