Qc Salary at Osram Gmbh BETA

Company Description Pharma Job Description W2 candidates only - No CTC allowed Skills Needed - A280, CE-SDS, icIEF, ELISA, SoloVPE, qPCR. The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activites. Also participate in quality testing for customer in-process, final product testing and stability studies when needed. •Applies job skills and company's policies and procedures to complete a variety of tasks. •Running test samples for In-Process, Lot Release and Stability studies. •Running test samples for (but not limited to) investigations, transfers and validations. •Reviewing assays •Training others •Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods •Projects - such as method transfers, new instruments, method qualifications •Use of Microsoft Suites (Word, Excel, PowerPoint) •Use of Laboratory computer systems •Potential p

**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 . **Position Summary** Responsible for supporting QC testing for

Job Description Job Description Company: Large Pharmaceutical Company Title: Technical Writer Contract Position: 6 months with potential extension Location: Lexington, MA - on site. Description: Primary duties are non-laboratory support of the QC analytical methods functions in method validation and method transfer projects. Primary activities would generally include but not limited to Authoring analytical method and support documentation for QC release and stability testing of biologics. Authoring method validation protocol and reports to support technology transfers. Creation, review, and revision of comprehensive method validation protocol, reports, , ensuring accuracy and adherence to ICH, FDA, EMA, regulatory standards. SPECIFIC QC FOCUS AREA Analytical Methodologies for potency, impurities, content, and identity attributes in biologics (recombinant proteins, antibodies, ADCs, fusion proteins, enzymes, etc.). (i.e.: cell based assays, residual ProteinA, host cell protein, residual

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza AG is continually growing and evolving, offering dedicated individuals' opportunities to join our team! We are currently in search of a QA Specialist 3, QA Enabling Functions to support our Quality Assurance team in New Hampshire, USA. This role plays a vital part in our dedication to delivering elite products and services. We value teamwork and innovation, and our QA team is pivotal in ensuring our processes are detailed and align with regulatory standards. Key responsibilities: Perform QA on the floor reviews for the Quality Control (QC) laboratory at the

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

Job Description Job Description TRI-K Industries, Inc. has been a leading provider of sustainable specialty ingredients since 1974. Our mission is to inspire consumer brands and enable their success by delivering differentiating technologies, prioritizing product efficacy and sustainability. Motivated by our core values of Empathy, Curiosity, and Excellence, our customers and partners get the attention, agility, and innovation they need to be successful in the marketplace. We specialize in proteins, including amino acids and natural peptides, modern preservatives, and multi-active, multi-functional ingredient solutions. Our in-house development team continually pioneers new materials, differentiating our customers’ brands. We strive to amplify consumers’ voices within our organization, ensuring we bring relevant offerings and innovations to the market. The QC Laboratory Technician will be responsible for conducting routine and non-routine analyses of raw materials, in-process samples,

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 The QC Analyst II, Flow Cytometry & Molecular Team