Manufacturing Associate

Tailstorm-Health-Inc; Chandler (AZ); On-site; USD 41,000 - 50,000; Full time

Job summary

Tailstorm-Health-Inc is hiring a Manufacturing Associate in Chandler, AZ to support pharmaceutical manufacturing under cGMP and safety standards. The role involves sterile processes, strict documentation, and collaboration with Quality, Engineering and Maintenance teams.

The ideal candidate has a high school diploma (or higher) and up to two years in pharmaceutical or sterile manufacturing, with attention to detail and the ability to work in a cleanroom environment and wear PPE.

Qualifications

• High school diploma or equivalent; degree in Pharmacy/Life Sciences preferred.
• 0–2 years in pharmaceutical or sterile manufacturing.
• Knowledge of cGMP and sterile procedures.
• Strong documentation and safety compliance.
• Ability to work in cleanroom and wear PPE.

Responsibilities

• Operate manufacturing equipment per SOPs (e.g., vial filling, sterilization, mixing, labeling).
• Assist in formulation, filling, and inspection of injectable drugs.
• Maintain clean, organized, and safe work area per GMP and OSHA.
• Complete batch records and production documentation.
• Support line clearance, changeovers, and deviations reporting.
• Coordinate with Quality, Engineering and Maintenance.

Skills

cGMP knowledge

GDP knowledge

Sterile manufacturing

Documentation

Communication skills

Cleanroom work

Education

High school diploma or equivalent

Pharmacy/Life Sciences degree

Job description

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Manufacturing Associate

Full Time Chandler, AZ, US

15 days ago Requisition ID: 1129

Salary Range: $45,000.00 To $45,000.00 Annually

Position Summary

The Manufacturing Associate will be responsible for supporting daily operations of the pharmaceutical manufacturing process, ensuring all activities are performed in compliance with cGMP, safety standards, and internal quality systems. The ideal candidate should be detail-oriented, quality-focused, and willing to work in a sterile environment with strict documentation practices.

Key Responsibilities

Operate manufacturing equipment (e.g., vial filling, sterilization, mixing, labeling) as per SOPs.

Assist in the formulation, filling, and inspection of injectable drug products.

Maintain a clean, organized, and safe work area in compliance with GMP and OSHA requirements.

Perform cleaning and sanitization of equipment and manufacturing rooms.

Accurately complete batch records, logbooks, and other production documentation.

Participate in line clearance and changeover activities.

Communicate promptly any deviations, equipment malfunctions, or safety concerns.

Support process improvements and follow instructions from the Production Supervisor.

Work in coordination with the Quality, Engineering, and Maintenance departments.

Qualifications & Skills

High school diploma or equivalent; Diploma or Degree in Pharmacy, Life Sciences, or related field preferred.

0–2 years of experience in pharmaceutical or sterile manufacturing (injectables preferred).

Knowledge of cGMP, GDP, and sterile manufacturing procedures.

Strong attention to detail, documentation, and safety compliance.

Ability to work in a cleanroom environment and wear PPE as required.

Good communication skills and ability to follow written and verbal instructions.

Willingness to work shifts, weekends, or extended hours if needed.