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Manage receipt, inspection, inventory control, and movement of materials in compliance with GMP and regulatory standards. | High school diploma, experience in materials management or warehousing in biotech/pharmaceutical industry, knowledge of GMP, FDA, OSHA regulations, and forklift operation. | Job Title: Material Handler I Location: Rockville, MD Duration: 12-month contract Pay Rate: $20–$27/hr Overview: The Material Handler I will support warehouse operations by managing the receipt, inspection, and movement of materials used in GMP manufacturing. This individual will ensure compliance with all internal procedures and applicable regulations, maintain accurate inventory control, and collaborate with cross-functional teams to ensure timely material flow to manufacturing. Responsibilities: Receive, inspect, and disposition incoming materials to ensure compliance with company, GMP, and regulatory requirements. Ensure accurate inventory control of all controlled materials and execute required cycle counts and inventory reconciliations. Execute material flow and warehouse operations in accordance with SOPs, GMP, FDA, OSHA, IATA, DOT, TSA, and other applicable regulations. Coordinate with Quality Control and Quality Assurance to ensure sampling and release of materials for GMP manufacturing. Operate warehouse equipment, including forklifts and pallet jacks, in a safe manner compliant with OSHA standards. Support shipping, receiving, labeling, and storage of materials as required. Requirements: High School Diploma or equivalent required. Previous experience in materials management, warehousing, or logistics within the biotech or pharmaceutical industry. Working knowledge of GMP, FDA, and OSHA regulations. Ability to operate forklifts and pallet jacks safely; forklift certification preferred. Strong attention to detail, organizational skills, and ability to work in a fast-paced, regulated environment. Ref: #558-Scientific Job Title: Material Handler I Location: Rockville, MD Duration: 12-month contract Pay Rate: $20–$27/hr Overview: The Material Handler I will support warehouse operations by managing the receipt, inspection, and movement of materials used in GMP manufacturing. This individual will ensure compliance with all internal procedures and applicable regulations, maintain accurate inventory control, and collaborate with cross-functional teams to ensure timely material flow to manufacturing. Responsibilities: Receive, inspect, and disposition incoming materials to ensure compliance with company, GMP, and regulatory requirements. Ensure accurate inventory control of all controlled materials and execute required cycle counts and inventory reconciliations. Execute material flow and warehouse operations in accordance with SOPs, GMP, FDA, OSHA, IATA, DOT, TSA, and other applicable regulations. Coordinate with Quality Control and Quality Assurance to ensure sampling and release of materials for GMP manufacturing. Operate warehouse equipment, including forklifts and pallet jacks, in a safe manner compliant with OSHA standards. Support shipping, receiving, labeling, and storage of materials as required. Requirements: High School Diploma or equivalent required. Previous experience in materials management, warehousing, or logistics within the biotech or pharmaceutical industry. Working knowledge of GMP, FDA, and OSHA regulations. Ability to operate forklifts and pallet jacks safely; forklift certification preferred. Strong attention to detail, organizational skills, and ability to work in a fast-paced, regulated environment. Ref: #558-Scientific

Support upstream and downstream biologics manufacturing processes in a GMP environment, including media prep, bioreactor operation, chromatography, filtration, and documentation. | High school diploma with 1-5 years GMP experience or relevant degree, ability to work in sterile environments, and physical ability to lift up to 50 lbs. | Job Title: Manufacturing Associate (Upstream & Downstream) Location: Princeton Area, New Jersey Hours / Schedule: Full-time, shift flexibility required (day, evening, overnight rotation possible, overtime available based on production needs) Type: Temp-to-Hire (potential direct opportunity for the right fit) SUMMARY Support both Upstream and Downstream manufacturing operations in a cGMP-compliant environment. This role provides hands-on experience throughout the biologics production process — from cell culture to protein purification. REQUIREMENTS High School Diploma or Associate’s Degree with 1–5 years of relevant GMP experience OR Bachelor’s Degree in Biotechnology, Biochemistry, Microbiology, Chemical Engineering, or related field 1–5 years of GMP experience in Pharmaceuticals, Biologics, Medical Devices, Cleanroom, or Chemical Processing environments Comfortable working in sterile/cleanroom settings and following strict protocols Strong interest in cross-functional manufacturing roles with growth potential Open to flexible hours outside of a standard 8am–5pm schedule Open to Temp-to-Hire employment Ability to stand for long periods and lift up to 50 lb Strong attention to detail and documentation skills Willingness to cross-train and support evolving production needs Upstream Familiarity with aseptic techniques and bioreactor operation Experience with cell culture, buffer / media prep Downstream Understanding of chromatography, TFF (Tangential Flow Filtration), viral filtration Hands-on experience in cleanroom/purification operations RESPONSIBILITIES Upstream Manufacturing Prepare media and buffers Thaw vials, expand seed trains, and operate bioreactors (fed-batch/perfusion) Monitor/document cell growth and bioreactor parameters Support cell harvest through clarification and filtration Downstream Manufacturing Conduct chromatography operations (AKTA or similar