Senior Aseptic Manufacturing Technician

PCI Pharma Services; Bedford (AL); On-site; USD 60,000 - 85,000; Full time

Job summary

PCI Pharma Services is hiring a Manufacturing Technician III in Alabama to perform aseptic filling, lyophilization, and related operations under GMP guidelines. You will train peers, resolve process issues, and ensure compliance with safety and quality standards.

Ideal candidates have 3–5 years in pharma or medical device environments, strong aseptic skills, and experience with controlled documents. Responsibilities include equipment prep, batch records, and SOP adherence to support scalable

Qualifications

• 3–5 years of working experience in the pharmaceutical or medical device industry.
• Strong knowledge of aseptic techniques and fill finish experience required.
• Experience in reviewing and creating controlled documents.
• Requires a high school diploma with 4+ years of cGMP Pharmaceutical experience to include finished dose form.
• Ability to weigh and measure raw materials and operate basic benchtop instruments.

Responsibilities

• Maintains safe work habits and adheres to PCI safety procedures.
• Mentors less experienced staff in aseptic techniques.
• Prepares solutions, aseptic filling and labeling of vials under sterile and non-sterile conditions.
• Operates aseptic filling and lyophilizer equipment in cleanroom environments.
• Prepares equipment for sterilization and Lyophilization.
• Operates processing equipment including autoclaves, ovens and depyrogenation steps.
• Completes and maintains batch records and documentation.

Skills

Aseptic techniques

Fill finish experience

Documentation control

Equipment operation

Troubleshooting

Education

High school diploma with 4+ years cGMP experience

Tools

Aseptic filling equipment

Lyophilizer

Autoclaves

Job description

PCI Pharma Services is hiring a Manufacturing Technician III in Alabama to perform aseptic filling, lyophilization, and related operations under GMP guidelines. You will train peers, resolve process issues, and ensure compliance with safety and quality standards.

Ideal candidates have 3–5 years in pharma or medical device environments, strong aseptic skills, and experience with controlled documents. Responsibilities include equipment prep, batch records, and SOP adherence to support scalable