QA Lead Technician Pharmaceutical

Bradley Personnel
Lexington, United States of America
1 month ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Senior
Compensation
$ 50K

Job location

Lexington, United States of America

Tech stack

Microsoft Office
Information Technology

Job description

The Quality Assurance Inspector Team Lead plays a critical role in ensuring compliance with cGMP regulations and internal SOPs within a nutraceutical manufacturing and packaging environment. This position is responsible for leading QA inspectors, overseeing inspections, and maintaining the highest standards of product quality, safety, and regulatory compliance., * Support the QA Supervisor in managing daily QA operations

  • Lead and mentor QA Inspectors, ensuring adherence to cGMP and SOPs
  • Monitor manufacturing and packaging processes for compliance and quality
  • Identify and report non-conforming products or practices
  • Conduct pre-production line clearance and approve work areas
  • Inspect in-process and finished goods to ensure quality standards are met
  • Perform routine and random audits of work areas, documentation, and procedures
  • Make quality-based decisions including product acceptance, rejection, or quarantine
  • Assist production staff in identifying defects and non-compliant conditions
  • Enforce cleaning and sanitation procedures per SOPs
  • Review batch records, label control forms, and related documentation
  • Assist in training new employees and ongoing team development
  • Ensure environmental testing and inspections meet NSF requirements

Requirements

Do you have experience in Manufacturing standard operating procedures?, Do you have a High school diploma or GED?, * High School Diploma or GED required

  • Minimum of 2 years of relevant QA or manufacturing experience
  • Strong understanding of cGMP regulations and SOP compliance

Preferred Experience & Skills

  • Knowledge of nutraceutical manufacturing and packaging processes
  • Familiarity with CFR 21 Part 111 and NSF standards
  • Experience identifying product defects and unsanitary conditions
  • Strong documentation review and auditing skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Excellent communication and leadership abilities
  • Proficiency in Microsoft Office and general computer systems

Key Competencies

  • Detail-oriented and highly organized
  • Strong decision-making and problem-solving skills
  • Ability to work independently and as part of a team
  • Effective time management and multitasking abilities
  • Professional communication across departments

Physical Requirements

  • Ability to lift up to 50 lbs occasionally
  • Frequent standing, walking, and use of hands
  • Occasional bending, stooping, kneeling, or crouching
  • Ability to work in a manufacturing environment

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