FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in sterile manufacturing operations, including aseptic techniques and cGMP compliance, while effectively performing calculations and operating production equipment. Proficient in handling raw materials and maintaining product sterility throughout the manufacturing process.
Highest-signal resume keywords
Sterile Manufacturing OperationsAseptic TechniquesCGMP ComplianceProduct ProcessingMechanical Aptitude
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Product FormulationCalculations and ConversionsHazardous Waste HandlingDecontamination MethodsSterilization TechniquesBasic Laboratory PracticesBiology KnowledgeMicrobiology KnowledgeManufacturing Systems UnderstandingEquipment Operation
Tools & Technologies
Production EquipmentComputer Software
Industry Keywords
SOPsCGMP DocumentationParenteral ProductsFinal Product FormulationsAseptic Processing Practices
About the role
Key responsibilities & impact- Support sterile manufacturing operations by filling antigen serials and preparing final product formulations
- Independently perform product processing according to SOPs, Manufacturing Directions, cGMP requirements, and aseptic techniques
- Manufacture and compound sterile solutions and other parenteral products
- Obtain, weigh, measure, and add raw materials according to production procedures
- Set up, operate, inspect, and dismantle production equipment for cleaning
- Assess equipment and materials for readiness before use
- Assemble antigens into final product formulations
- Prepare adjuvants and other intermediates while maintaining product sterility
- Verify and document component identities in accordance with cGMP documentation requirements
- Follow SOPs, Filling Manufacturing Directions, and established aseptic processing practices
Requirements
What you’ll need- High School Diploma or GED
- Experience working in a manufacturing, production, laboratory, or similar regulated environment preferred
- Ability to perform calculations and conversions involving weights, volumes, and percentages
- Computer aptitude with the ability to learn and adapt to new platforms and software
- Knowledge of hazardous waste handling, decontamination, sterilization, and BPE methods preferred
- Understanding of basic cGMP and documentation practices preferred
- Knowledge of basic laboratory practices, biology, and microbiology preferred
- Understanding of aseptic manufacturing or processing environments preferred
- Mechanical aptitude with an understanding of manufacturing systems, equipment, and processes preferred
- Ability to lift up to 50 lbs
- Ability to work the stated overnight schedule, Sunday through Thursday, 10:00 pm–6:30 am
Benefits
Comp & perks- Overtime may be required based on production demands
- Ability to lift up to 50 lbs
- Diverse and inclusive work environment
- New skills and experiences for career development
- Equal employment opportunity and affirmative action workplace
