Senior Chemist
Listed on 2026-10-14
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers
Job Description
We are seeking a highly skilled and self-sufficient High Level Chemist to perform chemical analysis and manage laboratory operations. The ideal candidate will be familiar with FDA requirements, maintain documentation, and ensure compliance with Good Documentation Practices and Standard Operating Procedures. This role offers an opportunity to grow within a small team and eventually lead your own team.
Responsibilities- Perform analysis of chemicals and finished products.
- Maintain and record all data using Good Documentation Practices.
- Order and maintain adequate supplies needed for testing.
- Conduct peer reviews of other analysts' work for accuracy.
- Perform laboratory maintenance duties as needed.
- Author and edit applicable Standard Operating Procedures and test methods.
- Ensure compliance with Good Laboratory Practice (GLP) requirements.
- Maintain and calibrate lab instrumentation per Company SOPs.
- Monitor unit performance and take proactive measures to ensure proficiency, efficiency, and conformance to cGMP.
- Review and approve specific quality documentation including raw materials, finished products, consumer complaints, lab incidents and investigations, and annual product reports.
- Initiate and conduct continuous improvement initiatives for the laboratory.
- Practice safe laboratory operations.
- Direct interface with laboratory equipment service providers.
- Cross-train in the microbiological laboratory.
- Proficiency with HPLC and GC equipment.
- Expertise in all common laboratory techniques, including reagent preparation and labeling.
- Ability to perform basic mathematical and scientific calculations.
- Experience with analytical chemistry, wet chemistry, and titration.
- Knowledge of FDA requirements for laboratory personnel.
- Strong organizational and detail-oriented skills.
- Ability to work independently and accomplish tasks.
Skills & Qualifications
- Experience with gas chromatography (GCMS).
- Knowledge of raw material testing.
- Familiarity with quality control and analytical development.
- Experience in a pharmaceutical setting.
This position is based in a pharmaceutical company with a smaller team of about 10 employees. The role requires working in a laboratory setting, maintaining and calibrating lab instrumentation, and ensuring compliance with safety and regulatory standards. Work hours are Monday to Friday, from 7 AM to 3:30 PM.
Job Type & LocationThis is a Contract to Hire position based out of Rockledge, FL.
Pay and BenefitsThe pay range for this position is $33.00 - $40.00/hr.
Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
This is a fully onsite position in Rockledge, FL.
Final date to receive applicationsThis position is anticipated to close on Mar 25, 2025.
Equal Opportunity Employer The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccom for other accommodation options.
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