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

龍沙（中國）投資有限公司成立于2003年9月，是瑞士龍沙集團(tuán)全資在廣州設(shè)立的投資性公司。公司旨在于醫(yī)藥、化工及生命科學(xué)領(lǐng)域進(jìn)行投資和再投資，同時(shí)提供以下服務(wù)：

-協(xié)助或代理龍沙所投資企業(yè)的貨物及設(shè)備采購業(yè)務(wù)，并在國內(nèi)外市場銷售他們的產(chǎn)品；

-為龍沙所投資企業(yè)提供售后服務(wù)、技術(shù)支持及人力資源服務(wù)；

-為投資者提供咨詢服務(wù)并為龍沙的關(guān)聯(lián)公司提供市場信息、投資政策等咨詢服務(wù)。