Job Description
Are you ready to take charge of antigen and vaccine manufacturing at our Milton Keynes site? As the Production IPT Lead, you'll play a crucial role in our Senior Leadership Team, ensuring our operations meet the highest GMP standards and align with company policies.
What you will do:
Drive Compliance:
Ensure strict adherence to safety and quality regulations while managing manufacturing processes to meet GMP requirements and audit standards.
Lead with Impact:
Own the success of the Production IPT by overseeing people, safety, quality, delivery, and cost.
Plan Strategically: Accountable for finite scheduling of production activities, schedule adherence as well as downtime tracking to drive problem solving and avoid repeated downtime for the same issue.
Accountable for the proactive supply risk assessment through use of site and enterprise risk assessment methodologies for all aspects of supply.
Develop Talent:
Accountable for the strategic development of first line leaders to ensure these leaders are equipped with the right support, tools, and competencies to effectively lead their team and drive the value stream.
Embrace Continuous Improvement through MPS tools:
Foster a culture of innovation and continuous improvement, driving productivity and customer satisfaction at all levels.
Safety First:
Promote a robust safety culture within your team, ensuring compliance with all EHS guidelines and conducting regular Gemba walk-throughs.
Quality Assurance:
Champion GMP compliance by promptly addressing deviations and implementing innovative solutions to complex challenges.
What We’re Looking For: A proven leader with significant industry experience, including experience in ERP, SAP, or MRP environments.
Minimum of 10 years of experience in the pharma industry including manufacturing operations experience.
Strong background in large-scale bacterial fermentation and downstream processing.
Expertise in change management, technical oversight, and risk management.
Possess excellent communication skills, and the ability to lead, inspire, and influence at all levels across the site and promote sustainable empowerment through transparent team communications.
Demonstrated ability to lead both direct and indirect reports fostering effective collaboration and achieving business objectives.
Demonstrated application of culture and business change methodologies (CEM, Inclusion, and BCCM) when realizing site and cross-functional process improvement initiatives.
Ready to make a difference? Join us and lead the way in shaping the future of vaccine production! We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply
HERE Current Contingent Workers apply
HERE Employee Status:
Regular Job Posting End Date:
02/13/2025 Requisition ID:
R329765
#J-18808-Ljbffr
Ensure strict adherence to safety and quality regulations while managing manufacturing processes to meet GMP requirements and audit standards.
Lead with Impact:
Own the success of the Production IPT by overseeing people, safety, quality, delivery, and cost.
Plan Strategically: Accountable for finite scheduling of production activities, schedule adherence as well as downtime tracking to drive problem solving and avoid repeated downtime for the same issue.
Accountable for the proactive supply risk assessment through use of site and enterprise risk assessment methodologies for all aspects of supply.
Develop Talent:
Accountable for the strategic development of first line leaders to ensure these leaders are equipped with the right support, tools, and competencies to effectively lead their team and drive the value stream.
Embrace Continuous Improvement through MPS tools:
Foster a culture of innovation and continuous improvement, driving productivity and customer satisfaction at all levels.
Safety First:
Promote a robust safety culture within your team, ensuring compliance with all EHS guidelines and conducting regular Gemba walk-throughs.
Quality Assurance:
Champion GMP compliance by promptly addressing deviations and implementing innovative solutions to complex challenges.
What We’re Looking For: A proven leader with significant industry experience, including experience in ERP, SAP, or MRP environments.
Minimum of 10 years of experience in the pharma industry including manufacturing operations experience.
Strong background in large-scale bacterial fermentation and downstream processing.
Expertise in change management, technical oversight, and risk management.
Possess excellent communication skills, and the ability to lead, inspire, and influence at all levels across the site and promote sustainable empowerment through transparent team communications.
Demonstrated ability to lead both direct and indirect reports fostering effective collaboration and achieving business objectives.
Demonstrated application of culture and business change methodologies (CEM, Inclusion, and BCCM) when realizing site and cross-functional process improvement initiatives.
Ready to make a difference? Join us and lead the way in shaping the future of vaccine production! We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply
HERE Current Contingent Workers apply
HERE Employee Status:
Regular Job Posting End Date:
02/13/2025 Requisition ID:
R329765
#J-18808-Ljbffr
