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
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