Qualified Person

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Hal Fartime type:
Full time posted on:
Posted 2 Days Agojob requisition :
R26 55"Expect to grow", personally and professionally:
At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.
** Your Role:
** We are seeking an eligible QP to join our QA team in Malta, in accordance with MMA guidelines, responsible for the compliant certification and release of medicinal products and for supporting effective site quality oversight and continuous improvement.
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.
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* Your Profile:

*** A 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.
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* Your Benefits:

*** An attractive and competitive remuneration package, aligned with experience and responsibilities.
* Opportunities for professional and career growth within a global pharmaceutical organisation.
* A collaborative, quality-driven environment that values expertise, ownership, and continuous improvement.

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof.

This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.### Our purpose drives us to be the strongest team Application Submission & Screening:
Share your qualifications and enthusiasm through our application process. We review each submission to identify candidates whose skills best match the role.
Initial Interview:
We’ll explore your background, aspirations, and how you could contribute to our mission and culture.
On-Site Interview:
If possible, we invite you to meet us in person, connect with future colleagues, and get a feel for our workspace.
Offer Stage:
Congrats! If selected, you'll receive a detailed offer including compensation, benefits, and the exciting opportunities ahead.
Onboarding:
After you accept, we’ll guide you through a smooth, tailored onboarding experience to help you settle into your new role.
Feedback & Improvement:
Your feedback helps us continuously improve and enhance the candidate experience for others.
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