Supervisor, QC Salary at Cytiva Inc BETA

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Bristol-Myers Squibb in Devens, MA, is seeking a remarkable Man

**Technical BioPharma Manufacturing MSAT Engineer MA-TC** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com . **Astellas Institute for Regenerative Medicine (AIRM)** is a wholly-owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of

Adecco Staffing is assisting a Medical Device Manufacturing facility in Chelmsford MA with their needs for Quality Control Inspectors on 1st and 2nd shift! This is a temp-to-hire opportunity. **Hours -** **1st shift** 5:00am-1:30pm **2nd Shift** 1:00pm-9:30pm **Pay -** **1st shift** $22hr **2nd Shift** $ 24.20hr **JOB SUMMARY:** With limited supervision performs quality inspections for IAB-C. Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in Principal Responsibilities. **RESPONSIBILITIES/DUTIES:** + Compliance to all work instructions, Quality regulations, SOPs, WIs, GMPs and GDPs in the effort to manufacture high quality medical devices at all times. + Training: As required, will train employees to inspection requirements and techniques in manufacturing or other areas. + Retrieval of documentation or work instructions through Agile as necessary, to perform inspections. + Reviews orders and job packets, recording batch numbers and quantiti

Job Description Job Description A Central Massachusetts manufacturing company is currently seeking an Operations Manager to join our team in Shrewsbury, MA. Position Overview: The company is a major manufacturer of fiberglass reinforcements to the Abrasives Industry. The company’s coating, cutting and kitting capabilities expands its customer base to assist the Military, Defense and Public Safety, Automotive and Medical Industries. The Operations Manager is responsible for overseeing all aspects of the business including production, new equipment/equipment maintenance, quality, and purchasing and to coordinate with the company’s customer service and accounting functions. The Operations Manager is expected to be directly involved with key customer accounts and reports directly to the President of the Company. In this role, you will: Ensure the overall delivery, productivity, and quality of the unit's offerings on a daily basis and develop strategies for improvement Identify and resolve

Job Description Job Description Job Summary: The Quality Control Manager is responsible for overseeing all aspects of the quality control function to ensure product quality and compliance with industry regulations. This includes developing and implementing quality control systems and coordinating with other departments to achieve company quality objectives. Key Responsibilities: Product Testing: Oversee the testing of products to detect any defects or deviations from specifications. Ensure all products meet regulatory standards and quality benchmarks. Acting ISO-9001 Management Representative Prepare and present quality reports to senior management. Continuous Improvement: Identify opportunities for continuous improvement in the QC process. Qualifications: Bachelor’s degree in technical field. Minimum of 3 years’ experience in a quality control role within a manufacturing environment. Strong knowledge of quality control standards and testing methodologies. Strong problem-solving abilit

Company Overview: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE™ platform, Dyne is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. For more information, please visit https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook. Role Summary: The Manager, Quality Control will support and oversee stability programs as well as QC testing and release of antibody drug conjugates and intermediates. This role will also contribute to the management of analytical development and QC activities in Phase 1 through BLA and commercial production. These acti

Quality Control Analyst II - Analytical Position Summary: Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder

Our client, a leader in the pharmaceutical industry, is seeking a Pharmaceutical QA Specialist to join their team. As a QA Specialist, you will be part of the Quality Assurance department supporting various manufacturing teams. The ideal candidate will have strong communication skills, a proactive mindset, and the ability to work collaboratively, which will align successfully in the organization. Job Title: Pharmaceutical QA Specialist Location: Cambridge, MA Pay Range: $50-55 per hour What's the Job? Execute all activities following quality and regulatory standards and procedures. Provide on-the-floor support to manufacturing activities. Review manufacturing batch records for completeness and compliance with cGMPs. Ownership of the following quality systems: Change Control, CAPAs, Deviations, and Self inspection auditing, QA reporting and approval of GMP documentation. Review and approve Standard Operating Procedures, logbooks and QC data. Assist in the coordination of work for the QA