systems) Perform Tangential Flow Filtration (TFF) and diafiltration Execute viral filtration procedures Support cleanroom-based final fill operations General Duties Adhere to cleanroom, gowning, and aseptic protocols Maintain GMP-compliant documentation Clean and sanitize production equipment Collaborate with Quality, Engineering, and Logistics teams #M3 Ref: #558-Scientific Job Title: Manufacturing Associate (Upstream & Downstream) Location: Princeton Area, New Jersey Hours / Schedule: Full-time, shift flexibility required (day, evening, overnight rotation possible, overtime available based on production needs) Type: Temp-to-Hire (potential direct opportunity for the right fit) SUMMARY Support both Upstream and Downstream manufacturing operations in a cGMP-compliant environment. This role provides hands-on experience throughout the biologics production process — from cell culture to protein purification. REQUIREMENTS High School Diploma or Associate’s Degree with 1–5 years of relevant GMP experience OR Bachelor’s Degree in Biotechnology, Biochemistry, Microbiology, Chemical Engineering, or related field 1–5 years of GMP experience in Pharmaceuticals, Biologics, Medical Devices, Cleanroom, or Chemical Processing environments Comfortable working in sterile/cleanroom settings and following strict protocols Strong interest in cross-functional manufacturing roles with growth potential Open to flexible hours outside of a standard 8am–5pm schedule Open to Temp-to-Hire employment Ability to stand for long periods and lift up to 50 lb Strong attention to detail and documentation skills Willingness to cross-train and support evolving production needs Upstream Familiarity with aseptic techniques and bioreactor operation Experience with cell culture, buffer / media prep Downstream Understanding of chromatography, TFF (Tangential Flow Filtration), viral filtration Hands-on experience in cleanroom/purification operations RESPONSIBILITIES Upstream Manufacturing Prepare media and buffers Thaw vials, expand seed trains, and operate bioreactors (fed-batch/perfusion) Monitor/document cell growth and bioreactor parameters Support cell harvest through clarification and filtration Downstream Manufacturing Conduct chromatography operations (AKTA or similar systems) Perform Tangential Flow Filtration (TFF) and diafiltration Execute viral filtration procedures Support cleanroom-based final fill operations General Duties Adhere to cleanroom, gowning, and aseptic protocols Maintain GMP-compliant documentation Clean and sanitize production equipment Collaborate with Quality, Engineering, and Logistics teams #M3 Ref: #558-Scientific

Troubleshoot and maintain automated manufacturing equipment, optimize processes, support projects, and conduct preventive maintenance. | 2-4 years technical experience in automation or high-speed systems, PLC programming skills, mechanical/electrical troubleshooting, 3D modeling experience, and ability to work in cleanroom environments. | Job Title: Automation Engineering Technician Location: Littleton, CO Salary: $30.00-$38.00/hour + shift differential + bonus Type: Direct Hire, Full-Time Shifts: Days of the Week Available: Sunday - Tuesday and Every Other Wednesday or Thursday – Saturday and Every Other Wednesday Hours Choices: Day Shift and Shifts for Night Owls! Day Shift Choice 5:30 AM - 6:00 PM or Overnight Choice 5:30 PM – 6:00 AM Overview Are you a skilled Automation Engineering Technician looking to take your career to the next level in a dynamic and high-tech environment? We are seeking an experienced technician to support the production of cutting-edge medical technologies that improve patient care globally. In this role, you’ll troubleshoot advanced automated systems, drive continuous improvement initiatives, and work with state-of-the-art equipment, all while collaborating with engineers and a passionate team. Responsibilities • Advanced Troubleshooting (40%) Provide expert troubleshooting for automated manufacturing equipment, including mechanical, electrical, pneumatic, hydraulic, and control systems. Use PLC ladder logic to resolve machine control issues and ensure minimal downtime. • Process Optimization & Project Support (30%) Partner with engineering to execute process validations and help develop solutions that improve overall equipment efficiency (OEE). You’ll also contribute to design reviews, URS, PFMEAs, and testing during new automation projects. • Preventive Maintenance & Data Analysis (30%) Conduct preventive maintenance on automated systems and monitor machine data to identify trends, proactively solve problems, and optimize production performance. This is your chance to make a real impact on process improvements and reduce maintenance costs. Qualifications • 2–4 years in a technical role (preferably in automation or high-speed systems). • Experience with RF welding applications, cam automation, or GMP-regulated environments is a plus. • Hands-on experience with PLC programming (Allen Bradley or Siemens), Vision systems (Cognex), and networking (Ethernet, DeviceNet, DH485, etc.). • Proficient in troubleshooting mechanical, electrical, hydraulic, and pneumatic systems. • Experience with 3D modeling software (SolidWorks/Solid Edge) for equipment design. • Ability to perform root cause analysis and implement improvements. • Ability to lift up to 50 pounds and work in a cleanroom environment. • Two-year technical degree or equivalent education/experience in an automation or technical role. Additional Perks • Comprehensive Benefits: Medical, dental, and vision plans. • Wellness Program: Robust offerings to support your health and well-being. • 401(k): Company match to support your future planning. • PTO: Generous vacation and sick time to ensure you have time for yourself. • Bonus: Annual bonus potential of 7% based on performance. #M3 Ref: #558-Scientific