Quality Control Salary at Meyer Design Inc BETA

Job Description Job Description Job Title: Quality Control Inspector II Pay Rate: $22.00-$31.00/hr. Location: Newark, DE 19702 Duration: One-Year Contract (extension/conversion possible) Shift: M-F 7:00AM to 4:00PM Summary: Perform inspections, check testing and sampling procedures for product manufacturing processes. Carries out packaging line, manufacturing inspections and sampling and testing of incoming components and raw materials to ensure that company standards are met. Responsible for reviewing and release of Device History Records. Monitors critical equipment and instrumentation. May assist with validating or troubleshooting testing methods, including assays. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated. Experience Preferred Minimum Non-Technical Degree: 1-2 Years Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial. Previous quality assurance or manufacturing experience is beneficial. Experienc

Description Bristol Bay Construction Holdings LLC (BBCH) is seeking an experienced dual hat Quality Control Manager/Site Safety and Health Officer to join our SES Civil and Environmental team, a subsidiary of BBCH. The primary responsibilities of this position are to coordinate, plan, and supervise subcontractors and/or craft activities to ensure adherence to plans and specifications; enforce site safety and provide contractor quality control. Candidates must have strong organizational and communication skills. This position is located in Folsom, Pennsylvania (Philadelphia area). Pay Range $100,000 - $130,000 DOE Project Scope of Work: Interior and exterior renovation of the Folsom Marine Corps Reserve Center including site work, finishes, MEPs, and roofing. We are an equal-opportunity employer. All applicants will receive consideration for employment, without regard to race, color, religion, creed, national origin, gender, or gender identity, age, marital status, sexual orientation, v

JOB DESCRIPTION One of our large industrial chemical manufacturing clients is seeking a QC Team Lead to join their Quality team in Philadelphia, PA. This role will be reporting directly to the QC Supervisor, ensuring that all products meet the required quality standards and specifications. Responsibilities include but are not limited to: Generating COA's, troubleshooting lab equipment, updating and reviewing procedures and must possess strong lab skills (wet analysis, ion exchange, titration). REQUIRED SKILLS AND EXPERIENCE - Bach Degree in Science or Engineering discipline - 3+ years hands on QC experience - Leadership experience NICE TO HAVE SKILLS AND EXPERIENCE - ISO9001 - Experience with analytical lab equipment Compensation: $30-40/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DC

Job Description Job Description Quality Control Specialist Location: Boyertown, PA | Pay: $18-$20/hr | Full-Time | Mid-Shift| Benefits: Medical, Dental, Vision, Paid Time Off, Retirement, Life Insurance --- Join a company where quality and precision matter—because our customers depend on it. At Berk International, we know that delivering high-quality products starts with our people. We’re looking for a Quality Control Specialist who takes pride in their work and enjoys a fast-paced, team-oriented environment. Your attention to detail will help ensure our customers receive the reliable products they need. If you have quality control or production experience, we want to hear from you. --- Schedule & Pay · Mon-Fri 1:30pm - 10:00 pm · Training Required on 1st Shift · Competitive hourly pay based on experience --- What You’ll Do · Conduct quality checks on raw materials, in-process production, and finished products to ensure compliance with standards. · Identify and document quality issues,

Shift: Wed. - Sat. 7:00am - 6:00pm Essential Functions and Responsibilities Performs deviation investigations for all areas within Quality Control Perform out of specification investigations with an emphasis on QC analytical assays (flow cytometry, ELISA, and other cell-based assays) and microbiology assays Work cross-functionally to create relevant corrective/preventative actions (CAPA). Support maintenance of a database in support of QC metrics and KPl's. Revise quality documents in support of deviation mitigation and/or CAPAs Support programs to improve on-time closure rates for all quality records. Other responsibilities as determined. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) 1-3 years of experience in the biopharmaceutical industry within a cGMP Quality Control role Basic knowledge of biological drug development with respect to Quality Control Extremely detail-oriented with strong analytical, written,

Quality Control Specialist needed! The Quality Control Specialist II, Sterility Assurance will have substantial experience leading QC sterility assurance program(s) in a Pharmaceutical or Biotechnology environment. The Quality Control Specialist II, Sterility Assurance is a key support role and reports to the Manager, QC Sterility Assurance. Essential Functions and Responsibilities: Assist with the development of sterility assurance principles at the site in the areas of aseptic processing, and contamination control. Support the site compliance to the global microbial control standards/procedures on environmental monitoring, critical utilities, contamination control strategy, clean-room management, microbiological methods and validations, sterilization and aseptic processing controls, disinfectant efficacy studies and microbial risk assessments. Assist with the design of the contamination control strategy. Develop microbial contamination/Cross contamination risk assessments (HACCP/FMEA

Quality Control Specialist needed! Overview: The Quality Control Specialist II – Sample Management will ensure time-sensitive distribution of quality control samples in support of QC-related activities. They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all of the cell therapy asset. The weekend position is either a Sunday to Wednesday or Wednesday to Saturday shift with a 9am-7pm schedule. Essential Functions and Responsibilities: Manage all aspects of QC sample logistics for raw material, in-process, and final product samples including sample storage, sample inventory and reconciliation, scheduling, and shipping in LIMS based system. Maintain sample integrity by ensuring that all samples are managed (i.e., stored; handled; shipped) in compliance with procedures, specifications, and cGMP Provide timely distribution of samples internally and externally to testing

Compensation & Details: 2 Openings Fully onsite role in Malvern, PA - in the laboratory $34-$38/hr - exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law 10 PTO Days & 6 Sick Days 12 month extending contract Requirements: Minimum two (2) years of relevant work experience Experience in Medical Device, Biopharmaceutical, or Pharmaceutical industry Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) Must have experience in the following: qPCR, cell culture, Flow Cytometry, and