QC Analyst II Salary at Charm Sciences Inc BETA

CONTRACT MUST HAVES: 2+ years' GMP, pharmaceutical, and/or QC raw material testing experience Experience with QC raw material sampling Experience with technical and GMP investigational writing and testing models Knowledge of Raw Material analytical techniques- such as FTIR, UV-Vis, Osmolality, pH, NIR, Raman, Potentiometric titration Position Summary This position reports to the Associate Director, Quality Control Raw Materials, and will work with others in Quality Control, Analytical Development teams, Quality Assurance, Manufacturing and CROs to support routine QC testing for Raw Materials for the manufacturing of Gene therapy products. The Analyst will specifically support the Raw material and gene therapy program pipeline (as needed) including but not limited to Project Management of the raw material program and development of testing strategies. Responsibilities: Perform routine sampling, testing, and review of GMP data, used for release of raw materials as needed to support Manuf

*W2 Only Overview: The Analyst IV is responsible for ensuring quality and compliance standards are met to support the commercialization of pharmaceutical/biotech programs. This role ensures completeness, consistency, and accuracy of regulatory filings, laboratory data, and reports through thorough review processes. This position offers remote flexibility with occasional on-site presence in Norton, MA, and Cambridge, MA, and potential travel to CMO/CTL sites. Key Responsibilities: Verify integrity and traceability of regulatory dossier sections against reference methods and reports. Review analytical data for accuracy, completeness, and correct entries, including electronic data and laboratory documentation (notebooks, worksheets, logbooks). Ensure complex notebooks for analytical method validation, verification, and transfer testing are compliant with approved protocols. Audit electronic data trails to confirm adherence to applicable procedures. Resolve data discrepancies with clients

Immediate need for a talented Quality Control Analyst II. This is a 10+ Months Contract opportunity with long-term potential and is located in Framingham, MA(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:25-58235 Pay Range: $35 - $41/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Perform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. Aid in the development of test methods. Conduct data review and preliminary evaluation of results. Solve p

**Job Description** The finance organization is a trusted business partner delivering information and innovative solutions for decision-making in order to deliver quality products and capabilities to our customers and, ultimately, the warfighter. We are committed to employee growth and development allowing employees to build a long term career at BAE Systems. In addition to challenging day to day assignments, employees are encouraged to pursue special projects, participate in formal and informal mentoring programs and networking events, and rotate into different roles with increasing levels of responsibility. BAE Systems also provides employees with opportunities to engage with and positively impact the internal and external community in which we work. **Job Description, & Essential Duties & Responsibilities:** Project finance plans, controls, and reports program performance relating to cost and schedule according to the Earned Value Management System. Project finance is a well-rounded

GMP QC Analyst III - Contract - Lexington, MA Proclinical is seeking a dedicated GMP QC Analyst III to join our client's team in Lexington, MA. Primary Responsibilities: The successful candidate will be instrumental in maintaining high standards of quality and compliance from development through commercialization. You will perform both routine and non-routine testing, participate in data trending, and support laboratory operations. Your contributions will be vital in method transfers, qualifications, and validations, ensuring the efficiency and effectiveness of our Quality Control functions. Skills & Requirements: Degree in chemistry, biology, biochemistry, or related field. Experience in GMP Quality Control within the pharmaceutical/biotech industry. Knowledge of method transfer and analytical method implementation. Strong technical writing skills, especially for investigations. Proficient in data analysis with attention to detail. Problem-solving skills and experience with CAPA. Stro

Job Description Job Description Job Description We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services. We are seeking entry-level experienced personnel or fresh graduate students willing to be trained as per our client's requirement and able to relocate. Most of our openings require 3-4 days' onsite presence at the client site. Minimum Qualification: 0-3 years of experience in life science (pharmaceutical, biology, chemistry, bioinformatics) or engineering industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or supply chain. Minimum bachelor’s degree in the above concentration. Valid US work authorization. Virtually able to participate in our training program. Able to relocate anywhere in the US. About White Collar Technologies Inc. is one of the fastes

Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 Months Pay Range: $28.00 to $33.00 Job Description: The Quality Control Technical Transfer Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. 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 of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Responsibilities: 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 f

Job Description Job Description Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Control professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Quality Control Management at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve. POSITION SUMMARY The Senior Quality Control (QC) Analyst is responsible for performing routine and non-routine assays of in-process samples, finished drug product (DP), and stability samples within the QC laboratory in accordance with SOPs for product release and validation. This role also participates in special projects, method development/transfers and cleaning study q