QA Lead, Quality Assurance - QA​/QC, Quality Technician​/ Inspector

Posted Thursday, February 5, 2026 at 11:00 AM

Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands.

Summary: It is the responsibility of the QA Lead to assist and support the QA Supervisor in the oversight of QA activities and training of new hires.

• The QA Lead is responsible for the supervision of QA Technicians.
• Assist QA management in providing direction, assigning tasks, and training.
• Assist in training new inspectors on proper documentation and inspection techniques.
• Assist in training of plant personnel in GMPs.
• Monitor HACCP and Food Safety adherence.
• Assist management in creating quality plans and procedures.
• Assist with quality decisions with respect to product non-conformances.
• Recommend corrective actions for quality issues.
• Assist in preparation for customer and regulatory inspections.
• Perform and document a wide variety of inspections, checks, tests, and/or sampling procedures.
• Monitor all aspects of the manufacturing operations and report non-conformances to the supervisor.
• Assist management in conducting inquiries and investigations.
• Review documentation to assure accuracy and completeness, and to prevent errors.
• Perform reconciliation and closing of batch records both in hard copy and electronic systems.
• Ensure timely release of finished goods.
• Disposition of products in the absence of Supervisor.
• Perform other related duties as assigned by management.

• Minimum of 4 years of relevant work experience with 2 years in a Lead role.
• Good verbal and written communication
• Good interpersonal skills
• Ability to work independently and in a team environment
• Ability to follow instructions
• Good attendance and punctuality
• Excellent Organization skills/ attention to detail/ ability to work effectively in a fast-paced environment

• Education:
  
  Minimum High School Diploma or equivalent.
• Working knowledge of cGMPs and FDA regulations
• General proficiency in using Microsoft Word, Excel, Outlook, and Power Point

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts; fumes, or airborne particles and risk of electrical shock.

The noise level in the work environment is usually moderate.

CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants.

We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law.

Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment.

Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.