Quality Control Technician

Akina Pharmacy•Sterling, VA

1d•Onsite

About The Position

The Quality Control Technician plays a critical role at Akina Pharmacy, ensuring that compounded sterile medications are meticulously inspected to ensure the highest quality standards. This position requires great attention to detail, a strong sense of accountability, and the ability to thrive in a fast-paced, goal-oriented environment. As a Quality Control Technician, you will manage one of the final stages of the sterile compounding process by visually inspecting each finished sterile compound product to ensure that each released product stays within the quality and compliance standards. In addition to visual inspections, you will assist with environmental monitoring of the labs, and any other tasks assigned by the Quality Assurance and Quality Control Manager. Success in this role is driven by a commitment to Akina Pharmacy’s core values of Excellence Always, Go-Getter’s Unite, Compassion For All, and Called To Serve. If you are highly organized, detail-oriented, and enjoy contributing to a team dedicated to improving patient care, this position offers a rewarding opportunity to make a meaningful impact. You will love it here if you are motivated by Akina’s Core Identity Values: Excellence Always, Go-Getter’s Unite, Compassion For All, Called To Serve. You’ll have success here if you value clear processes and get, want, and have capacity to do the following things: Finished Product Inspection and Testing: Perform visual inspections of finished products to identify defects, particulate matter, or other deviations from specifications. In-Process Quality Checks: Monitor and verify in-process production activities to ensure compliance with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP). Collect and analyze data during compounding, filling, or packaging to identify trends or deviations. Environmental Monitoring: Perform viable and nonviable particle sampling and readings in classified environments to ensure compliance with USP <795>/<797>/<800> or other relevant guidelines. Document and report environmental trends to proactively address risks to product sterility. Personnel Monitoring and Sampling: Conduct gloved fingertip sampling to evaluate aseptic technique and ensure operator compliance with sterility requirements. Report findings and assist in identifying corrective actions or retraining needs for personnel. Documentation and Reporting: Accurately document all inspection and testing results in compliance with USP, FDA and regulatory guidance. Collaborate with QA to ensure timely reporting of non-conformances, CAPA investigations, and release decisions. We train our team to help them succeed, and everyone on our team helps with our success. In this role, you’ll be accountable for hitting the following numbers: Conduct manual visual inspection process and qualify units as per visual inspection process on compounded sterile medications (CSPs) (Up to 2000 vials per day) Perform acceptable quality limit inspections on compounded medications (Up to 10 batches per day) Analyze viable air and surface samples (both solid and liquid media) for growth, turbidity and particulate matter (up to 10 batches per day) Our company runs on EOS purely. That means as a member of this team, you will have a leader who: Gives clear directions and expectations Makes sure you have the necessary tools Delegates appropriately Has effective meetings Meets one-on-one with you quarterly or more, if needed Rewards and recognizes your performance

Requirements

High school diploma or GED with work experience.
Commitment to maintaining continuing education and staying updated on industry regulations and best practices.
1-2 years of experience in a quality or manufacturing department with a focus on accuracy, efficiency, and compliance (preferred, not required).
Proven ability to prioritize tasks, manage time effectively, and maintain productivity benchmarks in a fast-paced environment.
Strong written and verbal communication skills, with the ability to interact effectively with pharmacists, patients, and other team members.
Collaborative mindset to ensure alignment with pharmacy operations and patient care goals.
Proficiency in pharmacy management systems and software for prescription entry, inventory tracking, and workflow management.
Ability to learn and troubleshoot dispensing equipment and technology as needed.

Nice To Haves

Familiarity with 503A or 503B compounding pharmacies, including knowledge of aseptic techniques, hazardous drug handling, or specialty medication quality control/assurance (preferred, not required).

Responsibilities

Perform visual inspections of finished products to identify defects, particulate matter, or other deviations from specifications.
Monitor and verify in-process production activities to ensure compliance with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
Collect and analyze data during compounding, filling, or packaging to identify trends or deviations.
Perform viable and nonviable particle sampling and readings in classified environments to ensure compliance with USP <795>/<797>/<800> or other relevant guidelines.
Document and report environmental trends to proactively address risks to product sterility.
Conduct gloved fingertip sampling to evaluate aseptic technique and ensure operator compliance with sterility requirements.
Report findings and assist in identifying corrective actions or retraining needs for personnel.
Accurately document all inspection and testing results in compliance with USP, FDA and regulatory guidance.
Collaborate with QA to ensure timely reporting of non-conformances, CAPA investigations, and release decisions.
Conduct manual visual inspection process and qualify units as per visual inspection process on compounded sterile medications (CSPs) (Up to 2000 vials per day).
Perform acceptable quality limit inspections on compounded medications (Up to 10 batches per day).
Analyze viable air and surface samples (both solid and liquid media) for growth, turbidity and particulate matter (up to 10 batches per day).