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
The role involves independently performing complex laboratory testing and providing hands-on technical coaching and mentorship within the laboratory, specifically focusing on Mass Spec/Extractable and Leachables.
Responsibilities
Independently performs complex laboratory testing, including challenging routine testing, analytical investigation support, development, transfer, or validation activities.
Communicates analytical needs, resources, and/or barriers with relevant stakeholders.
Maintains a strong hands-on laboratory presence and serves as a technical resource during test execution.
Actively assists with testing execution, troubleshooting, and optimization rather than directing work from outside the lab.
Applies advanced scientific judgment to execution strategy, data interpretation, and problem resolution.
Requirements
Bachelor's degree in a relevant area, ie. chemistry, biochemistry
A senior scientific contributor providing technical leadership for complex analytical activities, method development, and validation within biopharmaceutical programs.
Responsibilities
Provide technical leadership and oversight for complex, non-routine analytical testing, including method development, validation, transfer and method establishment activities.
Serve as a subject matter expert for one or more analytical technologies, platforms, assays or scientific disciplines.
Design, execute and oversee complex laboratory experiments and analytical activities.
Guide scientific decision-making around experimental design, execution strategy, data interpretation and troubleshooting.
Maintain an active laboratory presence, providing hands-on scientific support and ensuring alignment between technical strategy and laboratory execution.
Requirements
Bachelor’s degree or equivalent relevant academic/vocational qualification
The Staff Scientist provides expert-level technical leadership within the laboratory as a senior scientific contributor and recognized technical authority. This role delivers oversight for nonroutine programs (analytical development, validation, transfer) and/or serves as a subject matter expert (SME) for specific analytical technologies, while maintaining an active laboratory presence.
Responsibilities
Provides technical oversight for complex, non-routine analytical testing (analytical development, validation, and transfer), method establishment, and technology-driven programs.
Serves as a senior technical authority and SME for one or more analytical technologies, platforms, or scientific disciplines.
Guides scientific decision-making to ensure appropriate experimental design, execution strategy, and data interpretation.
Reviews and/or approves technical documents including methods, protocols, reports, and quality records to ensure quality and compliance.
Support pharmaceutical development in a GxP-regulated laboratory performing analytical testing, method development, and validation.
Compensation
Compensation: $85,000-$95,000 per year
Responsibilities
Perform complex analytical testing using techniques such as HPLC, UPLC, LC-MS, GC, GC-MS, UV/Vis, FTIR, spectroscopy, dissolution, and supplementary wet chemistry in accordance with SOPs and GxP requirements.
Lead analytical method development, optimization, and validation activities to ensure methods are suitable for intended use and compliant with regulatory requirements.
Analyze and interpret data, troubleshoot analytical issues, and prepare clear summaries, technical reports, and documentation of experimental results.
Document procedures, observations, results, deviations, and investigations accurately in laboratory notebooks, LIMS, and other required systems.
Lead and facilitate OOS and OOT investigations, help identify root causes, and support corrective and preventive actions.
Requirements
Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field
Analysis of in process, intermediate, raw material, packaging material, ETP and utility samples, stability samples, R&D samples and other samples as per plant requirement as per defined STP’s.
Calibration of all equipment in QC department as per SOP’s.
Maintain the records of calibration, working standards, stability data, AMC, outside calibration records, instrument log book, validation report, in process and intermediates test reports as per GLP.
Perform analytical method validation as and when required.
Perform analytical method development project as and when required.
Lab/Facility Chemist performs chemical analyses of hazardous and non-hazardous waste to determine compliant treatment and disposal.
Compensation
The pay range for this position is $22.85 to $31.40* which reflects the minimum wage in multiple jurisdictions. The actual range will depend on the locality in which you are hired.
Responsibilities
Performs preparation techniques and instrumental analysis of environmental samples
Participates in the generation of SOPs and Work Instructions
Prepares samples for laboratory equipment
Utilizes instrument sequencing and data processing
Validates methods for testing organics and inorganics
Requirements
No degree required but 3 years relevant work experience
Supports the Quality Management System (QMS) and Document Management System (DMS) in a GMP regulated environment, ensuring compliance with SOPs, GMP/GLP standards and client requirements.
Compensation
The hiring range in Colorado for this position is $93,750/year - $108,750/year and is eligible for a 4% annual target bonus.
Responsibilities
Perform independent quality evaluation and release of support documentation, materials, products, equipment, and/or facilities
Ensure testing/manufacturing performed per approved SOPs/methods/protocols and comply with specifications
Participate in internal, client and/or regulatory audits
Support quality events and root cause analysis
Develop, implement, and maintain procedures and policies to comply with FDA, EU, and ICH requirements
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