Sign upLog in

Validation Coordinator

Integrated Resources, Inc

Billerica, Massachusetts

Apply
JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biology, Biotech and Pharmaceutical, Clinical Research, Communication Skills, Communications Protocols, Customer Support/Service, Documentation, Information Technology & Information Systems, Laboratory, Laboratory Testing, Logistics, Multitasking, Organizational Skills, Presentation/Verbal Skills, Problem Solving Skills, Procedure Development, Product Support, Project Planning, Project/Program Coordination, Project/Program Management, Quality Assurance, Quality Control, Record Keeping, Rehabilitation Nursing, Technical Consulting, Testing, Time Management, Validation Testing, Writing Skills
LOCATION
Billerica, Massachusetts
POSTED
2 days ago
Validation CoordinatorA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionSeeking a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions.Candidate is responsible for being the technical liaison for laboratory scale validation studies performed.The Validation Project Coordinator (VPC) is the "Study Director" responsible for the design, conduct, and reporting of the study results to the external Biopharmaceutical/Pharmaceutical customer.The VPC is responsible for project planning, timeline management, customer communication, as well as technical consultancy and guidance to adapt service scope to specific customer needs.As well as those listed above, the VPC is responsible for project logistics such as sample reception, protocols and reports communication, and the overall coordination of validation studies.The role of the position is to support client products in customer applications and to supply technical resource for the validation aspect of customer filtration processes.QualificationsBachelor's degree in biology or related science discipline with a 2-5 years of experience or a Master's degree with a 1-2 years of experience from Biotech/Biopharmaceutical industry.Must be able to work in a fast paced environment.Must be organized, neat, have good documentation skills and practices, and good project management skills.Excellent written and verbal communication skills and presentation skills.Excellent communication skills and the ability to work in team environment and possess the ability and skills to interface with various departments and customers.Ability to work with customers.Prior experience of QA/QC, validation and/or similar laboratory experience.Aptitude for initiating testing procedures and protocols and/or development of new methods.The ability to plan laboratory testing, solve problems, develop reasoning related to test results.Strong aptitude in laboratory skills with the ability to multitask and handle different projects/responsibilities simultaneously.Good record keeping abilities and computer/data skills.

About the Company

I

Integrated Resources, Inc