Manufacturing Associate (2nd Shift)

Astrix; Wilmington (OH); On-site; USD 29,000 - 30,000; Full time

Job summary

Astrix in Wilmington, OH is seeking a Manufacturing Associate I (2nd Shift) to support sterile pharmaceutical production in a cGMP environment. The role involves equipment prep, aseptic processing, documentation, and batch execution in a fast-paced facility.

The ideal candidate will be detail-oriented, dependable, and eager to learn while adhering to quality and safety standards. Onsite work Mon-Thur 3pm-1:30am with potential for contract-to-hire advancement and weekend coverage as needed.

Qualifications

• High School Diploma or GED required.
• 0–1 year of experience in sterile pharmaceutical or GMP manufacturing.
• Associate degree or higher in science or technical discipline.
• Knowledge of aseptic manufacturing principles.
• Familiarity with cGMP, HAZCOM, RCRA, and general manufacturing safety requirements.

Responsibilities

• Perform equipment cleaning, assembly, setup, and operation for manufacturing processes.
• Execute batch processing activities for sterile microsphere, suspension, and liquid products.
• Read, understand, and accurately follow SOPs, Master Production Records (MPRs), and manufacturing procedures.
• Complete cGMP documentation accurately and in a timely manner.
• Monitor manufacturing processes with close attention to detail.
• Perform aseptic gowning and maintain gowning qualification.
• Conduct cleanroom and manufacturing area sanitization activities.
• Assist with equipment preparation and changeovers.
• Support process development and validation activities as needed.
• Follow all company policies, quality standards, and safety procedures.
• Perform additional duties as assigned by management.
• Provide shift and occasional weekend coverage when required.

Skills

Detail-oriented

Documentation practices

Teamwork

Strong communication

Adaptability

Fast learner

Education

High School Diploma or GED

Associate degree or higher in science/technical

Tools

HMI systems

Autoclaves

Job description

Pay Rate Low: 21 | Pay Rate High: 22

Our client is seeking a detail-oriented Manufacturing Associate to join its sterile pharmaceutical manufacturing team, supporting the production of high-quality microsphere, suspension, and liquid products in a regulated cGMP environment.

Title: Manufacturing Associate I (2nd Shift) – Multiple Openings

Location: Wilmington, OH (Onsite)

Schedule: Mon-Thur 3pm-1:30am (4x10)

Pay Rate: $21/hr - $22/hr

Employment Type: Contract-to-Hire

Position Summary

This role is responsible for performing manufacturing operations in a cGMP-regulated cleanroom environment, including equipment preparation, aseptic processing, documentation, and batch execution.

The ideal candidate is detail-oriented, dependable, eager to learn, and comfortable working in a fast-paced manufacturing environment while maintaining strict quality and safety standards.

Key Responsibilities

• Perform equipment cleaning, assembly, setup, and operation for manufacturing processes.


• Execute batch processing activities for sterile microsphere, suspension, and liquid products.


• Read, understand, and accurately follow SOPs, Master Production Records (MPRs), and manufacturing procedures.


• Complete cGMP documentation accurately and in a timely manner.


• Monitor manufacturing processes with close attention to detail.


• Perform aseptic gowning and maintain gowning qualification.


• Conduct cleanroom and manufacturing area sanitization activities.


• Assist with equipment preparation and changeovers.


• Support process development and validation activities as needed.


• Follow all company policies, quality standards, and safety procedures.


• Perform additional duties as assigned by management.


• Provide shift and occasional weekend coverage when required.

Required Qualifications

• High School Diploma or GED required.


• Ability to work onsite on a Monday–Thursday overnight schedule.


• 0–1 year of experience in sterile pharmaceutical or GMP manufacturing.


• Associate degree or higher in a science or technical discipline.


• Knowledge of aseptic manufacturing principles.


• Familiarity with Current Good Manufacturing Practices (cGMP), HAZCOM, RCRA, and general manufacturing safety requirements.

Desired Skills & Attributes

• Positive attitude and strong work ethic


• High level of integrity and accountability


• Dependable and self-motivated


• Detail-oriented with excellent documentation practices


• Adaptable in a changing production environment


• Quick learner with a willingness to develop new skills


• Strong communication and teamwork skills


• Ability to prioritize tasks and respond quickly to production needs

Physical Requirements

• Ability to work in a sterile cleanroom while wearing full aseptic gowning, including hood, coveralls, boots, mask, goggles, and gloves.


• Maintain annual aseptic gowning qualification.


• Ability to stand for up to 7 hours while wearing steel-toed shoes.


• Frequent walking, bending, reaching, climbing, pushing, and pulling carts.


• Ability to operate manufacturing equipment, including HMI systems and autoclaves.


• Ability to lift up to 50 pounds independently and participate in team lifts up to 100 pounds.


• Ability to perform repetitive tasks throughout the shift.

Why Join Us?

• Contract-to-hire opportunity with long-term career potential


• Stable Monday–Thursday schedule with three-day weekends


• Hands-on experience in sterile pharmaceutical manufacturing


• Opportunity to develop GMP and aseptic manufacturing expertise


• Collaborative, safety-focused team environment