Senior Associate | Biopharma Process Scientist | Regulatory Specialist@ Lachman Consultant Services
Ireland
Joe Brady, PhD
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University of Dundee
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FlashIntel GPTJoe Brady, PhD is a highly experienced professional with over 34 years of work experience in the pharmaceutical, biopharmaceutical, blood-plasma proteins, vaccines, and medical device industries. He has worked in various countries including Ireland, Singapore, Netherlands, Belgium, France, and the USA. Joe specializes in validation, GMP, and quality systems. He has a strong background in upstream processing, formulation, fill-finish, and aseptic processing, as well as technology transfer and process scale-up. Joe is also skilled in risk management, GMP facility design, and computer system validation. He is a certified trainer and has expertise in competency-based training.
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About
Over 21-years combined project and operational experience in the pharmaceutical, biopharmaceutical, blood-plasma proteins and medical device industries in Ireland, Singapore, Netherlands, Belgium, France and the USA. Specialties and subjects of interest include: * Biopharmaceuticals, blood-plasma proteins, vaccines and biosimilars * Upstream & downstream processing, formulation & fill-finish, and aseptic processing * Technology transfer, process scale-up and new product introduction * Process validation * Risk management * GMP facility design and site layout * Computer system validation (GAMP®5, GAMP Guidance, ERP, SAP, MES, Serialisation) * Cleaning validation, and extractables and leachables studies * Primary and secondary pharmaceutical manufacturing, and medical device manufacturing * Lean validation * Certified trainer: highly experienced in competency based training
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Senior Associate | Biopharma Process Scientist | Regulatory Specialist
Pharmaceutical Manufacturing
Joe Brady, PhD's Professional Milestones
- Scientist: Downstream Processing, Tech Transfer And Process Validation (2018-01-01~2018-08-01): Streamlining the processing of digital content, optimized workflows, and enhanced process validation efficiency.
- Pharmaceutical And Medical Device - Project Engineering (2005-05-01~2013-11-01): Developing efficient processes to deliver high-quality pharmaceutical and medical devices, optimizing team collaboration and minimizing costs.
Education
Skill
Validation
Gmp
Pharmaceutical Industry
Biotechnology
Quality System
Biopharmaceuticals
Technology Transfer
V&v
Quality Assurance
21 Cfr Part 11
Medical Devices
Chromatography
Fda
R&d
Laboratory
Chemistry
Change Control
Computer System Validation
Distance Learning
Microbiology
Quality Control
Manufacturing
Training And Development
Sop
Higher Education
Adult Education
Testing
U.s. Food And Drug Administration
Pharmaceuticals
Employee Training
Automation
Verification And Validation
Capa
Analytical Chemistry
Lecturing
Standard Operating Procedure
Research And Development
Corrective And Preventive Action
Regulatory Requirements
Process Validation
Cleaning Validation
Training
Risk Management
Biosimilars
Certification
Colleagues
Linda Evans O'connor
vice president at lachman consultant services
Lou Da Silva
President | Global Pharmaceutical Compliance
Frances Marie Zipp
President | Chief Executive Officer
Jim Davidson
Vice President
Roy Sturgeon
President
Other Named Joe Brady, PhD
Frequently asked questions
We found 4 Joe Brady, PhD's email addresses
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Joe Brady, PhD works for Lachman Consultant Services
Joe Brady, PhD's role in Lachman Consultant Services is Senior Associate | Biopharma Process Scientist | Regulatory Specialist
Joe Brady, PhD works in the industry of Pharmaceutical Manufacturing
Joe Brady, PhD's colleagues are Linda Evans O'connor,Lou Da Silva,Frances Marie Zipp
Joe Brady, PhD's latest job experience is Senior Associate | Biopharma Process Scientist | Regulatory Specialist at Lachman Consultant Services
Joe Brady, PhD's latest education in University of Dundee
