Veranova

The Production Technician is responsible for the safe, cost effective, and timely manufacture of product that is fit for intended use and meets customer requirements and production schedule. This position is 100% on site at Devens, MA facility and will follow a rotating shift 6PM-6AM schedule. Core Responsibilities:Promote a positive work environment by maintaining a safe work area and ...read more

The Separation Scientist I is responsible for the use of chromatographic techniques to support the chemical process development and GMP manufacturing of Active Pharmaceutical Ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget. The role requires an in-depth understanding of instrumentation and techniques ...read more

The Associate Director is responsible for people and project management as part of the Site Leadership Team as well as the development and optimization of synthetic routes of active pharmaceutical ingredients (APIs) to deliver projects on target for quantity, quality, time, and budget. Core Responsibilities:                                                                                         ...read more

The Production Lead is responsible for operating production equipment, completing associated documentation, and directing production technicians on shift on the same duties. The production lead is also responsible for ensuring that the shift meets all safety, compliance, and performance goals while meeting production schedules. The position will coordinate with other departments such as QA, QC, ...read more

The Sr Manager, QA is responsible for leading the Veranova Quality Assurance team, managing quality oversight of the manufacturing process and associated operations. This includes leading and managing multiple QA teams for batch record review, batch disposition, and on the floor QA support to ensure GMP compliance across all stages of manufacturing, as well as disposition and release of starting ...read more

The Analytical Scientist is responsible for the development and implementation of analytical procedures and specifications in support of the development and manufacture of active pharmaceutical ingredients (APIs) for traditional synthetic molecules (including potent) and peptides. Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (LC-MS, GC-MS, NMR, ...read more

The Associate Scientist II, ARD is responsible for development and implementation of analytical procedures and specifications in support of the development and manufacture of active pharmaceutical ingredients (APIs) for traditional synthetic molecules (including potent) and peptides. Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (NMR, ICP-MS, FTIR and ...read more

The Senior Project Manager will lead cross-functional project teams to deliver complex CDMO (Contract Development and Manufacturing Organization) programs. This role is responsible for managing R&D and manufacturing activities, including seamless technology transfers between internal and client manufacturing sites. Serving as the primary point of contact for the client, the Senior Project ...read more

The Senior Maintenance Technician is a hands-on position whose duties include assisting with repairing, maintaining, adjusting, calibrating and installing equipment to ensure proper operations. In addition, activities related to facility upkeep and activities related to maintaining the two sites in good working order. Core Responsibilities:Contributes to production flow by minimizing downtime due ...read more

The QC Analyst II will perform laboratory analysis and sampling of raw materials, intermediates, finished products, cleaning verification samples, stability samples and other miscellaneous samples following relevant SOP’s while adhering to current Good Manufacturing Practices (cGMP) to ensure they meet the required quality standards and specifications. This role also involves basic maintenance ...read more

Under the direction of a Production Supervisor, the Kilo Chemist II works on manufacturing Active Pharmaceutical Ingredients (APIs) in support of the business unit while meeting local, state, and federal quality and safety regulations. This role is 100% on site at our Devens, MA facility and will work a rotating shift schedule on all shifts. Core Responsibilities:Completes batch records in ...read more