Quality Specialist I
Quick Summary
About Company At the heart of what we are, we are a small company that specializes in manufacturing personal care products.
At the heart of what we are, we are a small company that specializes in manufacturing personal care products. While we are much bigger now than what we were 20 years ago or even 5 years ago, our company was built on a belief that being small meant that we had to be faster than our competition, smarter, braver and of course, nicer. We knew that in order to make it, we had to produce products that our customers needed, in time, priced right, and with the highest quality. We knew innovation meant pushing the envelope on design and thinking. Most importantly, we knew that developing relationships meant building a reputation for coming through on promises and standing behind our product. That is who we are today and how we operate every day.
- The Quality Specialist is responsible for ensuring that personal care products meet established quality standards and comply with regulatory requirements. This role involves conducting quality sampling, inspections, audits, and various product testing, including but not limited to microbiological, analytical, organoleptic, and physical tests. Additionally, the Quality Specialist is responsible for developing and implementing quality assurance processes to ensure product safety, efficacy, and consistency.
Responsibilities
~1 min read- →Conduct quality inspections of raw materials, in-process products, and finished goods.
- →Perform routine and non-routine tests to ensure product compliance with specifications and
- →standards.
- →Monitor and analyze quality control data and test results.
- →Ensure products comply with local, national, and international regulations (e.g., FDA, ISO).
- →Prepare and maintain documentation required for regulatory compliance and audits
- →Maintain detailed and accurate records of all testing results, comments, deviations, and control
- →information.
- →Perform root cause analysis and suggest appropriate corrective actions (OOS Investigations).
- →Maintain proper labeling, handling, storage, use, and disposal of solutions, biohazard and
- →hazardous waste, and microbiological cultures.
- →Calibrate and maintain lab equipment to ensure accuracy and reliability
- →Maintain laboratory inventory of items and PO requests in coordination with the QA/QC Manager.
- →Support the QA/QC Manager as necessary during environmental monitoring projects.
- →Strong team player with personal commitment towards business’ goals and customers’ goals.
- →Perform additional duties as assigned.
- Proficiency in serial dilutions, aseptic testing, growth promotion, microbial monitoring, gram
- staining, plating, membrane filtration required.
- Proficiency with HPLC and ICP-MS preferred.
- Experience with Microsoft Office Suite (Excel, Word, Outlook).
- Thorough knowledge of classical microbial culture methods (FDA-BAM, APHA, USP).
- Critical thinking and problem-solving skills are essential for this position.
- High attention to detail.
- Thorough knowledge of USP 61 and USP 62 validation and suitability studies.
- Great communication skills (oral and written).
- A basic knowledge of laboratory safety procedures and practices is required to ensure a safe working environment.
- 1 year relevant industry experience preferred. • A Bachelor's degree (4-year degree) in Microbiology, Chemistry, Food Science, or a related discipline is required.
- Alternatively, 2 years of relevant experience may be considered in place of the degree requirement.
Requirements
~1 min read- Must be able to climb stairs, stand for long periods of time, lift up to 40 pounds and have the ability to bend.
Location & Eligibility
Listing Details
- First seen
- August 26, 2026
- Last seen
- August 26, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 52%
- Scored at
- August 26, 2026
Signal breakdown
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