Manufacturing Technician III - Sterile Injection - 12-Hr Night Shift 2-2-3

NCBioImpact; Morrisville (NC); On-site; USD 52,000 - 76,000; Full time

Job summary

Alcami is seeking a Manufacturing Technician III for the Sterile Liquids division on a 12‑hour night shift (2‑2‑3) in Morrisville, NC. This role focuses on aseptic processing, fill/finish, and QA documentation within a cGMP environment.

You will lead with expertise, train peers, and ensure regulatory compliance across setup, operation, and validation activities. The position emphasizes hands-on manufacturing, documentation integrity, and continuous improvement while adhering to PPE protocols and

Qualifications

• 4–6+ years of sterile/aseptic manufacturing experience.
• Experience in cGMP pharmaceutical manufacturing environments.
• Prior CDMO experience.
• Strong attention to detail and documentation discipline.

Responsibilities

• Perform setup, operation, and maintenance of equipment used in dispensing, compounding, filling and inspection.
• Act as SME on compounding/filling processes and train other staff.
• Monitor processes for SOP and batch record compliance and adjust as needed.
• Troubleshoot equipment/process issues to minimize downtime.
• Conduct in-process and end-of-process sampling and quality checks.

Skills

Verbal and written communication

Operational troubleshooting

Equipment operation

Documentation & record keeping

Basic computer skills

Mentoring/train others

Education

High school diploma or GED

Associate’s or Bachelor’s degree preferred

Job description

Manufacturing Technician III - Sterile Injection - 12-Hr Night Shift 2-2-3

Location: US-NC-Morrisville

ID: 2026-2469

Category: Manufacturing

Position Type: Full-Time

Working Hours: Night Shift: 12-Hour Rotating (2-2-3), 7:00pm - 7:00am

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Manufacturing Technician III (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 Technician III is a key role responsible for overseeing and executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, leadership in troubleshooting, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Technician III performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician III employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician III demonstrates technical ability in applicable functional areas including department procedures, troubleshooting/problem solving, manufacturing document revision, and training/coaching other technicians. The position requires the ability to convey new processes and techniques to other team members to support the manufacturing department.

On-Site Expectations

• 100% on-site position.
• Night Shift: 12-Hour Rotating (2-2-3), 7:00pm - 7:00am.

Responsibilities

• Performs complex manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection.
• Serves as a subject matter expert (SME) on compounding/filling processes and equipment, providing guidance and training to other manufacturing employees.
• Monitors production processes to ensure adherence to SOPs, batch records, and quality standards, making real-time adjustments to maintain product quality.
• Troubleshoots and resolves complex equipment and process issues, minimizing downtime and ensuring efficient production flow.
• Conducts in-process and end-of-process sampling/quality checks, ensuring all manufactured products meet rigorous standards.
• Collaborates with cross-functional teams (e.g., Manufacturing Specialists, Technical Services, Quality Assurance, Engineering, etc.) on continuous improvement initiatives to enhance product quality, safety, and efficiency.
• Is an active team member that enacts ideas and incorporates them as part of manufacturing readiness and execution.
• Employee is first to volunteer and largely contributes to performance of the team.
• Assists with the validation and qualification of new equipment and processes, ensuring seamless integration into the production workflow.
• Maintains accurate and detailed production documentation. Documentation is completed with minimum errors and recommendations are escalated to drive document revisions to reduce errors.
• Follows applicable SOPs and cGMPs to perform assigned duties and tasks.
• Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
• Legibly documents activities in real time on controlled documentation per SOPs and cGMPs.
• 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.
• Performs activities right first time in areas of material handling/dispensing, compounding, and filling.
• Follows general instructions on routine work and detailed instructions on new projects or assignments.
• Follows all Safety requirements and leads by example a safety-first culture.
• Assists with other manufacturing areas as required.
• Works occasional hours outside of scheduled shift based on business needs, which may include weekend work.
• Other duties as assigned.

Manufacturing Technologies for Sterile Liquids (including but may not be limited to):

• 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.)

Qualifications

• High school diploma or GED required.
• Associate’s or Bachelor’s degree preferred.
• 4-6+ years of relevant experience required, with a strong background in sterile/aseptic manufacturing or Drug Substance manufacturing.
• Prior work experience in a cGMP pharmaceutical manufacturing environment required.
• Prior pharmaceutical or CDMO experience required.

Knowledge, Skills, and Abilities

• Capable of executing tasks with minimum oversight while giving guidance to team to ensure manufacturing success.
• Excellent verbal and written communication skills, works collaboratively in a team environment and stands in for Lead during shift exchange.
• Proven ability to operate, troubleshoot, and maintain complex manufacturing equipment.
• Demonstrated leadership skills, with experience training and mentoring team members.
• Strong analytical and problem-solving skills with a focus on detail and accuracy.
• Applies job skills, company policies and SOPs to complete a variety of assignments.
• Strong detail orientation and organizational skills required.
• Strong problem-solving and basic trouble‑shooting ability required.
• Ability to train others effectively.
• Ability to perform basic math calculations.
• Ability to read and comprehend detailed written instructions and apply instructions during execution is required.
• Ability to move materials throughout the facility using appropriate methods and equipment required.
• Ability to use the appropriate PPE based on product (i.e. PAPR, Supplied Air Respirator).
• Basic computer skills (Microsoft Office) and familiarity with electronic documentation systems is required.

Travel Expectations

• Up to 5% domestic travel.

Physical Demands and Work Environment

The physical demands and work environment characteristics described here are representative of those that must be met or encountered by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to walk; climb or balance and stoop, kneel, crouch, or crawl. The employee is occasionally required to sit. The employee must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, occasionally lift and/or move up to 75 pounds and occasionally lift and/or move over 75 pounds with assistance. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. The employee must have 20/20 vision (with or without corrective lenses) and must possess the ability to pass a color‑blind test.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. The use of tight‑fitting respirators limits facial hair for proper protection. Based on product, the use of PAPR or supplied air respirator may be required. Regulations may require employees to participate in routine medical surveillance. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle such as a forklift.

About Us

Alcami is a contract development and manufacturing organization headquartered in North Carolina with over 40 years of experience advancing products through every stage of the development lifecycle. At Alcami, we are a team of dynamic, agile individuals committed to developing life‑saving drugs around the world. A mindset of collaboration, innovation, responsiveness, accountability, and customer focus inspires us to be the most efficient, safe, and reliable choice for our customers and the patients they serve. In return, we offer challenging careers, professional growth, and the opportunity to be part of our skilled team with over 40 years of experience as champions that are dedicated, trustworthy, and relentless to advancing products through every stage of the development cycle. Alcami offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision and prescription coverage, life, LTD, STD, 401(k) with match and immediate vesting, and tuition reimbursement / student loan forgiveness.

Diversity and Inclusion

Alcami is an Equal Opportunity / Aff employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.