As a QC Technician, you will timely sample and inspect materials under cGMP and as per the Quality Department SOPs and Specifications, a variety of materials including API (Active Pharmaceutical Ingredients), raw materials, intermediates and finished products.
Compensation
Hourly range: $24.04 - $44.38.
Responsibilities
Samples all raw materials in accordance with cGMP regulations and Sampling Manual SOP.
Samples and inspects raw material packaging in accordance with cGMP regulations and Sampling Manual SOP and Specifications.
Samples packaging material and delivers to the raw material laboratory in accordance with Sampling Manual SOP.
Tracks & places all raw material and finished product retains in storage within either room temperature, cold room, or freezer environments.
Send out samples via FedEx desk to outside laboratories for Quality Department requests.
Requirements
Bachelor’s degree in a relevant Scientific discipline (chemistry preferred)
Nice to have: GMP quality control
Nice to have: pharmaceutical manufacturing
Nice to have: Nutritional Supplements manufacturing facility
The Manufacturing Manager I leads and drives the execution of manufacturing processes for cell therapies under cGMP, overseeing a team focused on safety, compliance, and continuous improvement.
Compensation
Bothell - WA - US: $113,930 - $138,051
Responsibilities
Manages creation, implementation and compliance of all Source Governing Documents
Oversees operations within a validated manufacturing system
Plans, assigns resources and oversees daily operational activities
Maintains operating and storage areas for compliance and safety
Drives right-first-time initiatives and holds team accountable for compliance
Requirements
Bachelor's in relevant science or engineering discipline or equivalent
Entry-level microbiologist role focused on environmental monitoring, microbial enumeration, identification, and testing of raw materials and utilities within a cGMP environment.
Responsibilities
Perform all microbiological testing of raw materials, utilities, and in-process, and final products/stability testing.
Perform daily, weekly, semi-weekly, and monthly environmental monitoring of the manufacturing environment.
Perform enumeration and organism identification including culturing, isolating, entry, and maintaining of organisms.
Document and review raw and final data to ensure complete and proper documentation according to procedures and applicable cGMPs.
Notify Microbiology Laboratory management immediately of out of specification (OOS) results.
Deliver the IFB CAPEX Project Safely, on Time, & on Budget for a highly regulated campus, leading all engineering-related activities and ensuring alignment between IFB and InsuLINK programs.
Responsibilities
Lead the IFB Engineering activities during the execution phase of the project
Identify and onboard the appropriate Engineering staffing for the project execution
Define together with Purchasing the best contract model for all key steps from Detail Engineering, Construction & C&Q activities
Collaborate with IFF Program teams during execution phase, developing optimized solutions leveraging Frankfurt process replication while integrating China local rules & codes
Build an aligned strategy with Program Design team, purchasing & Engineering contractor to secure construction down to mechanical completion
Requirements
Masters degree in Project Management, Mechanical or Process Engineering
Lead and monitor inspection process activities on the manufacturing floor, ensuring compliance with SOPs, cGMPs, and continuous improvement initiatives.
Compensation
Our target base pay hiring range for this position is $26.00 - $40.50 per hour.
Responsibilities
Lead and monitor inspection process activities to ensure successful operations on the production floor
Perform inspection activities as needed to support floor coverage and qualification maintenance
Perform inventory control and reconciliation activities using SAP and WES
Execute protocols as required as part of equipment qualification and process validation work
Ensure work requirements are followed on the production floor in accordance with SOPs and cGMPs
Requirements
High school graduate, vocational school graduate, or equivalent
Lead quality assurance and compliance for veterinary medicine research and development, ensuring regulatory and GMP standards across product development, manufacturing, and supplier processes.
Responsibilities
Ensure compliance with USDA, EU, FDA, and Zoetis quality standards
Collaborate with DST on scale‑up and technical transfers
Serve as QA consultant for development, clinical, and VICH batches
Review and approve master batch records, validation protocols, and deviation investigations
Approve changes to manufacturing and packaging processes and IT systems
Requirements
Bachelor's degree in biological or pharmaceutical sciences, engineering, or related discipline
Nice to have: Master's or PhD in biological science or chemical/bioprocess engineering
Nice to have: expert-level competency in validation of processes, equipment, cleaning procedures, software, and computerized systems
Nice to have: solid knowledge of Zoetis biological and biopharmaceutical products
Third shift manufacturing operator role in a cleanroom environment, performing specialized tasks, following SOPs and GMP requirements, and participating in a Lean PPI culture.
Responsibilities
Perform specialized tasks within the production environment including line lead responsibilities
Read intricate manufacturing drawings and follow standard operating procedures
Manufacture chambers utilizing Standard Operating Procedures (SOP) in accordance with product blueprint
Record and complete accurate documentation according to GMP requirements
Operations Specialist supporting shop floor execution, batch closeout, and troubleshooting in a GMP manufacturing environment.
Compensation
The salary range for the primary location of this role is: $79,200.00 - $124,700.00. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable.
Responsibilities
Partnering with the Operations management team to create and execute strategies that support design, development, delivery and evaluation of projects related to steady‑state production and/or continual process improvement.
Authoring and reviewing documents and SOPs.
Batch Record Review.
eLog Review.
Lead safety investigations.
Requirements
High School Diploma
Bachelor’s degree in a technical field
Bachelor's degree in a direct GMP, biotechnology, manufacturing setting
Nice to have: Understanding of MPS methodologies
Nice to have: Experience with shop‑floor cGMP manufacturing and related systems (i.e. SAP)
Senior Quality Assurance Associate responsible for quality assurance in Pfizer’s Quality Risk Management program at the McPherson site.
Compensation
The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.
Responsibilities
Responsible for SME strategic review and evaluation of quality risk assessments and potential risks that impact the McPherson plant
Monitors quality system metrics and executes actions to ensure quality system performance
Provide support and act as liaison to business units, corporate, and stakeholders for quality risk management process
Serve as the McPherson site resource for quality risk management
Acts as quality authority for quality risk management
Manager, ManufacturingNewBristol Myers Squibb · Bothell, US