Call us at: 877-463-7823
Why Join our Team?

QuaDPharma, Inc. provides a working environment where a team attitude drives the delivery of a quality experience both for the employee and the customer. Contact us today to find out how you can fit into the QuaD puzzle.

Employee Perks

Perks for a job could be measured in parking spaces, bonuses, time off, etc… But, when you join QuaDPharma's team you get more than a job. You get the opportunity to collaborate with clients who are innovating tomorrow's therapies for a wide range of life altering diseases. Even better, you get to work side by side with a motivated and energetic staff that has fun everyday they come to work. Our culture is our #1 perk. Come grow with us.

Join Our Team Of Experts

Project Manager

Part Time/Full Time - Interact with customers (Internal and External) to coordinate and drive implementation and routine operation of customer manufacturing and analytical testing projects. Candidate must be familiar with Good Manufacturing Practices (GMP) in a pharmaceutical environment. Candidate must posses excellent customer relations and communication skills

Bulk Formulator/Packaging Specialist, Manufacturing Operations

Part Time/Full Time - Work with customers (Internal and External) to conduct product formulation and equipment cleaning operations following approved batch records. Work with customers (Internal and External) to conduct product packaging and equipment cleaning operations following approved packaging work orders. Ensure all cGMP policies and procedures are followed and enforced in the manufacturing and packaging areas...

Associate Scientist/Scientist/Senior Scientist, Quality Control Microbiology

Part Time/Full Time - Conduct routine microbiological analysis of pharmaceutical raw materials, bulk formulated product, finished goods and environmental monitoring. Practical understanding of United States Pharmacopeia microbiology analytical techniques (Microbial Enumeration, Antimicrobial Effectiveness, Sterility). Candidate must be familiar with Good Manufacturing Practices (GMP) in a pharmaceutical laboratory environment...

Associate Scientist/Scientist/Senior Scientist, Quality Control Chemistry

Part Time/Full Time - Conduct routine laboratory analysis of pharmaceutical raw materials, bulk formulated product and finished goods. Practical understanding of United States Pharmacopeia chemistry analytical techniques. Candidate must be familiar with Good Manufacturing Practices (GMP) in a pharmaceutical laboratory environment...

Services

Semi-solids Manufacturing Liquids Manufacturing Gels Manufacturing Powders Manufacturing Capsule manufacturing Tablet Manufacturing Protein Manufacturing Biopharmaceutical Manufacturing Pharmaceutical Manufacturing Gene Sequencing Vector Preparation Expression System Selection Cell Bank Creation Cell Bank Management Biofermentation Process Development Purification Method Development Clinical Supply Manufacturing Solid Dosage Manufacturing ISO 8 Manufacturing ISO 7 Manufacturing USP/EP Raw Material Testing HPLC UPLC UV Detection Photodiode Array Detection Fluorescence Detection Gas Chromatography Thin Layer Chromatography Capsule/Tablet Dissolution Testing Water Content Viscosity Microbiological Enumeration Testing FT-IR Identification Testing Stability Services Quality Consulting Services
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11342 Main Street Clarence, NY 14031