Sr. Associate Manufacturing - Shift Role (FTC)

at  Amgen

JOB SUMMARY:

• Support the Manufacturing Manager in leading a shift of Process Technicians to achieve production targets efficiently in line with GMP, safety and other regulatory standards in an assigned process area.
• Ensure shift Process Technicians are given clear direction and information to perform daily tasks as per the production schedule.
• Lead an assigned process area Work Centre Team (WCT) to ensure cross functional alignment on objectives and action plans.
• Ensure the manufacturing schedule is accurate and up to date reflecting current status of production and clearly plan out all critical path activities for assigned process area.
• Foster a good safety culture in our team and act as a safety role model
• Be responsible for compiling, maintaining, and reviewing all necessary reports, documentation batch records/ EBRs relevant to the manufacturing area including use of relevant software systems and standard operating procedures.
• Proactively identify training needs for their manufacturing shift and facilitate completion of training to meet the area resource and cross training models.
• Assist, plan and implement continuous improvement ideas / opportunities using lean principles.
• Be proactive in the identification of process related issues including escalation & follow up for effective resolution to minimise impact on the manufacturing schedule.
• Contribute and assist with corporate, FDA, HPRA and other regulatory bodies during company audits.
• Takes the lead on the 24/7 shift team in the absence of the Manufacturing Manager

BASIC REQUIREMENTS:

• Educated to degree level or equivalent in a scientific or engineering discipline
• Must have relevant aseptic experience within a manufacturing function in a sterile pharmaceutical manufacturing or similar environment
• Be results-oriented with excellent organizational, communicational and team development skills with an ability to successfully interact with people, create a team environment and generate co-operation.
• Strong understanding of the quality system requirements and regulations for working in an aseptic drug product facility and ability to communicate those requirements to the manufacturing team.
• Demonstrated ability to deliver to team, site and personal objectives.

Please refer the Job description for details