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
$ 50KJob 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