Join a robust and innovative team where your expertise will significantly impact the
pharmaceutical manufacturing industry
. This role requires a motivated professional ready to navigate a fast-paced technical environment.
You will fit in well as a dedicated
Cleaning Validation Specialist
if you are detail-oriented, proactive, and keen to contribute to quality assurance processes.
* You participate in functional meetings essential for executing your responsibilities.
* You work primarily during day shifts onsite but may occasionally engage in early or late shifts as required.
* You ensure continuity in assignment execution despite absences due to various reasons.
* You perform periodic reviews of cleaning processes across three production departments to maintain validation states.
* You coordinate and execute annual re-qualification studies in alignment with operational practices.
* You provide support for cleaning projects, including method development and validation.
* You handle deviation management, including documentation and root cause analysis.
What are we looking for?
* You hold a
Bachelor's degree in Chemistry, Biology, Biomedical studies
, or possess equivalent experience.
* You have relevant experience in
Pharmaceutical Processes
,
Validation
, and
Project Management
.
* You demonstrate solid technical writing skills and can apply theoretical knowledge in practical settings.
* You are a strong communicator, skilled in
team collaboration
, and bring a quality-focused mindset.
* You are flexible and committed to delivering results, with a keen interest in shop floor activities.
* You possess a strong command of
English
, encompassing speaking, writing, and reading proficiency.