At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

高级生产工艺专员 

YOUR TASKS AND RESPONSIBILITIES

• Lead Cluster related products technical transfer under coach of Cluster Lead
• Lead technical knowledge transfer, incl. alignment with sending unit to get transfer documentation, complete gap analysis, identify validation plan and investment plan (if further investment is needed).
• Initiate and execute trial, qualification and validation to ensure related submission dossier is in place and with high quality.
• Ensure all technical knowledge established via GMP/HSE system (incl. SOP, training, etc.) before commercialize new product.
• Build-up line team capability to have deep understanding for new technical process, risk assessment, operation behavior etc.
• Maintain and improve work processes for cluster related products
• Support Cluster with regular based qualification and validation e.g. RQ, OPV, PQR etc.
• For change/project triggered qualification and validation. Responsible to determine qualification/validation strategy and plan, implement risk assessment and operation execution.
• Conduct process confirmation to ensure qualification and validation outputs e.g. GMP time limit, equipment status etc. are closely link to operation and well maintained.
• Assess and initiate work process optimizations and changes based on (SQDC) Loss analysis
• Coaches/Teach AO & PIPS standards & execution
• Lead work processes CL/CIL/CO management and execute process confirmation to ensure work process is "healthy".
• Coach line team to build-up problem-solving capability to enable team problem (incl. defect, deviation, event etc.) investigation and CAPA identification
• Coach line team with A3R Case study (5W1H, Fish bone, 3Why etc), to ensure the assessment & analysis is reasonable, logic and scientific based during deviations/events and changes.
• Float to lead shift handover dialogues within cluster. 

WHO YOU ARE

• Bachelor’s degree or above, in pharmaceutical or Chemistry. 3-5 years or above working experience in pharmaceutical or consumer health with strong GMP knowledge and practice.
• Familiar with cGMP, EP, GTA and FDA principle. Having new product introduction (NPI) working experiences in multinational company is preferred.
• Excellent co-create, coordinate, teamwork and communication skills.
• Fluent in Mandarin (orally and writing), good in English (oral and writing).
• Good defects finding and problem solving capability
• Familiar with semi-solid and liquid technology and manufacturing process.

YOUR APPLICATION

If your background and personal experience fit this profile, please send us your complete application at www.career.bayer.cn If you have any recommendations, please kindly send mail to cnreferral@bayer.com
 

Location:                   

China : Yun Nan : KunMing 

Division:

Consumer Health 

Reference Code:

831606