Multiple Manufacturing / Quality Roles

We have multiple Manufacturing / Quality Roles at our clients located outside of Boston.

Quality Control Manager – Must have 10-12 years of molecular experience (PCR, & RT-PCR amplification and molecular genetic analysis). Should have a BS/MS and at least 6 years of working experience in a supervisory role in a GMP environment.

Continuous Process Improvement Analyst - Must have GMP and biomanufacturing experience. This is a must – otherwise resume will not be considered. Cell culture background is desirable and should have a BS/MS degree. 8+ years of operations management or consulting experience.

Training & Compliance / Quality & Manufacturing – This is a position for a person who has been in a Manufacturing role for several years and is looking to get into the Quality side. Should have a BS with 2-4 years of GMP Manufacturing experience

Clinical Lab Manager – Person should have 4-6 years of experience in a clinical setting. Med Tech Certification / CLIA lab experience is preferred.  Will be providing oversight to the PK/PD group

Manufacturing Supervisor – Must have 5+ years of Manufacturing and 2+ years in a leadership role. Must have cGMP cell culture operations experience.

Quality Control Manager - Will be managing QC Laboratory with testing of products and processes. Should have knowledge of FDA guidelines and roughly 7-10 years of experience with a BS degree (ideally Chemistry background)

These are all Direct Hire roles
If you do not have Manufacturing or Quality experience from a biotech or pharmaceutical company unfortunately we cannot consider you for these roles. They are a very specific need.

Local candidates only at this time