Biopharm Manufacturing Assoc

Biopharmaceutical Manufacturing Associate

Location: Rockville, MD

Pay Rate: $22-$23/hour

Contract: 18 months with potential for conversion to full-time employment

Openings: 7

Alphanumeric is hiring Biopharmaceutical Manufacturing Associates to work onsite in Rockville, MD with our long-standing life sciences client committed to improving lives through medical and pharmaceutical advancements.

This is an excellent opportunity for early-career candidates interested in building a career in biopharmaceutical manufacturing. Previous pharmaceutical or biotechnology manufacturing experience is preferred but not required; candidates with the right education, reliability, attention to detail, and willingness to learn are encouraged to apply.

Training & Work Schedule

Selected candidates will complete approximately 6 weeks of training, Monday-Friday, 9:00 AM-5:00 PM.

Following training, associates must be willing and able to work a 12-hour shift schedule, which may include:

• Day Shift: 6:00 AM-6:00 PM
• Night Shift: 6:00 PM-6:00 AM
• Weekend and rotating shift coverage as required

Key Responsibilities

As a Biopharmaceutical Manufacturing Associate, you will support the production of high-quality biopharmaceutical drug substance in a safe, compliant, and reliable manufacturing environment.

Responsibilities include:

• Prepare, clean, sterilize, batch, pasteurize, filter, and deliver media and solutions used in cell culture and purification operations.
• Set up, operate, clean, and break down manufacturing/process equipment.
• Perform sampling procedures and use analytical instruments to evaluate cell culture, solutions, and product characteristics.
• Operate filter-integrity equipment to confirm filter integrity before and after use.
• Monitor manufacturing processes, equipment, and instrumentation and escalate potential issues appropriately.
• Set up fixed and mobile process equipment with CIP (Clean-in-Place) systems to perform validated cleaning and sterilization processes.
• Follow established SOPs, protocols, batch records, and logbooks.
• Maintain accurate documentation in accordance with Good Documentation Practices and data-integrity requirements.
• Follow all applicable safety policies and actively contribute to a strong safety culture.