Qc Salary at Bionostics Inc BETA

IMMEDIATE HIRE - cGMP QC STABILITY PROGRAM SPECIALIST How does it sound to be part of a groundbreaking Biotechnology company pioneering in harnessing the power of mRNA technology creating innovative medicines and vaccines? We're looking for a detail-oriented and proactive Stability Documentation Specialist to oversee data readiness and document management across our global stability team. In this dynamic role, you'll play a key part in coordinating critical stability documentation, collaborating with QC stability and cross-functional teams, and ensuring adherence to GMP guidelines and regulatory commitments. APPLY TODAY. Location: Norwood, MA. Shift: M - F, 1st shift. Pay Rate: $45 - $50/hour (based on qualifications and experience). What you will be doing: In this role, you will oversee data readiness and document management for the global stability team, focusing on timely submission and coordination of stability documentation. You'll collaborate with stakeholders to ensure GMP compl

Company Overview Meridian Adhesives Group is a rapidly growing, full service global adhesive solutions provider, specializing in adhesive technologies used in electronics, industrial, and infrastructure applications. Fueled by a series of strategic acquisitions since its formation in 2018, Meridian has established itself as an adhesive technology leader for a broad, global, blue-chip customer base comprised of OEMs, distributors, and industrial clients with an expanding global footprint. Job Summary As a Quality Control technician, you'll be responsible for making sure our products pass all of our internal standards. Duties & Responsibilities Test and review raw materials / finished products using a wide range of analytical instruments. Document test results and report abnormalities With general supervision and direction, operate and calibrate equipment. Performs other related duties as assigned. Skills & Abilities Excellent organizational and communication skills with attention to det

Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health. We are seeking a highly motivated and team-oriented professional with entrepreneurial spirit to join our company! This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today's cutting-edge research into tomorrow's breakthrough therapies. We are seeking a highly motivated and team-oriented Scientist, with Quality Control Bioanalytics focus, to join our second

WHO WE ARE RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science. THE ROSLINCT WAY Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE · Author, review, approval, and final authorizatio

Job Description Job Description Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve. Associate I, Quality Control (Microbiology, Environmental Monitoring) NOTES: Reason for Need: We are going into the commissioning and qualification of this facility so it’s a critical point in time for this site. BS Degree with at least 1-2 years of experience -OR- 5 years of cGMP experience minimum. Must have experience with strong environmental monitoring and compressed gas testing experience. Cleanroom experience Must be experienced with environmental monitoring, critical utility sampling, and gowning. Must have industry - pharma or biotech Main bulk of the position with be conducting environmental monitoring so the candidate must be enthusiastic about this. Willingness to learn, able to work in a fast-paced environmen

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

**Quality Control Associate II, Analytical** 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 stem cell an

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The QC Scientist - Critical Reagents is responsible for overseeing all reference standards and other critical reagents in line with internal SOPs and ICH guidelines. This individu