Caring for the world, one person at a time, inspires and unites the people of Johnson & Johnson. We embrace innovation—bringing ideas, products and services to life to advance the health and well-being of people around the world. We believe in collaboration, and that has led to breakthrough after breakthrough, from medical miracles that have changed lives, to the simple consumer products that make every day a little better. Our over 125,000 employees in 60 countries are united in a common mission: To help people everywhere live longer, healthier, happier lives.
Post : Associate Scientist, Drug Product Development
Job Description
• Designing and optimizing various formulation and filling unit technical operations including freeze/thaw, mixing, sterile filtration, vial and syringe filling and lyophilization
• Participate in the execution of pilot to scale fill/finish manufacturing processes.
• Design and manage non-GMP stability studies on experimental and target formulations
• Perform studies that contribute to the continuous improvement manufacturing process, and administration equipment used to support clinical dosing
• Perform technical analysis of the project data, including trending of data, and may be expected to present data to peers and functional management
• Author technical reports and make presentations of technical data
• Follow general laboratory safety procedures, as related to biologically-derived materials
• Collaborate with contacts inside the company including functional line management as well as scientists in related functional areas such as Research and Development, QC/QA, Clinical, Manufacturing, Toxicology, and Regulatory (CMC)
• Perform her/his duties consistent with good laboratory practices
Candidate Profile
• B.S. in an appropriate scientific discipline with at least 2 years of related laboratory experience OR an M.S. with at least 1 year laboratory experience is required
• Pharmaceutical and/or Chemical Engineering experience is preferred
• Demonstrated experience with formulation and fill/finish process development for therapeutic protein and/or biologic products is preferred
• Working knowledge of GLP and GMP requirements are preferred
• Experience in continuous improvement as it relates to manufacturing and drug product development is preferred
• Experience with aseptic process procedures, compliance and operational technology of various dosage forms is preferred
Additional Information:
Experience: 2 years
Qualification: B.S, M.S
Location: Pennsylvania-Malvern
Functional Area: Quality Control
Industry Type: Pharma
End Date: 30th April, 2018
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