Filling Technician I

Job Description

Job Description

Job Title: Filling Technician I
Job Description

This entry-level Filling Technician I position supports a finished product pharmaceutical facility by operating and monitoring a brand-new manufacturing line for high-demand pharmaceutical products. You will work in a fast-paced manufacturing environment, loading materials, completing fully electronic documentation, and performing process checks to ensure product quality and compliance. This role suits motivated individuals who want to build a career in pharmaceutical manufacturing, enjoy hands-on work, and bring a tech-savvy, process-improvement mindset to a highly regulated setting.

Responsibilities

• Operate and support a new pharmaceutical manufacturing line to meet production targets and quality standards.
• Load materials accurately into equipment and systems according to established procedures and batch requirements.
• Complete electronic batch records for all processes, ensuring accuracy, completeness, and compliance with Good Manufacturing Practices (GMP).
• Maintain detailed and accurate log book entries and document work orders to support traceability and regulatory requirements.
• Perform in-process checks and process verifications to ensure product quality and adherence to standard operating procedures.
• Prepare and maintain Batch Packaging Records (BPR) for all materials loaded and products produced.
• Identify recurring issues on the line, report them promptly, and actively contribute to developing and implementing practical solutions.
• Communicate clearly and professionally with team members and cross-functional partners to coordinate activities and resolve issues.
• Apply a critical-thinking approach to daily tasks, identifying opportunities to improve processes, efficiency, and quality.
• Use electronic systems and tools for documentation, data entry, and process monitoring, ensuring accurate and timely updates.
• Follow GMP, aseptic techniques, and safety procedures at all times to maintain a compliant and safe manufacturing environment.
• Participate in training and continuous learning to build knowledge in pharmaceutical manufacturing, biotechnology, and process operations.
• Support a culture of continuous improvement by sharing ideas, providing feedback, and engaging in problem-solving discussions.

• Previous manufacturing experience in a GMP environment.
• Aseptic experience in a regulated or controlled production setting.
• Exposure to and understanding of Good Manufacturing Practices (GMP).
• Demonstrated interest in working in pharmaceutical manufacturing.
• Ability to work effectively in a manufacturing environment and remain on your feet for extended periods.
• Strong communication skills, with the ability to clearly convey information and collaborate with team members.
• Critical-thinking skills and a process-improvement mindset, with the ability to identify issues and propose solutions.
• Technical savvy and comfort working with fully electronic documentation systems and digital tools.
• Motivation to learn and build a career in pharma, even if coming from non-manufacturing backgrounds such as childcare, automotive, or office environments.

• Bioworks certification or completion of a BioWorks program.
• Associate degree in Biotechnology or related field, demonstrating strong desire to be in pharma and initiative to learn more.
• Manufacturing environment experience, particularly understanding what it is like to work on your feet for 12-hour shifts.
• Cleanroom experience in a controlled or classified environment.
• Gowning experience, including proper donning and doffing of cleanroom garments.
• Two years of aseptic experience in a GMP or similar regulated environment.
• Additional GMP experience beyond the minimum requirements.

This role is based in a finished product pharmaceutical manufacturing facility operating on a night shift schedule. You will work in a production environment that may include cleanroom areas and aseptic processing spaces, where adherence to GMP, safety procedures, and gowning requirements is critical. The position involves being on your feet for up to 12 hours, working with automated equipment, electronic documentation systems, and digital tools to manage batch records and process data. The facility focuses on producing life-saving products for individuals with conditions such as diabetes and chronic weight-related needs, and emphasizes a strong, inclusive company culture that supports diversity, inclusion, and work-life balance. Team members are encouraged to perform at a high level and are given opportunities to grow their careers in various directions within the organization.

Job Type & Location

This is a Contract position based out of Clayton, NC.

The pay range for this position is $23.50 - $23.50/hr.

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)

This is a fully onsite position in Clayton,NC.

This position is anticipated to close on Jun 3, 2026.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 View email address on jobswipe.net 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.