心血管和移植事业部-医学信息沟通代表-衡阳
Wuhan, China Fixed Term Posted on Jan. 24, 2025 Closing on Feb. 28, 2025About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Main Responsibilities
TheCareer Conversion Programme (CCP) (Train-and-Place)for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand. This programme is jointly supported by the Workforce Singapore (WSG) and Workforce Advancement Federation (WAF).
The training programme consists of 15 months of local attachment at Sanofi (Aventis-Pharma). Only candidates eligible for CCP programme may apply.
Updating the site validation master plan and procedures related to ALCM and CPV of GXP lab equipment.
Support periodic analytical method control trend review/ investigation and data evaluation on method performance, recommend method improvements where appropriate.
Support the life cycle management of the QC lab equipment i.e qualification of QC equipment and periodic review are maintained for their intended use.
Maintaining up to date the lab equipment inventory.
Participate in proper documentation issuance and review of qualification and maintenance deliverables, such as risk assessments, traceability matrices, protocols, reports, deviations, and summary reports.
Support laboratory qualification Investigation and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs.
Providing support during regulatory inspections and audits.
Prepare metrics and monitoring data for the qualification and validation activities, to identify trends and issues, during life cycle management of QC laboratory equipment.
Support initiatives for continuous improvement in QC support processes related to lab equipment management in coordination with QC excellence team.
Perform periodic analytical method control trend review/ investigation and data evaluation on method performance, recommend method improvements where appropriate.
Support invalid assay trending program in the QC laboratory.
Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements.
Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks.
About You
Minimum of two (2) years of experience in quality control in GMP environment with hands-on exposure and theoretical requirement of QC laboratory instruments and ALCM management.
Bachelor’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology
Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
Experienced in analytical method continuous monitoring requirements.
Strong interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.
Independent, discipline and assertiveness in decision-making and execution in laboratory activities.
Continuous improvement mindset.
Must be highly motivated and able to work well as team player.
Location: Incumbent will be based in 61 Gul Circle Singapore 629585
Pursue progress. Discover extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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Sanofi careers in China
From research and engineering to sales, we're all working toward the same ambitious goal – halving the time from discovery to therapy. Our people develop incredible careers, alongside 40 new innovative drugs and vaccines for China. We also support the national health department in preparing for China 2030. It's how we've become a China Top Employer and have continued to grow since opening our first China site in 1982.
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