Quality Technician

The Quality Technician is responsible for performing hourly inspections and providing support to ensure compliance with current Good Manufacturing Practice (cGMP) and internal procedures. The successful candidate will ensure overall compliance, including testing and methods in accordance with cGMP, and will inspect incoming components, in-process products, and finished products as per documented specifications.

Responsibilities

• Assist with the inspection of incoming components according to documented specifications.
• Assist with the generation and approval of controlled labels using provided programs.
• Record data and maintain accurate records in accordance with cGMP documentation practices for accuracy and completeness.
• Retrieve documents using the EQMS computer system.
• Troubleshoot quality concerns that may arise during the inspection of incoming components and report to the Quality Manager.
• Verify the calibration of all inspection test equipment and maintain accurate records.
• Perform data entry and retrieval using the computer system.
• Work overtime, weekends, or alternate shifts as needed.
• Assist in the generation and resolution of corrective and preventive action plans (CAPAs).
• Assist in the documentation and resolution of nonconforming material reports and process discrepancy reports.
• Ensure nonconformances are initiated and reported promptly.
• Maintain work area orderliness and cleanliness.
• Ensure test equipment is maintained and records are kept.
• Ensure equipment is calibrated before use.
• Communicate issues and procedures among multiple departments effectively.
• Interact professionally with co-workers.

• Knowledge of Current Good Manufacturing Practice (cGMP) Regulations for medical devices and pharmaceuticals.
• Ability to manage daily activities to support business operations.
• Ensure timely completion of paperwork in compliance with cGMP.
• Determine root cause and develop corrective and preventive action plans for investigations, CAPA, and OOS issues.
• Maintain operational efficiency and compliance with all test equipment and processes.
• Provide necessary QA support for rapid commercialization of new products and processes.
• Perform or assist in required cGMP validations.
• Review in-process batch records and equipment notebooks daily.
• Proficiency in Microsoft Excel, Word, and PowerPoint.
• Serve as a backup for other QA Technicians as needed.
• Excellent written and verbal communication skills for interdepartmental communication.

• Good writing skills.
• Energetic and detail-oriented.
• Flexible and self-starter.
• Ability to work well with others and under pressure.
• Ability to work with minimal supervision and manage multiple priorities.
• Trustworthy and dependable.
• Computer literate.
• High School Degree with 3+ years of experience in the pharmaceutical industry.
• Associate’s degree preferred but not required.
• Prior Quality Technician experience preferred.

This position involves working in a Liquid & Topical Manufacturing and Packaging environment. Full manufacturing and lab services include bottling, tubes, vials, pouching, form-fill-seal, kit assembly, and secondary packaging, within facilities totaling 184,000 square feet. The role requires physical activities such as climbing, walking, stooping, kneeling, and lifting up to 35 lbs. Employees may be exposed to inside and outside environmental conditions, including dust and chemicals, and warehousing environments. The work environment may include loud noise levels and requires appropriate attire to ensure safety and compliance.

Job Type & Location

This is a Contract to Hire position based out of EASTON, MD.

Pay and Benefits

The pay range for this position is $18.00 - $21.00/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 EASTON,MD.

Application Deadline

This position is anticipated to close on Nov 21, 2025.

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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.