Job Title: Production Associate
Job Type: Temporary to Hire
Location: Alpharetta, GA (Fully On-Site)
Shift: Monday – Friday, 7:00am - 3:30pm
Pay Rate: $17.00/hour
Position Summary
We are seeking a reliable and detail-oriented Production Associate to join our manufacturing team in Alpharetta. This position is responsible for supporting the production of medical device components through assembly, inspection, packaging, and labeling while ensuring compliance with company quality standards and regulatory requirements. The ideal candidate thrives in a fast-paced, quality-focused environment and demonstrates strong attention to detail.
Essential Job Duties & Responsibilities
- Follow detailed work instructions to manufacture, assemble, inspect, package, seal, sterilize, and box RMI and CM products and their components.
- Ensure all products are assembled and packaged according to company specifications and quality standards.
- Review work orders to verify correct product labels and ensure labels are properly applied to products and packaging according to instructions.
- Store completed products in the designated “wait for release” area and move them to the “released” area once Quality Assurance has approved them.
- Maintain accurate production and documentation records in accordance with Good Documentation Practices (GDP).
- Adhere to hygiene, gowning, and cleanliness requirements specific to the assigned work area.
- Comply with all company procedures, work instructions, drawings, specifications, and Quality System requirements.
- Follow all applicable GMP, GDP, ISO, and FDA regulations related to medical device manufacturing.
- Perform routine inspections to ensure products meet quality standards and report any discrepancies to supervisors.
- Maintain a clean, organized, and safe work environment.
- Support team members and supervisors with additional production tasks as needed.
Qualifications & Requirements
- High School Diploma or GED preferred.
- Previous manufacturing, production, or assembly experience preferred.
- Experience working in a medical device, pharmaceutical, or FDA-regulated environment is a plus.
- Ability to read, understand, and follow written and verbal instructions in English.
- Strong attention to detail and ability to work in a fast-paced, quality-driven environment.
- Good hand-eye coordination and manual dexterity for handling small components.
- Ability to follow GMP, GDP, ISO, and FDA regulatory requirements.
- Ability to stand for extended periods and perform repetitive tasks as required in a production setting.
- Strong reliability, teamwork skills, and commitment to maintaining quality and safety standards.
TRC Talent Solutions is proud to be an Equal Opportunity Employer (EOE). All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, protected veteran status, disability status, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by law. At TRC, we take pride in fulfilling our opportunity to add value to our client's business as their staffing partner, while working tirelessly to connect thousands of individuals each year with work opportunities where they can meet the needs of their families and have the potential to build their careers.