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 role involves planning, organizing, and leading the effective operation of a production unit, including development projects, resource management, and personnel leadership.
Responsibilities
Plan, organize, and lead the effective operation of the production unit.
Lead and/or participate in development (equipment, processes, products) and efficiency improvement projects.
Ensure effective use of production resources and unit personnel management.
Participate in recruitment, organize employee training, and facilitate optimal use of staff knowledge and experience.
Prepare and submit unit budget plans to management and control expenditure.
Requirements
Augstākā izglītība
Nice to have: Experience leading a team of 50+ employees
Senior Scientist in Inhalations performing complex laboratory testing, method development, validation, and mentorship within a GMP analytical laboratory.
Responsibilities
Independently performs complex laboratory testing
Communicates analytical needs and resources
Maintains strong hands‑on laboratory presence
Assists with testing execution, troubleshooting, and optimization
Applies advanced scientific judgment
Requirements
Bachelor's degree in chemistry, analytical chemistry, pharmaceutical science or related field
As a Senior Chemistry Analyst you will provide technical and scientific expertise within the Quality department, supporting material and product analysis to ensure quality products are supplied to customers on time and in full.
Responsibilities
Review documentation and testing data for components, raw materials, bulk product, CIP samples, water systems, and finished product using the correct procedures in compliance with cGLP, cGMP, Health & Safety, SOPs, environmental and regulatory requirements.
Provide training and support for analysts within the QC department.
Assist with method transfer processes and qualification studies, ensuring timely completion in line with project plans.
Generate, update and implement documentation including SOPs, analytical documents, quality reports, monthly measures and Product Quality Reviews (PQRs).
Contribute to the review, improvement and introduction of laboratory processes to support continuous improvement initiatives.
Requirements
Degree in Chemistry or another relevant scientific discipline
Nice to have: pharmaceutical industry experience
Nice to have: GMP-regulated environment experience
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
Support the Chemistry lab start‑up and perform qualification and routine testing at the Holly Springs Facility, including writing procedures, executing system qualification, method transfers, and managing quality documentation.
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.
Responsibilities
Support the startup of the QC organization by leading QC Chemistry start‑up activities including system qualification and validation and method transfers
Work collaboratively with site teams to establish work order and PM system for laboratory equipment
Assist with review of validation documents to support equipment and computerized system onboarding
Assist with creating and collaborating on Data Integrity Assessments for computerized lab systems
Author, revise and review documents and reports including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports, method assessments, and technical assessments
Requirements
High school/GED
Associate's degree
Bachelor's degree
Master's degree
Nice to have: Degree in Chemistry, Biochemistry, Physics or Chemical Engineering
Support the Chemistry lab start up and perform qualification and routine testing at the Holly Springs Facility, including writing procedures, executing system qualification, method transfers, and managing quality documentation.
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 78,724.45USD -106,509.55 USD
Responsibilities
Support the startup of the QC organization by leading QC Chemistry start up activities including system qualification and validation and method transfers
Work collaboratively with site teams to establish work order and PM system for laboratory equipment
Assist with review of validation documents to support equipment and computerized system onboarding
Assist with creating and collaborating on Data Integrity Assessments for computerized lab systems
Author, revise and review documents and reports including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports, method assessments, and technical assessments
Requirements
High school/GED
Associate’s
Bachelor’s
Master’s
Nice to have: degree in a related scientific field such as Chemistry, Biochemistry, Physics or Chemical Engineering
Support the Chemistry lab start up and perform qualification and routine testing to support the Holly Springs Facility, including writing procedures, executing system qualification, method transfers, and supporting computerized systems.
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
Responsibilities
Participating in the QC Chemistry start up activities including execution of system qualification and validation and method transfers.
Working collaboratively with site teams to establish work order and PM system for laboratory equipment.
Assisting with creating and collaborating on Data Integrity Assessments for computerized lab systems.
Review and Approve QC method executions for GMP and Stability support.
Assisting with procurement activities for consumables and critical reagents for routine lab activities.
Requirements
High school/GED
Associate's degree
Bachelor's degree
Nice to have: degree in a related scientific field such as Chemistry, Biochemistry, Physics or Chemical Engineering
Nice to have: 4+ years of relevant laboratory experience in the GMP commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry
Represent the station Technical Operations department in a professional manner while interacting and coordinating with other departments in the Station Operations Center, Aircraft Routing, Aircraft Dispatch, and Flight Crews.
Responsibilities
Receive and coordinate the recovery of maintenance discrepancies initiated by inbound and outbound flight crews
Coordinate and track the recovery of scheduled deferred items
Notify and communicate the status of aircraft that are out of service or on a maintenance delay to Maintenance Control and Local Operations
Coordinate and track planned maintenance efforts for thru flights
Initiate and update TOC (Technical Operations Computer System) and AMIS logs on all aircraft that are out of service, in a planned hold or have significant maintenance activities on going
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