Experienced Validation Engineer to support equipment qualification and cleaning validation at a biopharmaceutical manufacturing facility.
Compensation
Pay Rate: $65-$83/hr (paid weekly)
Responsibilities
Author, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for manufacturing equipment and systems.
Develop and execute Cleaning Validation (CV) and cleaning verification protocols, including sampling plans, visual inspections, and coordination of analytical testing.
Support qualification and validation activities for GMP manufacturing equipment, including bioreactors, chromatography skids, tangential flow filtration (TFF) systems, and autoclaves.
Sr. Scientist – Quality Control, responsible for performing in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs in a GMP laboratory setting.
Compensation
The salary range estimated for this position based in Massachusetts is $95,000.00–$100,100.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Responsibilities
Perform in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs
Maintain accurate testing records and adhere to cGMP/GDP expectations
May participate in executing method validations and/or method transfers
Assist in troubleshooting of analytical methods with the assistance of manager when necessary
May participates in author and review of data, SOPs, analytical methods, protocols and reports
Requirements
Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
Author, review, and execute equipment qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
Develop and execute Cleaning Validation (CV) and cleaning verification protocols for manufacturing equipment and systems
Develop cleaning validation sampling plans, conduct visual inspections, and coordinate analytical testing, including TOC, conductivity, bioburden, and endotoxin
Perform equipment qualification and validation activities for bioreactors, chromatography skids, TFF systems, autoclaves, stainless steel equipment, and single-use manufacturing systems
Support Clean-in-Place (CIP) and Steam-in-Place (SIP) validation activities
Requirements
Bachelor's or Master's degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Biochemistry, or a related technical discipline
Support the QC analytical chemistry team by performing testing HPLC/UHPLC, CE, CEX, HILIC and related assays, managing samples and data, maintaining equipment, and contributing to method development and compliance.
Compensation
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 62,571.90USD -84,656.10 USD
The Industrial Engineer Intern joins the Operational Excellence team to analyze and improve manufacturing line performance using Discrete Event Analysis and Lean methodologies.
Locations (4)
Tempe, Arizona, United States
San Jose, California, United States
San Francisco Bay area, California, United States
New York City, New York, United States
Compensation
$20.91 - $56.97 / hourly. For specific work locations within San Jose, the San Francisco Bay area and New York City metropolitan area, the base pay range for this role is $25.96 - $67.07/ hourly
The Chemistry Intern will gain hands-on experience in applied chemistry and analytical testing and support the Reprocessing Product Development team supporting new product development and sustaining of existing products, including cleaning, disinfection, and sterilization chemistries.
Compensation
Pay range for this opportunity is $20-25/hr.
Responsibilities
Assists in formulating, preparing, and documenting chemical solutions and prototype formulations to meet company, team and group goals.
Performs analytical testing and characterization of chemistries and raw materials using laboratory instrumentation (e.g., HPLC, GC, UV-Vis, pH, titration).
Writes test protocols and reports, and maintains laboratory notebooks in accordance with Good Documentation Practices.
Collects and analyzes data.
Supports stability, material compatibility, and cleaning efficacy studies.
Requirements
Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering or related
Coordinate and manage maintenance activities for United Airlines aircraft at the San Francisco hub, ensuring compliance with FAA regulations and operational performance goals.
Compensation
The base pay range for this role is $131,456.70 to $160,669.30. The base salary range/hourly rate listed is dependent on job-related, factors such as experience, education, and skills. This position is also eligible for bonus and/or long-term incentive compensation awards.
Responsibilities
Coordinate recovery of maintenance discrepancies from flight crews
Track scheduled deferred items
Notify Maintenance Control and Local Operations of aircraft status
Responsible for performing laboratory testing of raw materials, drug substances, drug products, in-process samples, and stability samples using analytical instrumentation.
Compensation
Pay: $40.00- 44.00/hr to start.
Responsibilities
Perform laboratory testing of raw materials, drug substances, drug products, in-process samples, and stability samples using analytical instrumentation
Conduct routine wet chemistry and analytical testing using HPLC, GC, UV-Visible Spectroscopy, CGE, ICE, polarimeters, osmometers, pH meters, conductivity meters, and TOC analyzers
Industrial Engineer InternViasat, Inc. · Tempe, US+3 more
Chemistry Intern - Summer 2027STERIS Corporation · Plymouth, US
Hub Maintenance CoordinatorUnited Airlines · San Francisco, US