Manager, Quality Assurance Salary at Hindley BETA

**Job Title** Janitorial Account Manager **Job Description Summary** The Janitorial Manager Quality assurance will ensure our services are delivered and operations run smoothly and generate a consistent output that meet quality and efficiency standards. The Janitorial QA manager understands the Operations and the customer's needs, and possesses the detailed requirements for the account contract and KPIs. This position coordinates communications between management and the cleaning team and will include responsibilities for transitioning or transforming an account. The Janitorial Manager must have excellent communication and listening skills, with strong observational, analytical, and problem-solving skills. It is a requirement of this position to be proficient in Microsoft Office suite, and specifically PowerPoint. **Job Description** **Janitorial Manager - Quality Assurance Responsibilities:** + Gaining an understanding of the client's needs and requirements and communicating them and

Opening for Quality Assurance (QA) Manager About PhAST. PhAST is a venture-backed clinical stage AI healthcare technology company developing computer vision technology for rapidly diagnosing antibiotic resistance. Our in vitro diagnostic (IVD) platform provides clinical decision support for doctors, workflow improvement for hospitals, and helps accelerate the drug development process for pharmaceutical companies. Company headquarters are located in the biotech innovation hub of Boston (USA), with two international offices in Zurich (Switzerland) and Seoul (South Korea). This opening is for a position in the Boston, Massachusetts headquarters. Job Description. PhAST is seeking a Quality Assurance (QA) Manager. The successful candidate will be responsible for obtaining certifications, managing operations, and continuous improvement of PhAST’s Quality Management System (QMS) as PhAST completes the product life cycle and further develops additional in vitro diagnostic assays and platforms

Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. For the exponentially curious, Pall is a place you can thrive and amplify your impact on the world. Pall is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. Are you ready to put all your skills to use and lead in a manufacturing environment with several diverse value streams? The Manager of Quality Assurance is responsible f

Quality Assurance (QA) Specialist Job Category: Consulting Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: Continental US * * * What you'll get to do: Serves as a Quality Assurance (QA) Specialist who will be responsible for activities associated with delivery of customer-defined systems and software projects; basic responsibilities include: Develop, evaluate, and implement quality management processes and standards to ensure compliance with organizational standards and governmental regulatory requirements; work with customer quality management representatives to seamlessly design, integrate, and implement quality assurance practices to support achievement of program and customer goals and objectives. Develop and implement a Quality Control Program. Conduct quality audits and implement preventive/corrective actions. Document validation procedures and technical reports; assist with establish

QA Manager Permanent opportunity Onsite Managing a team of technicians, inspectors and engineers (10 direct reports) CMM understanding no programming necessary Lead quality improvement to optimize manufacturing processes and reduce cost. Train employees on quality procedures, standards and implementing process control measures for variability and defects. Develop and maintaining comprehensive QMS and ISO9001 a must. Conduct regular inspections and audits of production processes to identify quality issues and NCR's. Collaborate with production teams to identify any quality risks. 50% customer interfacing, working with customers to discuss quality issues. Bachelor's degree in engineering, quality management, or a related field. Proven experience in quality management roles within a manufacturing environment. Expertise in quality control methodologies, statistical process control (SPC), and data analysis. Strong understanding of industry standards and regulations related to product qualit

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resourc

Job Description The Manager position is an integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor qualification, internal systems and document audits to ensure compliance with cGCPs. The CQA Manager supports the department initiatives by leading CQA projects and assists with management of department resources. This position must be able to quickly identify critical and high risk business and compliance issues and report immediately to CQA management and assist/lead investigations and/or corrections of such issues. This position reports to the Associate Director of Clinical Quality Assurance. Responsibilities Schedule, conduct and/or supervise Good Clinical Practice (GCP) audit services by an external vendor/consultant and/or internal resources (auditors) which will support Clinical Development activities including but not limited to: Audits of clinical vendors, clinical

Date Posted: 04/22/2025 Hiring Organization: Rose International Position Number: 481599 Job Title: Electrical Engineer Job Location: Foxboro, MA, USA, 02035 Work Model: Hybrid Employment Type: Temporary Estimated Duration (In months): 8 Min Hourly Rate ($): 50.00 Max Hourly Rate ($): 52.00 Must Have Skills/Attributes: Documentation, MS Excel, MS Office, Project Management, Quality Assurance Job Description Required Education: • 4 Year bachelor’s degree in electrical or Electronic Engineering. Required Qualifications: • Good understanding of control electronic Products, specifically analog and digital circuits, and power electronics circuits with 5+ years of experience. • Ability to lead PCB specs release in qualification and in PDM. • Support qualification of electronic components such as IGBTs, Magnetics, Thyristors, AC/DC capacitors, FAN’s, etc. • Knowledge of test equipment, CRO, AC Source, DC Source, Auto transformers, Multimeters, Data loggers. • Ability to design and implement PC