The Analytical Quality Assurance (AQA) associate I position is a team contributor role responsible for reviewing and confirming compliance related to raw materials, in-process and finished product analytical documents.
Compensation
$66,300 - $86,000
Responsibilities
Reviewing and confirming the compliance related to raw materials, in-process and finished product analytical documents
Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel during routine operation
Verifying the laboratory chemicals/reagents, standards for completeness of the labels against standard operating procedures (SOPs)
Review of laboratory audit trials during data review against standard operating procedures (SOPs)
Coordinating with the Analytical Laboratory Teams to arrange required documents to cross functional teams
Requirements
Bachelor's degree in chemistry, Pharmaceutical Sciences, or related field of study
Master’s degree in chemistry, Pharmaceutical Sciences, or related fields of study (preferred)
Nice to have: Master’s degree in chemistry or Pharmaceutical Sciences
Nice to have: Experience in Inhalation products (MDI)
Nice to have: Knowledge of good manufacturing practices and good documentation practices
Perform laboratory analysis and sampling of raw materials, intermediates, finished products, cleaning verification samples, stability samples and other miscellaneous samples following relevant SOP’s while adhering to current Good Manufacturing Practices (cGMP) to ensure they meet the required quality standards and specifications.
Compensation
The salary range for this role is $60,000–$70,000.
Responsibilities
Perform laboratory analysis and sampling of raw materials, intermediates, finished products, cleaning verification samples, stability samples and other miscellaneous samples following relevant SOP’s while adhering to current Good Manufacturing Practices (cGMP) to ensure they meet the required quality standards and specifications.
Perform basic maintenance of technical equipment, use of basic troubleshooting techniques and laboratory stock management
Deliver experimental output with a high degree of scientific integrity, both on time and on target, with a focus on quality.
Actively demonstrate strict compliance with current Good Manufacturing Practices and Good Documentation Practices (cGMP and GDP), Environment, Health and Safety (EH&S) and other relevant standards in all aspects of work.
Manages data by following established procedures, standards and processes. Uses the concepts of ALCOA+ to maintain Data Integrity.
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
Conducts chemical, physical, and microbiological analysis of raw materials and yeast products in a laboratory setting, ensuring accurate testing and compliance with safety protocols.
Locations (2)
Cedar Rapids, Iowa, United States
Dothan, Alabama, United States
Responsibilities
Conducts microbiological analysis of samples and preparation of pure culture yeast for use in fermentations
Conducts chemical and physical analysis of raw materials and yeast, both in-process and finished product
Performs tests such as nitrogen, phosphorus, pH, color, percentage of Buds, dry matters, sugar, brix, and yeast activity using Risograph
Maintains laboratory equipment and work area, including cleaning, calibration, and record-keeping
Prepares chemical solutions for processing areas and ensures supply of needed solutions
Requirements
Associate Degree in Microbiology, Chemistry, Food Science or related field
Compounding Supervisor - 2nd Shift
Beauty Manufacturing Solutions Corp · Posted Nov 10, 2026
Oversee the Compounding department to ensure timely, high‑quality production of personal care products while maintaining safety, cleanliness, and compliance.
Responsibilities
Manage Compounding Department staff
Interview, train, supervise, counsel, discipline, and evaluate personnel
Report safety violations to Compounding Manager/Director of Operations and Safety Committee
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