Quality Control Chemist I

Job Overview

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Compensation

Salary
Range $70,500.00 - $72,000.00
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Work Schedule

Standard Hours
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Benefits

Health Insurance
Dental Insurance
Paid Time Off
Retirement Plan
Professional Development
Employee wellness programs
Flexible spending account

Job Description

CAPTEK Softgel International is a distinguished global leader in the development and production of high-quality nutraceutical supplements. As a Contract Manufacturer Organization (CMO), CAPTEK collaborates closely with innovators from some of the world's most successful brands, ensuring the delivery of superior dietary supplement products. With an extensive reputation for excellence in manufacturing and quality assurance, CAPTEK is committed to championing wellness worldwide by providing trusted softgel supplements that meet stringent standards of purity, potency, and safety.

The position of Quality Control Chemist at CAPTEK Softgel International plays a crucial role in maintaining these high standards. This role involves testing and contracting necessary tests to third-party laboratories for all ingredients involved in softgel production to verify identity, purity, strength, and composition. The Quality Control Chemist ensures that the content of finished softgel product capsules complies with all established specifications, guaranteeing that each product released meets the highest quality expectations before reaching customers. This role requires a sophisticated understanding of analytical chemistry techniques and the ability to operate a variety of scientific instruments including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectrophotometry, Atomic Absorption Spectrometry, and Fourier Transform Infrared (FTIR) spectroscopy.

The chemist's responsibilities extend to generating accurate Certificates of Analysis (CoA) for raw materials and finished products, creating and modifying Standard Operating Procedures (SOPs) and test methods, as well as collaborating with laboratory teams, microbiologists, and technicians to ensure smooth operational flow and compliance with safety and cGMP (current Good Manufacturing Practice) regulations. The role demands a high level of meticulousness in documenting procedures, safe handling of hazardous materials, and adherence to CAPTEK's policies and federal safety standards such as HACCP and Safety Defense.

CAPTEK values professionals who demonstrate excellent analytical skills, problem-solving abilities, and a collaborative approach to work. The Quality Control Chemist is expected to handle multiple projects simultaneously, adapt to evolving business pressures, and maintain professionalism in all communications. This role also requires the ability to work with advanced scientific concepts involving statistical theory and complex instrumentation software, alongside proficiency in computer applications such as Microsoft Word, Excel, SysPro, and UniPoint.

Working at CAPTEK means being part of an environment that prioritizes employee safety, quality management, and ongoing professional development. The work environment involves occasional exposure to toxic or caustic chemicals, and employees must observe strict safety protocols to mitigate risks including chemical burns, electrical hazards, and fire. The physical demands include extended periods of sitting, walking, lifting of objects up to 50 pounds, and performing tasks that require fine motor skills and close vision.

Joining CAPTEK Softgel International as a Quality Control Chemist is an opportunity to contribute to a global leader focused on enhancing health and wellness through nutraceutical innovation. This full-time role is ideal for individuals with a bachelor’s degree or higher in chemistry, several years of laboratory experience, and a commitment to quality assurance excellence. By becoming part of the CAPTEK team, you can expect to be engaged in meaningful scientific work that directly impacts consumer health worldwide while advancing your career in a progressive and supportive manufacturing environment.

Job Requirements

  • Minimum bachelor's degree in chemistry or related field
  • Two to ten years of relevant laboratory experience or equivalent combination
  • Ability to operate analytical instrumentation such as HPLC, GC, UV-Vis, FTIR
  • Knowledge of cGMP, HACCP, and safety procedures
  • Strong communication and teamwork skills
  • Capacity to handle multiple projects and meet deadlines
  • Physical ability to perform laboratory work including lifting up to 50 pounds
  • Willingness to adhere to all safety protocols
  • Proficient with laboratory software and computer applications
  • Good judgment and analytical thinking
  • Ability to handle hazardous chemicals safely
  • Flexible and dependable work ethic
  • Strong organizational and documentation skills

Job Qualifications

  • Bachelor's degree in chemistry or related field
  • Two to ten years related laboratory experience
  • Strong analytical and problem-solving skills
  • Proficiency with HPLC, GC, UV-Vis, FTIR instrumentation software
  • Familiarity with cGMP, HACCP, and quality management practices
  • Excellent oral and written communication skills
  • Ability to work collaboratively in a team environment
  • Knowledge of scientific and technical journals and test methods
  • Ability to interpret and apply advanced scientific and mathematical concepts
  • Competence in Microsoft Word, Excel, SysPro, and UniPoint
  • Strong attention to detail and adherence to safety protocols
  • Ability to adapt to changes and handle multiple priorities
  • Commitment to ethical practices and professional conduct

Job Duties

  • Use HPLC, GC, UV-Vis spectrophotometer, and other analytical instruments to test dietary supplement raw materials and finished products
  • Notify supervisor promptly of out-of-specification test results and participate in investigations
  • Ensure accuracy and compliance of Certificates of Analysis before material release
  • Generate and verify finished product Certificates of Analysis claims
  • Develop and revise SOPs and test methods and ensure adherence by QC staff
  • Perform FTIR spectroscopy to confirm identities of raw materials and products
  • Prepare samples, solvents, calculate data, document procedures, and safely dispose of hazardous chemicals
  • Safely operate laboratory tools and appropriately handle chemical reagents
  • Accurately weigh, label, log, and document all samples and materials
  • Collaborate with technicians and scientists to ensure proper communication and workflow
  • Adhere to safety, cGMP, HACCP, and Captek Standard Operating Procedures
  • Manage multiple projects and work effectively under pressure
  • Participate in maintaining laboratory safety and quality standards

Job Criteria

Experience

Mid Level (3-7 years)


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