Validation Site Program Manager
- Field
- Management
- Salary
- Salary undisclosed
- Location
- Oevel-Westerlo
- Employment
- Permanent
- Headhunter
- QTC Recruitment
More € 100K+ jobs
The organisation
For an organisation that is a global and leading manufacturer and marketer of high-quality care products, we are currently looking for a Validation Site Program Manager. Their products are currently sold in over 150 countries under several, well-known brands. As the global leader with a focus on prestige cosmetics, they touch over half a billion consumers a year.
The position
The Validation department supports the production site in developing, implementing and pragmatically improving validation processes in line with cGMP requirements. The main responsibility consists of compiling, executing and coordinating various validation activities. This means that, in collaboration with QA Compliance, you quickly and effectively implement the validation approach for large and small investment projects, as well as for process changes, e.g. cGMP guidelines, risk analyses and internal procedures. You also increase the level of compliance in production without sacrificing a pragmatic approach, especially regarding procedures and policies regarding IQ, OQ, PQ, PPQ validation, change control and the management of open deviations (deviations). You monitor the cGMP and qualification aspects in projects, by ensuring a thorough Impact Assessment of changes and by ensuring that the critical aspects are anchored in the associated qualification and validation plans and protocols. In addition, you support your colleagues and manager during visits, audits or contacts with Regulatory agencies.
Candidate profile
If you are a decisive professional with a master's degree and expertise in the field of validation according to the latest industry practices/cGMP, then this might be just the role for you. Furthermore, you:
- Have experience with FDA Regulated industries (Medical Devices or pharmaceuticals);
- Have extensive experience in writing and executing protocols, including complex systems such as Process Validation, Cleaning Validation, materials and formula systems;
- Can manage complex projects and others describe you as a strong leader, manager, or coach with an eye for people and the organisation;
- Have strong problem-solving skills and fluent knowledge of English and the usual MS Office applications.
The offer
Due to the organisation's growth, they are now going through an interesting phase. For the first time, they will have a biological manufacturing site in Belgium. You will come across an organisation that is passionate about its products. Empowered to apply their talents and diverse perspectives in an inclusive culture, their shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of their colleagues.
The organisation is also able to offer you:
- Competitive package with fringe benefits;
- Excellent personal and growth package;
- Being part of a stable and growing organisation;
- A dynamic environment offers you room to develop different skills and provide your input in the development of processes.
Interested?
You can apply to this position by using the link below.
About this headhunter - QTC Recruitment
At QTC Recruitment, we stand as the foremost niche recruitment agency in the Benelux for the Life Science industry. Renowned for our unwavering commitment to quality, unparalleled market knowledge, and expansive network, we specialize in forging the perfect match between exceptional professionals and thriving organizations, whether they're embarking on their journey, expanding, or already established.