QA Assistant Salary at Cocokids Inc BETA

Job Description Job Description Company Description Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in bioanalytical and CMC analytical services for biotech and pharmaceutical companies developing biologics. Our expertise spans a wide range of therapeutic modalities, supporting projects from discovery through clinical development. Role Description Reporting directly to the CEO, the Director of Quality Assurance (QA) will be responsible for the development, management, and continuous improvement of quality systems ensuring compliance with Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and other applicable regulatory standards for our bioanalytical GLP lab in Pleasanton, California. This role ensures that facilities, equipment, personnel, and procedures meet all regulatory requirements and effectively supports nonclinical and clinica

Must have experience testing native iOS apps in a client/server environment.Experience with the following tools is required: Charles Proxy Xcode/iOS Simulator Radar Central Station Confluence/Connectme iPad & iPhone - Mobile Apps testing Duties include Mobile App features testing, Write test plan, test cases, test cases execution, write test reportWork closely with Development engineer and Project manager. The resource must be available for special event deployments that can run overnight and being onsite for these events. Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Manager of Clinical Quality Assurance position is an exciting opportunity to build upon solid clinical r

Responsibilities: Excellent understanding of Quality Management Systems (QMS) and regulatory requirements in the medical device industry. Strong problem-solving skills with a focus on root cause analysis, CAPA, and continuous improvement. Ability to work collaboratively with cross-functional teams and communicate effectively at all levels of the organization. Proficient in the use of quality tools such as Six Sigma, PFMEA, and statistical process control (SPC). Requirements: Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or similar certifications. Minimum of 4-6 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation protocol and other relevant medical device standards. Experience with process validation, risk management, CAPA, RFA, and validation protocols in a manufacturing environment.

Are you a detail-oriented professional with a passion for quality assurance and compliance in the pharmaceutical or biotechnology industry? Adecco is seeking a **_Quality Assurance (QA) Associate_** to join their clients team in **_Concord, CA_** . **_Job Opportunity: Quality Assurance Associate $20.00/HR + Benefits_** **_Location: Concord, CA_** **_Why work with Adecco:_** + **_Pay is $_** 25.00/HR. (20.00/HR.) + **_Benefits, including health, dental, vision, and 401k._** **_What youll do:_** Ensure compliance with data integrity standards under **21 CFR Part 11, 210, and 211** . Maintain and manage **QA files, training matrices** , and other essential records. Review **Certificates of Analysis** , raw data files, in-house documentation, and logbooks for accuracy and completeness. Scan, submit, and archive data and certificates to clients efficiently. Manage **document control** and participate in **quality event investigations** using **eQMS MasterControl** . Provide support for **cl

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perfor

At Eko, we're dedicated to providing healthcare professionals with industry leading digital tools to hear and understand their patients' hearts and lungs. With our platform, clinicians can detect cardiopulmonary disease with higher accuracy, diagnose with more confidence, manage treatment effectively, and ultimately give their patients the best care possible. With over $165M in funding from partners like 3M and the Mayo Clinic, Eko has become one of the fastest growing digital health companies, doubling our customer base in the last year to over 500,000 clinicians across 4,000 U.S. hospitals. We've built a tremendously talented, diverse, and mission driven team and are proud to be certified as a Great Place to Work®. Together we are committed to investing in each other and our mission to ensure all patients have access to high quality care. Reporting to the Senior Director of Technical Operations & Quality, The Head of Quality Assurance is responsible for overseeing all quality assuran

At Bellota Labs, we are a fast-paced, hypergrowth startup poised to revolutionize the gaming world with ClubWPT Gold-a groundbreaking product from the World Poker Tour. Driven by innovation, game integrity, and exceptional customer experiences, we are on a mission to set new standards in online gaming. We are now looking for a Senior Quality Assurance to join our team, playing a critical role in ensuring the quality, performance, and reliability of our platform. If you are passionate about cutting-edge technology and building robust, scalable systems, this is your chance to shape the future of online gaming with us! Key Responsibilities: Test Strategy and Planning: Design, implement, and maintain comprehensive test plans and test cases for functional, integration, regression, and performance testing, tailored for gaming experiences. Collaborate with stakeholders to define quality requirements for upcoming features and releases, aligning with the expectations of a gaming audience. Lead