Actively Interviewing for Aseptic Technician to join pharmaceutical client in Bogart, GA! Job Description The Egg White Harvest Technician I performs daily egg white harvest operations in a pharmaceutical manufacturing environment, ensuring all activities comply with current Good Manufacturing Practices and established Standard Operating Procedures. This role conducts harvests, environmental monitoring, sampling, line clearances, and documentation while maintaining a clean, organized harvest suite, supplies, and equipment. The technician follows Good Documentation Practices, supports production by working assigned shifts, weekends, and holidays as needed, and consistently upholds individual and team safety standards. Responsibilities Perform egg white harvest activities according to established Standard Operating Procedures and current Good Manufacturing Practices. Execute Master Batch Records in compliance with Good Documentation Practices, ensuring accurate, complete, and timely recordkeeping. Perform aseptic manipulations within a laminar flow hood following established procedures to maintain product integrity. Prepare materials and equipment required for egg white harvest and related processes. Conduct environmental monitoring and process sampling to support quality and compliance requirements. Perform line clearances and verify that equipment and areas are properly prepared before and after operations. Maintain inventory control of materials, supplies, and equipment used in the harvest suite and related areas. Revise and update cGMP documentation as directed to reflect current processes and practices. Complete all cGMP documentation according to approved procedures and Good Documentation Practices. Support shipping and receiving activities related to materials and products as needed. Clean and sanitize equipment according to established procedures to ensure readiness for use. Maintain general housekeeping of the laboratory and harvest suite to support a safe and compliant work area. Follow individual and team safety policies and procedures and demonstrate accountability for safe work practices. Work shifts, weekends, and holidays as needed to support production schedules. Withstand exposure to -20°C environments as required for specific tasks. Collaborate effectively with colleagues and communicate clearly to support smooth operations and teamwork. Essential Skills High school diploma or equivalent. Excellent verbal and written communication skills. Ability to work independently and as part of a team in a manufacturing or laboratory setting. Ability to adapt to changing priorities and adjust work plans accordingly. Ability to read, write, and understand spoken English at an 8th grade level. Ability to wear an N-95 respirator, examination gloves, and other required personal protective equipment. Willingness to work hard and be open to learning new tasks and procedures. Ability to frequently lift and carry approximately 15 pounds unassisted and 30 pounds with assistance, with or without accommodation. Ability to stand, walk, and move for prolonged periods of time in a manufacturing environment. Ability to climb stairs or ladders as needed for facility access and tasks. Ability to gown and degown personal protective equipment and uniforms according to procedures. Ability to use a computer with a keyboard and mouse for documentation and communication. Ability to collaborate with others and maintain general availability during standard business hours. Additional Skills & Qualifications Biotech certificate, Associate's degree, or Bachelor's degree is preferred. Experience with inventory control methods and electronic inventory systems is preferred. Experience in a manufacturing environment is a plus. Prior exposure to GMP or laboratory environments is beneficial. Familiarity with aseptic techniques and working in laminar flow hoods is advantageous. Experience in roles such as lab technician, environmental monitoring, lab assistant, research assistant, or research associate is helpful. Ability to prioritize and organize work to ensure timely completion of assigned tasks. Work Environment This role operates in a pharmaceutical manufacturing environment that emphasizes safety, cleanliness, and regulatory compliance. The position follows a Sunday-Thursday or Tuesday-Saturday schedule from 8:00 a.m. to 4:30 p.m., with the expectation of supporting shifts, weekends, and holidays as needed. Work is performed in laboratory and production areas, including egg white harvest suites and laminar flow hoods, with regular use of computers and electronic systems for documentation and inventory control. The environment may require exposure to -20°C conditions for certain tasks. Team members frequently stand, walk, move, lift, and climb stairs or ladders during their shift. The role requires consistent use of personal protective equipment such as N-95 respirators, examination gloves, and other protective garments, including full gowning and degowning procedures. The culture emphasizes teamwork, adaptability, and continuous learning, with a strong focus on Good Manufacturing Practices, Good Documentation Practices, and maintaining a safe, well-organized work area. Job Type & Location This is a Contract position based out of Bogart, GA. Pay and Benefits The pay range for this position is $16.00 - $18.00/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) Workplace Type This is a fully onsite position in Bogart,GA.
Application Deadline This position is anticipated to close on Jun 12, 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 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.