Production Associate I - 2nd Shift (B1)

Beauty Manufacturing Solutions Corp•Coppell, TX

6d•Onsite

About The Position

Production Associate I is responsible for performing assembly, filling, labeling, inspection, and packaging of finished goods in compliance with current Good Manufacturing Practices (cGMP), FDA regulations, company procedures, and safety standards. This role supports daily production operations while ensuring quality, productivity, safety, and compliance requirements are consistently met.

Requirements

Ability to read, understand, and follow work instructions, SOPs, and production documentation.
Basic understanding of GMP and workplace safety requirements.
Ability to identify basic product defects and packaging inconsistencies.
Basic math skills, including counting, verifying quantities, and completing production records.
Ability to perform assigned production operations in accordance with approved work instructions.
Ability to complete required production and quality records accurately.
Ability to work cooperatively with Line Leads, Supervisors, and other team members.
Ability to complete required training and demonstrate proficiency in assigned operations.
High school diploma or GED required.
Ability to stand and walk for extended periods during the work shift.
Frequent bending, squatting, kneeling, reaching, twisting, and climbing.
Ability to lift, carry, push, and pull up to 50 pounds, with or without reasonable accommodation.
Exposure to typical manufacturing environments including noise, moving equipment, airborne particles, cleaning agents, and temperature variations.
Ability to distinguish colors, shades, and visual product characteristics for quality inspection.
Must be able to read labels that could contain small fonts.
Frequent performance of repetitive motions involving hands, wrists, fingers, and arms.
Required to wear personal protective equipment (PPE), including safety glasses, gloves, hairnets, beard covers, and safety footwear.

Nice To Haves

0–2 years of manufacturing experience preferred.
Experience in cosmetics, OTC, pharmaceutical, food, or dietary supplement industries is a plus.
GMP manufacturing experience preferred.

Responsibilities

Maintain a clean, organized, and safe work environment in compliance with GMP, company policies, and established procedures including Lockout/Tagout (LOTO) and emergency stop (E-Stop) requirements.
Follow all company safety rules, policies, and report unsafe conditions or behaviors immediately.
Perform assembly, filling, bottling, capping, labeling, inspection, sorting, and packaging operations according to production schedules and work instructions.
Conduct visual inspections of finished goods, labels, lot codes, and packaging components to ensure compliance with quality requirements.
Stop work immediately, notify the Line Lead or Supervisor or Manager, and support initiation of a Notification of Event (NOE) in ETQ for any deviation from the process instruction, product defects, equipment issues, safety hazards, and quality deviations.
Support line clearance activities and maintain proper housekeeping before, during, and after production runs.
Handle raw materials, components, and finished goods according to established procedures.
Maintain regular and reliable attendance and punctuality in accordance with the Employee Attendance Punctuality Policy.
Be available to work overtime and occasional weekend shifts as production needs require.
Observe personal hygiene and gowning requirements, and report to a supervisor any apparent illness, open lesion, or other health condition that may adversely affect product safety or quality, as required by 21 CFR 211.28.
Follow and abide by the Company Employee Handbook at all times.
Perform other related duties or projects as required.