BioPharma Consulting JAD Group provides a complete portfolio of technical support and solutions for the FDA regulated industry. We deliver solutions with a flexible cost effective approach to meet your company’s needs. BPC JAD group is a company created to help our customers bridge the gap between their business strategy and results. Our mission is to help our clients succeed by partnering with them and providing value added business solutions on the validation, engineering and compliance fields. We will carry out our mission by creating a long-term partnership with our customers and provide reliable and cost effective technical solutions. BPC JAD Group objective is to deliver reliable tailored solutions; from providing consultation to becoming part of your staff. We will develop customized frameworks to help our customers unlock the hidden value in their plants, facilities, equipment and people with an optimal integration of resources regulations and technology.
Open Positions
Project Mgr
Doctorate OR Masters + 2 years of Project Management experience OR Bachelors + 4 years of Project Management experience OR Associates + 8 years of Project Management or High school/GED + 10 years of Project Management
Specialist Quality Control
Doctorate or equivalent experience, with strong technical writing, communication, and project management skills
DRY-EM TS/MS (Technical Services / Manufacturing Science) Scientist.
3+ years experience in spray dry and/or solid dosage manufacturing, strong regulatory knowledge, and effective communication skills
Sr Engineer
Pharmaceutical/biotech manufacturing knowledge, problem-solving and analytical skills, technical writing and presentation skills, project management and leadership skills
Cleaning Validation Engineer
Bachelor's degree, experience in cleaning validation, knowledge of GMP regulations
Quality Control Analyst II
Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific discipline and 4–8 years of pharmaceutical or biotech experience in a GMP QC environment
Manufacturing Contractor I
Biotech Certificate or Associate's degree, 1+ year of industry experience, 0–3 years of manufacturing experience
Manufacturing Engineer-Medical Device
Bachelor's degree in Engineering or Biomedical Engineering, 1+ year of professional experience in Medical Device Manufacturing
QA Associate, Quality Operations
2 years of GMP experience, Bachelor’s degree in a scientific or engineering discipline, hands-on GMP experience
Deviation Investigator
5+ years of experience, Bachelor's degree, Strong analytical and communication skills