QC Specialist Salary at 8Biomed BETA

Line of Business: Aggregates 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 agg plants, Philadelphia portables, Downingtown recycle 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 stan

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

10 Days of PTO / 6 Sick Days / Paid Holidays Compensation: $35.76/hr to $45.87/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Required Skills & Experience -Minimum 2 years of relevant GMP work experience in a lab setting -Minimum 1 year of experience working with mammalian cell culture -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Bachelor degree in Biology or Chemistry -Work

Line of Business: Aggregates 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 agg plants, Philadelphia portables, Downingtown recycle 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 standa

Required Skills & Experience -Minimum one year of relevant GMP work experience in a lab setting -Bachelor degree in Biology or Chemistry -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) -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols -Proficient with Microsoft Office applications Nice to Have Skills & Experience -1 year of experience working with mammalian cell culture -CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience -Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC -Ability to complete equipment and software qualification protocols -Experience dev

6-month contract to hire 2nd shift Tuesday-Friday (2:30PM - 12:30AM); 10% shift differential Level I- $38/hr, could potentially level up to level II depending on experience The Specialist I is responsible for day-to-day Quality Assurance Operations activities in accordance with cGMPs, CFRs, ICH guidelines and company policies and procedures. The Specialist I will work onsite alongside manufacturing and quality control personnel, helping to ensure that the highest standard of work is performed. This individual is collaborative, organized, innovative, flexible, with a strong desire to learn and take ownership and accountability. The Specialist I will support Quality Assurance lot release and disposition activities including process observation, batch record review, and completion of lot release documentation. The Specialist I supports Quality Assurance initiatives including, but not limited to, review of laboratory investigations and deviation investigations. The successful candidate wil

Our large pharmaceutical client in Malvern, PA is seeking a QC Analyst to join their growing Clinical Release & Stability team to support their Cell Therapy group. The QC Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor. Key Responsibilities: Conduct analytical biological testing of clinical and commercial drug product/drug substance samples Perform peer reviews and approvals of laboratory data Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data Support of New Product Initiatives (NP

Description Is Kymanox the right fit for you? You want to make a difference and have an impact... You enjoy having an influence in your day-to-day work... You are motivated by working alongside a team filled with subject matter experts who will help you learn and grow... You wake up every day and do what you do ... because patients deserve better. If this sounds like you, you've come to the right place. The Manufacturing Quality Specialist will join our Quality Assurance and Compliance team and play a key role in providing quality support for the King of Prussia small-scale device manufacturing facility and process development. The specialist would also support Kymanox's clients with compliance activities, with an emphasis on quality oversight of contract manufacturers and batch production, gap assessments, and phase-appropriate quality management system implementation. Responsibilities: Quality support of daily operations of early-phase or design phase device subassembly manufacturing