Biopharma Manufacturing Associate III – Production Support

Bora Pharmaceuticals; Rockville (MD); On-site; USD 88,000 - 115,000; Full time

Benefits offered by this job

Competitive compensation

Health insurance

401(k) with match

Paid time off

Professional development

Wellness programs

EAP & mental health

Job summary

Bora Pharmaceuticals is seeking a Manufacturing Associate III - Production Support to help prepare solutions for biologics production in a cGMP setting. The role supports clinical programs by ensuring materials meet specifications and regulatory requirements.

Responsibilities include weigh/dispense, buffer/media prep, cleaning, equipment use, and drafting SOPs while maintaining accurate records and collaborating with QA/QC for quality goals. Strong GMP experience is essential.

Qualifications

• Minimum education and experience requirements for FDA regulated biopharmaceutical manufacturing environments.
• Experience following GMP rules and procedures is required.
• Strong ability to document, revise technical notes and reports clearly.

Responsibilities

• Assist manufacturing of material for clinical trials in GMP environment, including weigh/dispense, buffer prep, media prep, cleaning, and material ordering.
• Operate bioprocess equipment and maintain calibration.
• Prepare materials for cleanroom use and document activities per SOPs and GMP.
• Draft and revise GMP documents; write deviation/incident reports as needed.
• Coordinate with QA/QC for sample testing, room release and quality goals.

Skills

Chemistry knowledge

Mentoring

Teamwork

Attention to detail

Technical writing

Mathematical calculations

Equipment operation

Critical thinking

Continuous improvement

Independent learner

Manual dexterity

Interpersonal skills

Overtime flexibility

Lifting 30 lbs

Education

High School Diploma or equivalent with 5 years biopharma exp

Associate's degree with 4 years exp

Bachelor's degree with 3 years exp

Tools

Excel

Word

PowerPoint

Job description

Bora Pharmaceuticals is seeking a Manufacturing Associate III - Production Support to help prepare solutions for biologics production in a cGMP setting. The role supports clinical programs by ensuring materials meet specifications and regulatory requirements.

Responsibilities include weigh/dispense, buffer/media prep, cleaning, equipment use, and drafting SOPs while maintaining accurate records and collaborating with QA/QC for quality goals. Strong GMP experience is essential.