Archived listing. The details below describe a past opening.
Job Title: Packaging Technician / Production TechnicianJob DescriptionThe Packaging Technician supports visual inspection and secondary and tertiary packaging activities for parenteral products at various stages of development at a new, state-of-the-art manufacturing site in Nashville, TN. In this role, you help qualify and start up a new aseptic formulation and filling facility, ensuring all visual inspection and packaging operations comply with regulatory requirements, current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs). You work across multiple packaging formats to maintain high standards of safety, quality, and compliance in an FDA-regulated environment.Responsibilities
- Perform visual inspection of vials, syringes, IV bags, cream containers, and other parenteral products to identify defects and ensure product quality.
- Carry out secondary and tertiary packaging operations in accordance with cGMP, SOPs, and regulatory requirements.
- Set up and operate packaging equipment, including labelers, cartoning equipment, and serialization stations, ensuring proper line clearance and readiness for production.
- Document all packaging and inspection activities accurately and completely within batch records, protocols, and other required documentation.
- Ensure packaging operations meet or exceed site safety, quality, and compliance metrics while following all site standards, policies, and procedures.
- Support equipment validation and qualification activities related to packaging and inspection equipment.
- Assist with troubleshooting packaging equipment and processes to minimize downtime and maintain efficient operations.
- Support training activities by following established procedures and sharing knowledge with team members as appropriate.
- Assist Maintenance personnel with preventive maintenance and calibration activities on packaging and inspection equipment as needed.
- Participate in continuous improvement initiatives for the packaging area, including investigations, corrective and preventive actions (CAPA), and process optimization efforts.
- Follow all relevant Standard Operating Procedures (SOPs), Work Instructions, and cGMP requirements at all times.
- Collaborate with cross-functional team members in a fast-paced, collaborative environment to meet production schedules and quality targets.
- Maintain a clean, organized, and compliant work area within the cleanroom and packaging environments.
Essential Skills
- 1+ years of experience working in a pharmaceutical, production, or other regulated environment is preferred.
- Experience with visual inspection, sterile packaging, clinical trial packaging, or related manufacturing activities is preferred.
- Demonstrated ability to perform detailed visual inspection of vials, syringes, IV bags, and similar containers to identify defects.
- Working knowledge of cGMP principles and regulatory expectations in an FDA-regulated environment.
- Good documentation skills with the ability to accurately complete batch records, protocols, and other manufacturing documents.
- Strong attention to detail and commitment to quality and compliance.
- Ability to work effectively in a team-oriented environment.
- Good interpersonal skills and a self-motivated, proactive work style.
- Strong learning agility with the ability to quickly understand new processes, equipment, and procedures.
- Ability to perform in a fast-paced, collaborative production environment.
- Excellent written and verbal communication skills.
Additional Skills & Qualifications
- Prior experience in pharmaceutical manufacturing, sterile packaging, or clinical trial packaging.
- Experience working in a cleanroom or other controlled environment.
- Familiarity with equipment validation, qualification, and troubleshooting in a production setting.
- Exposure to continuous improvement initiatives, investigations, and CAPA processes.
- Experience as a pharmacy technician or similar role in a regulated healthcare or manufacturing environment.
- Comfort with following detailed SOPs, Work Instructions, and documentation practices.
- Ability to work across different shifts as needed by production demands.
Why Work Here?You will join a growing organization that is investing significantly in a two-phase expansion project, including a new state-of-the-art medical manufacturing facility adjacent to the current site. The work directly contributes to global health by supporting the production of critical parenteral products in an FDA-regulated environment. You gain exposure to cutting-edge aseptic formulation and filling operations, with opportunities to grow your skills in cGMP manufacturing, equipment qualification, and continuous improvement. The culture emphasizes collaboration, learning, and advancement, offering dynamic career paths for those who want to develop professionally while making a meaningful impact.Work EnvironmentYou work in a clean, state-of-the-art FDA-regulated medical manufacturing facility in Nashville, TN, focused on aseptic formulation, filling, and packaging of parenteral products. The environment includes cleanroom and controlled areas where you perform visual inspection and packaging operations using equipment such as labelers, cartoning machines, and serialization stations. Multiple shifts are available: 1st shift from 7:00 a.m. to 3:30 p.m. Monday through Friday, 2nd shift from 3:00 p.m. to 11:30 p.m. Monday through Friday, and 3rd shift from 11:00 p.m. to 7:30 a.m. Sunday through Thursday. Work follows cGMP standards with a strong focus on safety, quality, and compliance. The role requires wearing full cleanroom personal protective equipment (PPE) and following an in-depth gowning process for entry into controlled areas. The facility supports a structured, process-driven, and highly regulated environment where clear documentation and adherence to SOPs are essential. Job Type & LocationThis is a Contract to Hire position based out of Nashville, TN. Pay and BenefitsThe pay range for this position is $22.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Workplace TypeThis is a fully onsite position in Nashville,TN. Application DeadlineThis position is anticipated to close on Oct 16, 2026.
About Aerotek
Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.