Product and Process Engineer
This is an exciting opportunity to join Haleon as a Product and Process Engineer.
About the Role
We are seeking a highly skilled and experienced engineer to coordinate, plan, and execute technical aspects of development/validation/transfer of manufacturing and packaging processes and equipment cleaning procedures.
Key Responsibilities:
* Technical coordination, planning, and execution of development/validation activities for manufacturing/packaging processes, including transfer of new products, improvement/maintenance of current processes, and qualification of new raw materials and packaging components.
* Preparation and review of documentation required for development/validation trials, including protocols/reports, operative instructions, sampling plans, control charts, master formulas, and production orders.
* Coordination and execution of development/validation activities for equipment cleaning procedures.
* Update of standard operating procedures (SOPs) regulating department activities in line with company guidelines and regulations.
* Collaboration and support for technical aspects with other plant functions, including QA, QC, Regulatory, Procurement, Engineering, for evaluation/preparation of documents such as change controls, master formulas, deviations, investigations, risk assessments, technical assessments, periodic product reviews (PPRs), user requirement functional specifications (URFS), and HACCP manuals.
* Collection and evaluation of process data (in-process control) and quality control analytical data for report preparation.
* Collaboration and support to production for technological issues in commercial productions.
* Technical support to operations and Opex for continuous improvements/simplification initiatives impacting performance, productivity, and loss reduction.
Background:
* Scientific university degree in chemistry, pharmacy, pharmaceutical technology, chemical engineering, biology, or biotechnology.
* 2-5 years of experience in a GxP pharmaceutical regulated environment.
* Experience with process validation of pharmaceutical and dietary supplement products, including different forms (coated/uncoated tablets, capsules, granules, creams) and packaging technologies (blisters, sachets, sticks, bottles, tubes).
* Familiarity with microbiological sampling and experience in validation of probiotics products would be a plus.
* Experience with cleaning validation of GMP production areas.
* Knowledge of statistical software (e.g., Statistica, Minitab).
* Good knowledge of written and spoken English.
* Strong relationship management skills, including the ability to work with inter-functional teams and in a matrix organization with multiple stakeholders' interface.