Veranova

The Maintenance and Facilities Supervisor oversees daily operations and performance of facilities and maintenance functions. This hands-on role includes managing routine maintenance and repairs for building systems, equipment, and infrastructure within the Pilot Plant—spanning HVAC, electrical, piping, and general facilities upkeep. The ideal candidate brings strong technical expertise and ...read more

We are seeking a Document Control Specialist to support the design, implementation, and maintenance of our Quality Assurance documentation system. This role manages the issuance, tracking, and control of GMP documents including SOPs, batch records, protocols, and reports, while administering quality documentation software. The ideal candidate will help ensure a compliant and well-maintained ...read more

The Training Specialist is responsible for designing, delivering, and managing training programs to help achieve the goal of providing outstanding education and training across the site.   Core Responsibilities:                                                                                                                   Develop, evaluate, and deliver high-quality training programs across ...read more

This position will lead material planning, with direct responsibility for developing and managing processes and monitoring operating strategies in collaboration with cross-functional business partners. Utilizing SAVIOM, Excel, and Veranova’s ERP system, this role will integrate production planning, capacity planning, and manufacturing scheduling for a portfolio of client-owned products. Core ...read more

This role is responsible for leading the Veranova Quality Systems & Compliance team. This role will oversee the compliance function and related processes for the multi-site New England region. The position manages and provides direction to Quality Systems and Compliance staff, ensuring that processes and activities are performed in compliance with company policies, procedures, standards and ...read more

The QA Deviations Associate will oversee the investigation, documentation, oversight, and resolution of deviations to ensure compliance with regulatory standards, internal policies, and industry best practices.  The ideal candidate will bring expertise in deviation investigations for CGMP manufacturing and testing, an understanding of chemical processes for intermediates and APIs, a proactive ...read more

This Contamination Control Specialist is the site SME responsible for coordinating all cleaning validation and verification activities related to intermediate and API manufacturing, including facility surfaces and equipment. This role involves close collaboration with various departments to ensure compliance with regulatory and customer requirements while implementing effective cleaning ...read more

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. Core Responsibilities: Completes batch records in accordance with FDA and Current Good Manufacturing Practices (cGMP) guidelines.Demonstrates technical proficiency and self-assuredness in applying cGMP ...read more

The Associate Director of Quality Assurance is responsible for leading the Veranova Quality Assurance team, managing quality oversight of the manufacturing process and 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 ...read more

The Senior QA Associate will perform on the floor walkthroughs of Manufacturing and Quality Control areas to drive Inspection Readiness activities. They will also perform review and release of Active Pharmaceutical Ingredients (APIs) in support of clinical and commercial product manufacturing, as well as assist in the development, implementation, and maintenance of quality systems and other ...read more

The Training & Development Manager is responsible for designing, delivering, and managing a robust New England training program across the departments and the sites to help achieve the goal of providing outstanding education and training across the organization.   Core Responsibilities:                                                                                                               ...read more

The Process Engineer is responsible for the evaluation, design and implementation of elements of new or improved processes as they are transferred from development to production. The Process Engineer is also responsible for the monitoring of manufacturing processes while providing production support and ensuring compliance with safety and quality standards.  Core Responsibilities:               ...read more

The QA Supervisor will coordinate with the Manager/Associate Director, Quality Assurance, the day-to-day activities of the Quality Assurance group in the support of the site’s Operations (manufacture, testing, shipment, etc.). This person will evaluate and implement systems, methods, techniques, and solutions to moderately complex quality and regulatory compliance issues, and be responsible for ...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

We are seeking a highly motivated and skilled Senior Scientist with experience in analyzing antibody drug conjugates (ADC) to join our ARD team in New England. The successful candidate will play a hands-on role in the development, qualification, transfer, and validation of analytical methods to support the development of ADC’s and other complex bioconjugates.  Core Responsibilities: Collaborate ...read more

The Production Lead's principal responsibilities include operating production equipment, completing associated documentation, and directing production technicians on shift on the same duties. The Production Lead is responsible for ensuring that the shift meets all safety, compliance, and performance goals while meeting production schedules. The position also coordinates with other departments ...read more

The Scientist I - Process Research & Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget. Core Responsibilities: Delivers experimental output with a high ...read more

The Scientist I - Process Research & Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget. Core Responsibilities: Delivers experimental output with a high ...read more

The Supplier Quality Assurance Specialist will evaluate, qualify and monitor the quality of external vendors providing Veranova materials, supplies and services impacting the quality of materials produced by Veranova. Core Responsibilities: Lead and perform supplier qualification activities including conducting audits, working with new and existing suppliers to help them understand Veranova’s ...read more