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Categories: Pharmaceutical, Production Support, Manufacturing/Production Skilled Trades
Employee will oversee all operations and staff employed by Almac Clinical Services in the packaging area ensuring that the quality of the products for the safety, well-being, and protection of the patient.
RESPONSIBILITIES: Allocating production operations to supervisors and teams, where possible, ensuring continuity throughout a study/protocol. Monitoring outputs and efficiencies thus ensuring that reject rates are kept to a minimum and job runs do not exceed the planned hours allocated. Identifying bottlenecks and problem areas within production with a view to putting corrective actions in place, or modifying procedures, to eliminate them. Maintaining the production schedule, ensuring resources are utilised in the most effective manner. Assisting with providing a breakdown of man-hours involved in each operation for costing purposes. Ensuring any calculators / mechanisms used for production planning are continually updated to reflect improvements or regular problems. Ensuring production analysis details are completed promptly and accurately as soon as possible after completion of operations. Create operations reports to capture the following performance indicators for production. Ensure no un-validated equipment is used within production. Enforce change control procedures within ALMAC CLINICAL SERVICES to ensure validation status is maintained. Take ownership of production SOPs and update as necessary to ensure all processes and procedures are covered. Responsible for the compilation and implementation of a structured training plan for all ALMAC CLINICAL SERVICES production staff. Ensuring Supervisors and coordinators deliver training in accordance with the plan and update records as required. Monitor staff levels and proactively recruit to cover anticipated shortfalls and to ensure annual financial targets are met.
**Coverage for 2nd shift & partial 3rd shift-candidate must be able to be flexible with hours - Monday- Thursday 4:15pm - 1:30am, Friday 3:45pm - 11:45pm
Requirements:
Bachelors Degree required. Degree in Manufacturing Management preferred. Must have (5+ years) Management/Supervisory experience. Must have clinical supply management experience. Must have personnel training and Production Planning experience. Working with a recognized quality system. Attention to detail. Ability to foster teamwork. Formal report/procedure writing. Interpersonal sensitivity. Quality oriented approach. Clarity and accuracy in verbal and written communication. Thorough knowledge of cGMPs. Ability to review and evaluate large volumes of information. Ability to manage project resources and timescales. Ability to work to a consistently high standard when under pressure. Familiar with Microsoft family of software. Ability to work flexible hours as tasks/timelines demand (weekend and shift work). Ability to travel preferred.
*Please include salary requirements upon resume submission.
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