Manufacturing Technician III

Job Description

Job Description

Job Title: Manufacturing Technician III

Job Description

The Manufacturing Technician III is responsible for results in a fast-paced environment, assisting with the manufacturing of sterile injectable products in vial and syringe configurations for clinical and commercial distribution. This key role oversees and executes advanced production tasks involving compound, fill, and finish processes for sterile injectable pharmaceutical products using aseptic isolator technology. This position requires a high level of technical expertise in aseptic processes, leadership in troubleshooting, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The technician operates manufacturing processing equipment by following standard operating procedures (SOPs) and batch records, ensuring compliance with regulatory agencies and current Good Manufacturing Practices (cGMPs).

Responsibilities

• Perform complex manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection.
• Serve as a subject matter expert on compounding and filling processes and equipment, providing guidance and training to other manufacturing employees.
• Monitor production processes to ensure adherence to SOPs, batch records, and quality standards, making real-time adjustments to maintain product quality.
• Troubleshoot and resolve complex equipment and process issues, minimizing downtime and ensuring efficient production flow.
• Conduct in-process and end-of-process sampling and quality checks, ensuring all manufactured products meet rigorous standards.
• Collaborate with cross-functional teams on continuous improvement initiatives to enhance product quality, safety, and efficiency.
• Act as an active team member that enacts ideas and incorporates them as part of manufacturing readiness and execution.
• Assist with the validation and qualification of new equipment and processes, ensuring seamless integration into the production workflow.
• Maintain accurate and detailed production documentation, completing documentation with minimum errors and escalating recommendations for revisions.
• Follow applicable SOPs and cGMPs to perform assigned duties and tasks.
• Ensure timely completion and compliance with cGMP and all other relevant company training requirements.
• Document activities legibly in real time on controlled documentation per SOPs and cGMPs.
• Perform in-process sampling, weight checks, component counting, and basic math calculations.
• Perform in-process inspection and finished product visual inspection.
• Clean rooms, tools, and equipment before and after use.
• Assist with other manufacturing areas as required.
• Perform activities right the first time in areas of material handling, dispensing, compounding, and filling.
• Follow general instructions on routine work and detailed instructions on new projects or assignments.
• Follow all Safety requirements and lead by example a safety-first culture.
• Work occasional hours outside of scheduled shift based on business needs, which may include weekend work.

Essential Skills

• 4-6+ years of relevant experience in sterile/aseptic manufacturing or Drug Substance manufacturing.
• Experience in a cGMP pharmaceutical manufacturing environment.
• 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.
• Excellent verbal and written communication skills.
• Ability to execute tasks with minimum oversight while guiding the team.
• Strong detail orientation and organizational skills.
• Basic computer skills (Microsoft Office) and familiarity with electronic documentation systems.

Additional Skills & Qualifications

• High school diploma or GED required; Associate’s or Bachelor’s degree preferred.
• Prior pharmaceutical or CDMO experience required.
• Ability to read and comprehend detailed written instructions and apply instructions during execution.
• Capability to move materials throughout the facility using appropriate methods and equipment.
• Ability to use appropriate PPE based on product (e.g., PAPR, Supplied Air Respirator).

Work Environment

This is a 100% on-site position. The working hours are on the 3rd Shift, Sunday through Thursday, from 11:00 pm to 7:30 am. The position requires working in a controlled environment with strict adherence to safety and aseptic techniques, including the use of personal protective equipment (PPE).

This is a Permanent position based out of Morrisville, NC.

The pay range for this position is $62400.00 - $79040.00/yr.

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.

This is a fully onsite position in Morrisville,NC.

This position is anticipated to close on Apr 17, 2026.

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.