Expert Profile
Steven Laurenz
Principal Consultant, BioPhia Consulting Inc
Expertise: Over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. Skilled in taking new products from early laboratory stage to successful manufacturing launch. Expert in integrating Quality by Design and risk management into product development. Experience in establishing a Quality System for a R&D Quality Assurance organization.
Experience: Headed product development departments at Abbott Laboratories and AbbVie Inc. Leadership positions in numerous technical consortium.
Other: Black Belt certified in Business Excellence and Master Certificate in Applied Statistics
Trainings by Expert
Understanding and Implementing a Quality by Design (QbD) Program
Category:
Drugs and Chemicals (Pharma)
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GXP Pharmaceutical
,
Quality and Safety
,
Audits & Inspections
,
Supply Chain and Manufacturing
,
Drug Development
,
Drugs Regulations
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
Understanding and Implementing a Technology Transfer Process
Category:
Drugs and Chemicals (Pharma)
,
Biotechnology
,
Quality and Safety
,
Supply Chain and Manufacturing
,
Drug Development
,
Quality & Safety
,
Drugs Regulations
,
Biotech Regulations
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
QA/QC
Implementing a Modern Pharmaceutical Quality System
Category:
Drugs and Chemicals (Pharma)
,
Risk Management
,
All FDA Regulated Industry
,
GXP Pharmaceutical
,
Quality and Safety
,
Supply Chain and Manufacturing
,
Drug Development
,
Drugs Regulations
,
Audit & Inspection-Role
,
Quality Audit
,
All FDA Reg. based Audit
,
Drugs Inspections
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Common FDA Regulations
,
QA/QC
Practical Implementation of Pharmaceutical Quality Risk Management (QRM)
Category:
Drugs and Chemicals (Pharma)
