Qc Salary at Kavlico Corp BETA

Job Description Job Description A global Pharmaceutical company that harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases. Making a positive difference in the world is at the heart of what we do. Join us to make a difference!! Essential: Experience as business process owner Ability to problem solve and troubleshoot system issues Ability to work independently and deliver right first time results Knowledge of data integrity requirements of QC systems Ability to prioritize appropriately based on criticality Strong, clear, concise communication skills Document authoring and review capabilities Preferred: Ex

Duties: Performs technical review of proposed electrical plans and specifications submitted by District personnel, consultant staff, or commissioned architects and engineers for construction projects Provides review comments regarding adherence to District standards, quality of development and documentation of electrical design, coordination with other disciplines, and other technical issues as required. Provides comments, lessons learned and research to support the development and maintenance of the District's Design Guidelines including the School Design Guide, Educational Specifications, Guide Technical Specifications, and Standard Technical Drawings for the Facilities Services Division. Provides comments and lessons learned to update and maintain District policies and guides for the design of educational facilities and/or District construction electrical specifications to assure conformance to building codes and safety requirements and to improve the quality and economy of construc

Job Title: Quality Analyst Job Description We are seeking a detail-oriented QC Analyst to join our team. The role involves testing using PCR and SDS-Page, validating assays, managing change controls, conducting stability and raw material testing, and maintaining thorough documentation. The QC Analyst will also oversee a team of 4-6 people and provide team leadership. Hard Skills + Validating assays + Method Development + Testing using PCR + Testing using SDS-Page + Managing change controls + Stability testing + Raw material testing + Documentation Soft Skills + Team leadership + Attention to detail + Strong communication skills Work Site This is a fully on-site position in Los Angeles, California. Work Environment Working in an office and lab setting About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, inno

Who We Are HMC Architects is an employee-owned design firm with a desire to make a difference in our communities. As a purpose-driven firm based on values, our mission to design for good drives everything we do. And our ownership culture creates alignment and increased commitment to that mission, keeping us on track to being successful. What We Do Founded with the purpose of anticipating community needs, HMC aims to create designs that have a positive impact, now and into the future. We focus primarily on opportunities to have the most direct contribution to communities-through healthcare, education, and civic spaces. This position is located in Los Angeles, California. The position requires 3 days in the office and the ability to work from home Mondays and Fridays. Summary The Senior QA|QC Architect will be responsible for reviewing contract documents in accordance with applicable codes, HMC standards, and industry best practices. Document reviews should identify errors, omissions, in

Job Title: QC Research Associate Location: Santa Monica CA Duration: 06 Months Description: All of previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and reports. Evaluates equipment for purchase and performs installations and qualifications of the new instruments. Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Pra

Overview: Join FUJIFILM Diosynth Biotechnologies in our new facility location - Thousand Oaks, California! The Specialist, Quality Control supports Fujifilm Diosynth Biotechnologies California (FDBC) QC with the business analysis, design, development, implementation, validation, and support of existing and new Laboratory Information Management Systems (Labware LIMS) and other lab applications. The Specialist, Quality Control is a customer facing role, working in close collaboration with Quality Control (QC), Quality Assurance, Manufacturing, and Information Technology (IT) teams. The Specialist will follow FDBC methodologies for systems and project governance, leverage tools & techniques to capture business and functional requirements and use approved corporate documentation templates and systems for software development lifecycle documentation. External US: Position Summary: The Specialist, Quality Control supports Fujifilm Diosynth Biotechnologies California (FDBC) QC with the busine

Only Local Candidates or someone based in California: Top 3 Must Have Skill Sets: 1. QC background 2. Experience with HPLC, GC, KF 3. Bachelor's degree with 3 years experience, or master degree in analytical chemistry 4. Preferred to have empower or electronic notebook Analytical Chemistry role is a 100% onsite, lab-based position, supporting the oligonucleotide (oligo) program with a focus on synthetic small molecules. The ideal candidate holds a Master’s degree in Analytical Chemistry (preferred) or a Bachelor’s with 2-3 years of relevant experience, with hands-on expertise in LC, GC, KF, and proficiency in Empower software. Responsibilities include sample testing, impurity standard management, and chromatography support. Local candidates only. In this role, you will integrate and optimally utilize platform and in-depth product attribute knowledge to advance client products and ensure success through pivotal clinical phases to marketing authorization application. Key Responsibilities

Description OVERHILL FARMS INC. JOB DESCRIPTION CLASSIFICATION: Quality Systems Manager EFFECTIVE DATE: 09/09/2024 REPORTS TO: VP of Quality Assurance & Food Safety DEPARTMENT: Quality EXEMPT/NON-EXEMPT: Exempt Overhill Farms is a leading custom manufacturer of high quality prepared frozen foods, serving customers in the branded retail, private label and foodservice sectors. We provide a one-stop solution that offers new product development or precise replication of existing recipes as well as product manufacturing and packaging. Our custom product lines include poultry, meat and fish specialties, pastas, soups, sauces, certified organic and vegetarian offerings. These can be prepared as entres, plated meals or bulk-packed meal components. Overhill Farms: A custom manufacturer of high-quality frozen food products POSITION SUMMARY: The Quality Systems Manager is responsible for leading and managing the administration of documents and audits required to qualify ingredients and suppliers.