Facilitator Leominster, MA, USA Req #2826 Wednesday, April 10, 2024 Location Outpatient Treatment facility in Leominster, MA Schedule Part time, 5 hours a week Pay rate $25.00 $30.00/hour Qualifications LADC I or CADAC certification preferred. Certification for IPAEP preferred. Minimum of a high school diploma or equivalent and a minimum of one year of supervised counseli

This position requires strict adherence to current Good Manufacturing Practices (cGMP), established cleaning practices and procedures, and compliance with quality standards and regulations. The purpose of the sanitization program is to control microbial contamination and to serve as a corrective action for the loss of control for viable excursion contamination. Standard O

The Senior Manager, Quality Analytical Microbiology is an advanced technical resource in the principles and application of microbiology quality assurance and compliance. The Senior Manager, Quality Analytical Microbiology coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects. Key Duties and Responsibil

The Director, GCP Compliance is responsible for the escalation and management and compliance activities in support Quality Issues Management and other activities within RDQA. This role will act as a lead for GCP related events and escalation of these events. This individual will work closely with Quality Leads, Study team members, and other pillars in the Quality organiza

The Vendor Quality Management Director provides technical and strategic leadership for vendor quality, vendor quality processes, and associated governance for the cell and gene therapy business unit. This position focuses not just on the "what" but the "how", ensuring phase appropriate and risk based compliance. This is a hybrid role located in our Seaport offices. Key Du

Under the direction of the Principal Investigator or designee, the Supv. Lab Operations Ophthal is responsible for specified clinical and lab research activities in the Macular Degeneration Center of Excellence. This position is on iste in Worcester, MA. For additional information please visit www.umassmed.edu/seddonlab Responsibilities ESSENTIAL FUNCTIONS Responsible for

The Associate Director, Small Molecule CMC Compliance (Product Complaints and Recalls) is responsible for leading activities associated with the Product Complaint Quality System and Global Recall and Defect Notification Systems. This role will support quality activities associated with the Small Molecule CMC Compliance team and will partner with various internal and exter

The Sr. Director of Packaging and Labelling Operational Quality will advance compliance oversight for packaging and labelling validation, commercial supply, and product launches in North America and worldwide across the Small Molecule portfolio. The Sr. Director will have a broad role working with stakeholders across Manufacturing, Supply Chain and Regulatory. The role wi

Create a healthier, brighter future for pets, pet parents and people! If you want to make a real difference, create an exciting career path, feel welcome to be your whole self and nurture your wellbeing, Petco is the place for you. Our core values capture that spirit as we work to improve lives by doing what's right for pets, people and our planet. We love all pets like o

The GMP Quality Operations Director serves as a Quality leader in the areas of process validation, and equipment validation in oral solid dosage form. The Director is also responsible for managing multiple department activities with a high degree of independence while providing oversight of the development, implementation, and maintenance of relevant quality initiatives i

The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects , effectively ensuring alignment with corporate goals and compliance with all regulatory require

The Director, Cell & Gene Quality, International will support defining the strategy for the international expansion of Cell & Genetic programs. The role will establish the quality risk management plans, work closely with cross functional QA, CMC, External manufacturing, Supply Chain and Commercial teams to ensure QA oversight is maintained. Key activities include develop,

SERVICE As a member of the Patient Care Team, the Operations Manager is responsible for ensuring that the patient and family members are attended to in a professional manner. The Operations Manager is responsible for responding to the needs of the patient/family members in a timely manner and maintains a professional and friendly demeanor at all times. As a lead member of

S Env Svcs New Bedford , MA Support Services Pay Grade SC013 Full time , Evening Shift, every weekend. Holiday rotation , 3p 1130p Req # 74242 Work for One of the World's Best Hospitals! For Five Consecutive Years, Newsweek named Southcoast Health among the World's Best Hospitals (Charlton Memorial, St. Luke's, and Tobey). In addition, since 2018, Southcoast Health has be

The major responsibility of this position is to routinely produce the highest quality radiopharmaceuticals and radiotracers for human use on a regular basis with full regulatory compliance. This involves but is not limited to Collaboration Work with BICOR Director of Radiochemical R&D and project Principal Investigators to select potential compounds of interest Work with