Job Description
We are seeking a dedicated and detail-oriented Validation Officer to join our team. In this supporting role, you will assist the Validation Lead and Validation Engineers in upholding our commitment to Good Manufacturing Practice (GMP) standards. You will assist in the process of verifying that our products are manufactured using equipment, facilities, and processes that meet both company specifications and regulatory requirements. We invite you to apply and help us maintain the highest standards of quality in our operations.
Responsibilities
* Working as part of the Validation and Quality Assurance team in both the Office and Production facilities.
* Maintenance of the validation schedule defined in the Site Validation Master Plans.
* Author validation reviews to confirm the maintenance of validation status of equipment.
* Supporting the Validation Engineers with equipment, facilities and utilities validation activities as required.
* Providing support on major validation projects as required.
* Generating and implementing Standard Operating Procedures (SOPs) and Works Instructions (WIs) as required.
* Assisting with management of the onsite Calibration programme, including performing Internal calibrations, when necessary, to ensure equipment is calibrated on time and to an acceptable level.
* Participating in Internal and External Audit activities.
Qualifications
* Hold qualifications in a scientific or engineering field or have some equivalent experience.
* IT literate with good level of Microsoft Excel and Word.
* Some knowledge of GMP with the pharmaceutical industry would be an advantage.
* Understanding of validation requirements within the pharmaceutical industry.
Skills and Competencies
* Strong analytical skills and creative approach to problem solving.
* Strong communication and interpersonal skills to develop relationships with colleagues throughout all levels of the organisation.
* Excellent attention to detail, and ability to work with a high level of accuracy and precision.
* Curiosity in the field of probiotics with the desire to enhance knowledge.
* Must be confident in producing a high standard of report writing.
Our Offer
* Challenging tasks, short decision-making processes and a high level of personal responsibility in a modern work environment with flexible work time models.
* Room for innovative thinking and growth with the possibility to manage your own career path.
#IncludingYou
Diversity, equity, inclusion and belonging are cornerstones of ADM’s efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together.
For more information regarding our efforts to advance Diversity, Equity, Inclusion & Belonging, please visit our website here: Culture, Engagement & Inclusion | ADM.
About ADM
At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We’re a global leader in human and animal nutrition and the world’s premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at www.adm.com.
Req/Job ID
104888BR
Ref ID
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