Pay Rate Low: 20 | Pay Rate High: 22

Position Overview

We are partnering with a growing biopharmaceutical manufacturing facility to place a motivated Downstream Manufacturing Associate on a collaborative production team. This is a great entry-level opportunity for someone with a foundational background in life sciences or cGMP manufacturing who is eager to build their skills in a structured, regulated environment. The ideal candidate brings a quality-first mindset, strong attention to detail, and the ability to thrive within a highly proceduralized, team-oriented setting.

Shift: Sunday–Wednesday | 2nd Shift Sun–Tue: 3:00 PM – 1:30 AM | Wed: 3:00 PM – 11:30 PM Hours: 38 hrs/week Type: Contract (Est. Start: May 2026 | Est. End: September 2026)

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What You'll Do

• Carry out core downstream manufacturing unit operations including parts cleaning, weighing and dispensing, equipment preparation, kit assembly, and material staging.
• Assist with cleaning-in-place (CIP) and sterilization-in-place (SIP) of tanks and process equipment under the guidance of qualified personnel.
• Support buffer preparation and the transfer of materials into tanks and bags.
• Provide internal support by replenishing consumables, maintaining controlled document binders, and properly disposing of expired reagents.
• Identify and report any process or equipment irregularities in a timely manner.
• Document all work in accordance with cGMP and cGDP standards.
• Maintain production spaces to predefined cleanliness and organization standards (5S).
• Adhere to all applicable safety protocols and escalate unsafe conditions or behaviors as appropriate.

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What We're Looking For

• High school diploma or equivalent required; associate's/bachelor's degree or biotechnology/vocational training preferred.
• 1+ year of experience in a cGMP-regulated environment is a plus; entry-level candidates with relevant training will be considered.
• Demonstrated ability to focus on detail-oriented, repetitive tasks with a quality and "right the first time" mindset.
• Comfortable working within a highly regulated setting, following SOPs, operational control procedures, and compliance guidelines.
• Ability to read, understand, and execute written work instructions and document work per cGMP standards.
• Willingness to work within a 24/7 shift structure and adapt scheduling with appropriate notice.

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This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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