Qc Salary at Qvc Inc BETA

Line of Business: Asphalt Pay Range: $73,570.00 – $98,193.33 About Us Heidelberg Materials is one of the world's largest suppliers of building materials. Heidelberg Materials North America operates over 450 locations across the U.S. and Canada with approximately 9,000 employees. What You'll Be Doing Oversee QC for 9 HMA plants Provide technical guidance and support to ~8 indirect reports Monitor/manage day to day compliance with specifications/targets Heavy engagement with QC Techs on testing, customer complaints, statistical tracking Perform hands-on lab work as required Must be available as required for nights/weekends Engage with Operations, Sales and Construction on product quality, bid specifications, etc. Annual update of state required PennDOT QC plans, also ensure compliance throughout year Oversite of daily DOT certifications Identify continuous improvement opportunities (product and yield optimization) Implementing required standards, processes in HM labs Implement corrective

Duties: 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 Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Minimum four to Five (4-5) years of experience in the pharmaceutical industry within a Quality Control Sterility Assurance role or Microbiology role\ Experience running or validating microbiology rapid safety methods (endotoxin, mycoplasma, and sterility). SME on 2-3 of the Rapid Safety assays

Duties: Oversee day to day operations in the QC Microbiology laboratory in support of environmental monitoring and batch related microbiology testing Oversee growth promotion testing of microbiological media u Ensure all in-process and lot release microbiology testing is performed and reviewed accurately and timely. Ensure timely review of routine environmental monitoring data, microbiology testing data, and excursions and OOS reports are completed accurately and timely. Support site qualification/validation/commissioning activities as needed. Qualifications: Bachelor’s degree in Biology, Microbiology or related scientific field is required Minimum five (5) years of experience in in a cGMP Quality Control microbiology role Prior experience in managing a team and having direct reports. High proficiency in aseptic techniques when executing microbial test methods and environmental monitoring Proficient in performing technical writing (e.g., test methods, SOP's, protocols, ) Pay Scale: $12

Job Description Job Description QC Environmental Monitoring Expert needed for a contract opportunity with Yoh Scientific’s client located in King of Prussia, PA. This position is in the production lab of a major pharmaceutical company and requires a minimum of a BS in biology/microbiology or related science field with extensive experience in environment monitoring in GMP area (minimum of 3-5 years of experience). Experience with endotoxin and bioburden testing required. Schedule: Monday – Friday, 1st shift. Key Responsibilities: Perform Environmental Monitoring in GMP Classified areas including viable air, non-viable air, surface sampling, and settling plate analysis. Prepare Environmental Monitoring samples for analysis Participate in laboratory investigations associated with Environmental Monitoring Enter data in appropriate GMP systems (LIMS/LES, Veeva, SAP/ERP) Complete necessary SOP and Hands-On training associated with Environmental Monitoring Qualifications: Education: Minimum o

Duties: Perform assay co-qualification, validation, and technical transfer of updated and new assays, as well as potential new products. Act as subject matter expert (SME) and train laboratory personnel on assays. Perform all activities with respect to GMP/GDP compliance. Author, review, and approve technical assay documents including but not limited to protocols, reports, and procedures. Support technical problem solving for issues pertaining to GMP Quality Control. Qualifications: Bachelor’s degree in Biology, Biochemistry, Microbiology, Chemistry, or related scientific field or equivalent combination of education and experience. Minimum three (3) years of GMP experience in the pharmaceutical industry within a Quality Control Solid understanding and functional knowledge with hands-on experience with two (2) or more of the following: Multicolor Flow Cytometry, Cell-based ELISA, cell culture with cell enumeration (NC-200) Experience in technical writing (e.g., technical reports, test m

QC Microbiology Manager - Permanent Position - Open to relocation No Third Party Inquiries Please Open to relocation Most urgent role is for night shift - Shift: Monday to Friday from 11:00pm to 7:30am Must be eligible to work in the US. Client does not allow Visas. Key experience: Microbiological and Environmental testing experience. Must have clean room experience and comfortable being suited for clean rooms (bioburden, endotoxin, gram stain) Cell therapy a must. Overview The Manager, Quality Control (QC) Microbiology, is responsible for oversight of day-to-day microbial QC operations at Cell Therapy Center (iCTC). The role will be responsible for working in a GMP- regulated environment and have good understanding of QC microbiology test methods and environmental monitoring. This role must be able to apply phase appropriate cGMPs and regulatory requirements in the product development life cycle, including but not limited to: lot release and stability testing, method qualification and

QC Scientist, Sterility Control - Permanent - Philadelphia, PA Proclinical is seeking a QC Scientist, Sterility Control. This role is responsible for assisting in the development and implementation of all microbial contamination control processes/procedures for the company's clinical and commercial programs at two manufacturing sites in Philadelphia. Primary Responsibilities: This role will effectively collaborate with multiple stakeholders to ensure the harmonized execution of contamination control policies across the two manufacturing sites in Philadelphia. This role will also support new product transfers related to contamination control aspects of manufacturing process and equipment design, microbial method validations and rapid microbial methods. Skills & Requirements: Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum four to Five (4-5) years of experience in the pharmaceutical industry within a Quality Control Sterility Assurance role or Micro

Marine QA /QC Coordinator required for a Shipyard Marine Quality Assurance/Quality Control Coordinator Philadelphia, PA The Marine QA/QC Coordinator will assist with installing and integrating Owner Furnished Equipment (OFE) on vessels, coordinating with the shipyard, subcontractors, and vendors. They will conduct periodic inspections to ensure ship construction meets standards and specifications. In the absence of the Communications Supervisor, they will handle administrative tasks like organizing meetings and documenting minutes. Additional responsibilities may include tasks related to the NSMV Program or other vessel construction projects. The Marine QA/QC Coordinator will have the following responsibilities: Ensure all work follows safety standards and protocols. Oversee QA/QC processes, identify and address construction quality issues, and conduct internal audits. Monitor the shipyard's audit program for quality oversight. Maintain accurate records of inspections, KPIs, non-confor