Manufacturing Associate (2nd Shift)

Manufacturing Associate (2nd Shift)

Manufacturing

Wilmington, Ohio, US

• Added - 04/08/2026

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 (2 nd 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

INDBH

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.