ProStaff Workforce Solutions is seeking a Process Development Scientist I for a leading pharmaceutical company in Billerica, MA 01821. Our client specializes in radiopharmaceuticals, analytical methods development, and the production of parenteral drugs. If you are qualified, we would be excited to connect and discuss this opportunity further.
Full-time Onsite Pay Rate: DoE
1st shift
Job Summary Provides support for new product formulation, aseptic & topical process development, process transfers and troubleshooting existing manufacturing processes.
Area Of Responsibility
Work with production to support the transfer of manufacturing processes
Provide support for new product formulation and process development, including lyophilization development and process transfer into manufacturing
Execute laboratory experiments
Assist with investigations of established manufacturing procedures
Draft scientific experimental plans and protocols, execute and document experiments
Perform data analysis, prepare reports and other documents as needed
Provide investigational support of established manufacturing procedures
Prepare protocols, SOPs, technical reports and other cGMP documents
Work under supervision using standard and safe laboratory practices and procedures
Work with external contractors to obtain new equipment, technology or solutions for experimental plans
Other duties as assigned
Work Conditions:
Laboratory, fume hood, warehouse and office areas
Exposure to noise, hazardous and nonhazardous chemicals and waste
Must wear protective clothing in lab - lab coat, safety glasses and gloves
Physical Requirements:
Periodic use of repetitive motion
Stand, sit, use hands and fingers to handle or feel, reach with hands and arms, talk, and hear
Close and color vision; depth perception, ability to adjust focus
Lift up to 10 lbs.
Travel Estimate: Up to 5%
Qualifications
BS in related scientific major
Minimum 3 years related experience preferably in a pharmaceutical / biotech industry
Experience with techniques such as chromatography, lyophilization, formulation, sterile filtration, and process validation
Practical knowledge of chemical engineering principles, quality by design, and project management
Experience with aseptic techniques in a clean room environment
Experience working in a cGMP environment
Excellent verbal, written and interpersonal communications skills
Working knowledge of online collaboration tools, such as Sharepoint, Google Workspace, etc.
Ability to write technical reports to document outcomes of experimental plans
Ability to work independently and as a member of a cross functional team
Attention to detail and ability to manage multiple assignments concurrently