to join our renowned multinational corporation, with over a 60-year legacy in pharmaceutical innovation. Based in Taiwan, they are steadfast in their dedication to maintaining regulatory compliance and upholding the highest standards of product quality, thus contributing to the advancement of global healthcare. Apply now to be part of their mission-driven team and make a profound impact on healthcare worldwide.
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We are currently seeking a Plant Director (OSD) to join our renowned multinational corporation, with over a 60-year legacy in pharmaceutical innovation. Based in Taiwan, they are steadfast in their dedication to maintaining regulatory compliance and upholding the highest standards of product quality, thus contributing to the advancement of global healthcare. Apply now to be part of their mission-driven team and make a profound impact on healthcare worldwide.
is responsible for the overall production activities in accordance with their quality specifications and strict adherence to GMP rules within the required time and established production costs.
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Responsible for providing oversight for Quality on-the-floor and operations support, the QA Associate will support manufacturing operations and IPC testing through purposeful presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations. Required to perform a 12-hour shift (full night shift preferably).
Responsible for providing oversight for Quality on-the-floor and operations support, the QA Associate will support manufacturing operations and IPC testing through purposeful presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations. Required to perform a 12-hour shift (full night shift preferably).
Responsibilities:
Support the maturation and continuous improvement of site quality systems, including On-the-floor quality oversight, deviation management, change control and ensure that the systems are managed in compliance with cGMP expectations
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The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule.
Responsibilities:
Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system)
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Drive significant market share and growth for our client's established branded product portfolio by developing and executing innovative marketing strategies.
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Our client is a global biopharmaceutical company that develops and market advanced therapies that address some of the world’s most complex and serious diseases.
As the Business Unit Head, you will be entrusted with the strategic leadership and management of their primary care and specialty care portfolio in Singapore.
Pharmaceuticals & Medical Devices (Healthcare & Medical)
Our client is a global biopharmaceutical company that develops and market advanced therapies that address some of the world’s most complex and serious diseases.
As the Business Unit Head, you will be entrusted with the strategic leadership and management of their primary care and specialty care portfolio in Singapore.
Key responsibilities include:
Develop and implement comprehensive business strategies to maximize market penetration, capitalize on growth opportunities, and maintain a competitive edge in the pharmaceutical market.
Take ownership of the profit and loss for the business unit, driving revenue growth and profitability in alignment with corporate objectives.
Lead and inspire a diverse team of sales and marketing professionals, fostering a culture of excellence, collaboration, and continuous improvement.
Conduct thorough market analysis and stay abreast of industry trends, competitor activities, and regulatory developments to inform strategic decision-making and optimize business performance.
Build and maintain key customer relationships, including payers, patients, regulatory authorities and key opinion leaders.
Requirements:
Bachelor's degree in Business Administration or related field
Minimum of 5-8 years of progressive leadership experience in the pharmaceutical industry, with a proven track record of success in managing P&L, leading sales and marketing teams, and driving business growth in Singapore
Exceptional leadership, communication, and interpersonal skills, with the ability to inspire and motivate teams towards achieving strategic objectives
How to Apply:
Interested applicants may apply by submitting an updated CV for a confidential discussion.
Consultant: Henry Zheng
Registration Number: R1106964
EA License Number: 17C8502
Company information
Registration No.
201634573Z
EA No.
17C8502
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