Key responsibilities:

?      Responsible for providing leadership and oversight to all routine operational and administrative activities which occur within the individual’s team.

?      Display superior process understanding & equipment troubleshooting ability under both routine & non-routine scenarios

?      Maintain currency of knowledge in emerging and advances of technologies

?      Attain subject matter expertise in ≥ 2 areas of manufacturing operations e.g. USP: Media Preparation & Primary Recovery, DSP: Column Packing & Bottling, SUP: Buffer Preparation & Dispensing,

?      Attain 100% trainer qualifications in identified areas of specialization

?      Able to assimilate quickly to leadership roles in other process areas outside of areas of specialization

?      Participate in Customer & Regulatory Audits

?      Follow through to completion Quality Tag-outs, Change Requests, Planned Deviations and/or Computer Systems Change Controls (CSCCs)

?      Recognized as a DELTAV system expert and competent in addressing and/ or reviewing Minor/ Major Deviations

?      Make real-time non-critical decisions on operational issues based on superior knowledge of defined SOPs & policies

?      Review more critical/ complex decisions with Manufacturing Management and/ or other support functions

?      Able to identify suite problems, troubleshoot, identify & complete or coordinate corrective action

?      Provide formal peer review to Snr/ Section Lead and Section Manager

?      Provide active mentoring/ coaching to Biotechnologists.

?      Plan and prioritize suite activities/ resource loading on a 2-week look-ahead of production schedule

?      Excellent coordination skill between departments for multiple parallel activities

?      Able to communicate manufacturing operations perspective effectively to management.

?      Highly motivated and is regarded as an upcoming leader both technically and in soft skills

?      Direct day-to-day manufacturing activities of team as required by Snr/ Section Lead and Section Manager

?      Able to manage multiple priorities and is recognized by colleagues as a source of expertise

?      Able to support MSAT, Lot Review and Deviation Investigation groups when situation calls for it

?      Act as responsible suite designee during technology transfers

?      Create & present training materials/ seminars on technical/ cGMP issues

?      Involved routinely in OE improvement projects and make recommendations to improve manufacturing processes

?      Own & lead process improvements projects (often complex in nature) in collaboration with MSAT/ Engineering 

Key requirements:

?      Have cell culture working experience in a biologics industry

?      Degree/Diploma in a related Science/Engineering discipline

?      Demonstrate commitment to cGMP, EHS compliance aspects of clean-room and production operation

?      Strong knowledge of Biopharmaceutical processing is an added asset

?      Excellent Knowledge of cGMP applications

?      Positive team oriented attitude

?      Good communication skills

?      Demonstrate leadership skills

?      Willing to perform rotating 12-hour shift pattern

龙沙（中国）投资有限公司成立于2003年9月，是瑞士龙沙集团全资在广州设立的投资性公司。公司旨在于医药、化工及生命科学领域进行投资和再投资，同时提供以下服务：

-协助或代理龙沙所投资企业的货物及设备采购业务，并在国内外市场销售他们的产品；

-为龙沙所投资企业提供售后服务、技术支持及人力资源服务；

-为投资者提供咨询服务并为龙沙的关联公司提供市场信息、投资政策等咨询服务。