Manufacturing Technician II - Sterile Injection - 12-Hr Day Shift 2-2-3
Alcami Corporation
Summary
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology.
Job description
Job Summary
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology.
On-Site Expectations
100% on-site position. Day Shift: 12-Hour Rotating (2-2-3), 7:00am - 7:00pm.
Responsibilities
- Learns and executes manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection.
- Become a subject matter expert (SME) on compounding/filling processes and equipment.
- Performs production processes with adherence to SOPs, batch records, quality standards, and minimally contributes deviations to maintain product quality.
- Conducts in-process and end-of-process sampling/quality checks, ensuring all manufactured products meet rigorous standards.
- Identifies inefficiencies and escalates to area supervision real-time to support continuous process improvement.
- Maintains accurate and detailed production documentation.
- Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
- Performs in-process sampling, weight checks, and component counting and basic math calculations.
- Performs in-process inspection and finished product visual inspection.
- Performs cleaning of rooms, tools, and equipment before and after use.
- Assists with other manufacturing areas as required.
- Follows all Safety requirements and leads by example a safety-first culture.
- Works occasional hours outside of scheduled shift based on business needs, which may include weekend work.
Manufacturing Technologies for Sterile Liquids
- Equipment and component preparation and sterilization (i.e., filter integrity testing, autoclaving, parts wrapping)
- Compounding
- Vial Washing / Depyrogenation
- Aseptic Filling / Stoppering / Capping
- Lyophilization
- Visual Inspection
- Facility Cleaning/Sanitation
- Documentation Review (Batch Record, Logbooks, etc.)
Requirements
- High school diploma or GED required
- Associate or bachelor's degree preferred
- 1-2 years' work experience required; 2-5 years preferred
- Prior work experience in a cGMP pharmaceutical manufacturing environment required
- Previous experience in dispensing, compounding, aseptic filling, or visual inspection highly desirable
- Candidates with life sciences or engineering degrees will be considered without manufacturing experience
- Excellent verbal and written communication skills
- Proven ability to operate, troubleshoot, and maintain complex manufacturing equipment
- Strong detail orientation and organizational skills required
- Strong problem-solving and basic trouble-shooting ability required
- Ability to perform basic math calculations
- Ability to read and comprehend detailed written instructions
- Ability to move materials throughout the facility using appropriate methods and equipment
- Ability to use appropriate PPE based on product handling requirements
- Strong attention to detail and ability to detect minute defects
- Excellent communication and interpersonal skills
- Ability to work independently and collaboratively in a fast-paced environment
- Flexibility to adapt to changing priorities
- Basic computer skills (Microsoft Office) and familiarity with electronic documentation systems preferred
Company overview
Alcami Corporation is a leading US-based contract development and manufacturing organization (CDMO) with over 45 years of experience in advancing pharmaceuticals and biologics from development to commercial delivery. Headquartered in North Carolina, the company operates six campuses strategically located near major pharmaceutical and biotech hubs across the United States. Alcami provides comprehensive, integrated solutions including analytical development and testing services, drug product manufacturing for both oral solid dose and sterile parenteral products, cGMP pharmaceutical storage, and support services such as environmental monitoring, calibration, and validation. With more than 1,000 employees and 770,000 square feet of operational space, Alcami serves pharmaceutical and biotechnology companies of all sizes, from virtual startups to large established organizations. The company's expertise spans small and large molecules, complex formulations, and DEA-scheduled drug products, offering end-to-end solutions that support clients through every stage of the development lifecycle.