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Packaging Technician

  • Nashville, TN, United States

$22 to $23 USD / hour

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Job details

Pay
$22 to $23 USD / hour
Posting language
English
Posted

Original job description

Packaging TechnicianJob DescriptionThe Packaging Technician supports visual inspection, secondary packaging, and tertiary packaging activities for parenteral products at various stages of development at a Nashville, TN manufacturing site. This role offers an opportunity to contribute to the qualification and start-up of a new aseptic formulation and filling facility, helping to establish a state-of-the-art manufacturing operation. The Packaging Technician performs visual inspection and packaging activities in strict compliance with regulatory requirements, current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs).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 activities in accordance with cGMP, SOPs, and regulatory requirements.
  • Ensure packaging operations meet or exceed site safety, quality, and compliance metrics while following all site standards and policies.
  • Set up and operate packaging equipment, including labelers, cartoning equipment, and serialization stations.
  • Accurately document all activities within batch records, protocols, and other required documentation.
  • Support equipment validation and qualification activities for packaging operations.
  • Participate in training and assist with troubleshooting of packaging equipment and processes.
  • Assist Maintenance personnel with preventive maintenance and calibration activities related to packaging equipment.
  • Contribute to continuous improvement initiatives within the packaging area, including investigations and corrective and preventive actions (CAPA).
  • Follow all relevant Standard Operating Procedures (SOPs), work instructions, and site policies.
  • Maintain a high level of attention to detail to ensure product integrity and documentation accuracy.
  • Collaborate effectively with team members in a fast-paced, regulated manufacturing environment.

Essential Skills

  • At least 1 year of experience working in a pharmaceutical, production, or other regulated environment is preferred.
  • Previous experience in visual inspection, sterile packaging, clinical trial packaging, or related manufacturing activities is preferred.
  • Demonstrated ability to perform detailed visual inspections to identify product defects.
  • Good documentation skills, including accurate completion of batch records and protocols.
  • Strong attention to detail and commitment to quality and compliance.
  • Ability to work effectively in a team-oriented environment.
  • Good interpersonal skills and self-motivation.
  • Strong learning agility with the ability to quickly adapt to new processes and equipment.
  • Ability to work in a fast-paced, collaborative environment.
  • Excellent written and verbal communication skills.
  • Comfort working in a cGMP-regulated, cleanroom manufacturing setting.

Additional Skills & Qualifications

  • Experience with general production and packaging operations.
  • Familiarity with inspection of parts and components in a regulated environment.
  • Experience documenting activities in compliance with cGMP standards.
  • Background as a pharmacy technician or similar role in healthcare or pharmaceutical settings is beneficial.
  • Experience supporting equipment validation, qualification, and troubleshooting.
  • Exposure to continuous improvement initiatives, investigations, and CAPA activities.
  • Ability to follow detailed SOPs, work instructions, and site policies consistently.

Work EnvironmentThis role is based in a clean, state-of-the-art medical manufacturing facility in Nashville, TN that operates under FDA-regulated cGMP standards. The environment includes aseptic formulation and filling operations and a dedicated packaging area with equipment such as labelers, cartoning machines, and serialization stations. Team members work in a fast-paced, collaborative setting focused on safety, quality, and regulatory compliance. The position follows structured shifts: first shift runs Monday through Friday from 7:00 a.m. to 3:30 p.m., and second shift runs Monday through Friday from 3:00 p.m. to 11:30 p.m. The facility requires full cleanroom personal protective equipment (PPE), and team members must be comfortable with an in-depth gowning process appropriate for cleanroom operations. The site is undergoing significant capital investment and expansion, offering dynamic opportunities, rewarding career paths, and the chance to contribute to global health in a modern, growth-oriented manufacturing environment. Job Type & LocationThis is a Permanent position based out of Nashville, TN. Pay and BenefitsThe pay range for this position is $22.00 - $23.00/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) Job Type & LocationThis is a Permanent position based out of Nashville, TN. Application DeadlineThis position is anticipated to close on Nov 26, 2026. Workplace TypeThis is a fully onsite position in Nashville,TN.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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.

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