Entry-Level Pharmaceutical Packaging & Inspection Tech

STAQ Pharma; Denver (CO); On-site; USD 28,000 - 39,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability coverage

401(k) with employer match

Paid time off

7 paid holidays

Professional growth

Job summary

STAQ Pharma is seeking a Production Technician I to join our 503B outsourcing facility in Denver. This entry-level role supports finished product inspection, labeling, packaging, documentation, cleaning, and material handling, ensuring adherence to cGMP and regulatory requirements.

Work is performed in a controlled non-classified manufacturing environment with proper PPE, detailed procedures, and a strong emphasis on accuracy, safety, and collaboration across shifts to maintain product quality

Qualifications

• High School Diploma or equivalent required.
• Must pass drug and vision screening.
• Must speak, write, and read English.
• 1+ year of continuous work experience in a regulated environment preferred.
• Knowledge of basic arithmetic and chemistry calculations is a plus.

Responsibilities

• Perform visual inspection of finished products and verify labels and packaging.
• Support labeling, packaging, cleaning, restocking, and documentation tasks.
• Follow batch records, SOPs, and cGMP practices accurately.
• Complete production documentation in real time with legible entries.
• Handle chemicals and materials per safety procedures and PPE requirements.
• Identify deviations and escalate safety or quality concerns promptly.
• Maintain training and qualifications for production activities.

Skills

Learning agility

Accuracy under pressure

Team collaboration

Attention to detail

Safety compliance

Punctuality and reliability

Adaptability to shifting priorities

Education

High School Diploma

Job description

STAQ Pharma is seeking a Production Technician I to join our 503B outsourcing facility in Denver. This entry-level role supports finished product inspection, labeling, packaging, documentation, cleaning, and material handling, ensuring adherence to cGMP and regulatory requirements.

Work is performed in a controlled non-classified manufacturing environment with proper PPE, detailed procedures, and a strong emphasis on accuracy, safety, and collaboration across shifts to maintain product quality