Quality Assurance Technician

Socket.dev; Southlake (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Healthcare coverage

401(k) match

Paid Time Off

Life Insurance

Job summary

Evexias is seeking a Quality Assurance Technician to provide on-the-floor support during receiving, manufacturing, and packaging of implantable hormone pellets. You will perform inspections, line clearances, and in-process verifications, documenting observations and escalating issues to maintain compliance.

The role ensures proper material handling, adherence to procedures, and real-time quality oversight across QA activities, fostering a compliant manufacturing environment.

Qualifications

• High school diploma or equivalent required.
• At least 2 years of experience in quality, inspection, manufacturing, or a regulated environment.
• Ability to read and follow written procedures, specifications, and batch records.
• Strong attention to detail with proficiency in Microsoft Office.
• Ability to complete all required cGMP, data integrity, and safety training.
• Preferred: Associate degree or experience in pharmaceutical manufacturing or 503B facilities.

Responsibilities

• Support cGMP manufacturing of implantable hormone pellets on the floor.
• Perform incoming inspections, line clearances, and in-process verifications.
• Document observations and escalate nonconformances to ensure compliant materials and processes.

Skills

Attention to detail

Reading procedures

Documentation literacy

Quality mindset

Data integrity awareness

Education

High school diploma or equivalent

Associate degree (pharma/manufacturing preferred)

Tools

Microsoft Office

Job description

Job Title:Quality Assurance Technician

Reports to:QA Specialist, Process Quality Excellence

Hours:8:30 AM - 5:00 PM

FLSA Status:Exempt

Full Time or Part Time:Full-Time

Choice isn’t optional. It’s everything.

In life. In health. In how we fight for our future. But somewhere along the way, medicine forgot that. Today’s system runs on one-size-fits-all answers and a cold “just take this” mentality. It’s efficient. It’s easy. It’s wrong.

EVEXIAS exists to blow that model wide open.

We’re pioneering a new way of doing things, and it starts by handing the decision back to the people who matter... you and your provider. TOGETHER, you choose treatments tailored to your whole self: mind, body, and spirit—including advanced, personalized hormone therapies designed to restore balance and vitality.

We go beyond surface symptoms to uncover the root cause, using today’s breakthroughs to ignite a transition of modern medicine…where insight runs deeper, care is pro‑active, and connection is everything. We dig deeper. Treat smarter. And restore something even more powerful than health—your Freedom. This isn’t just healthcare. It’s your comeback story, and that story starts with a choice.

Get Well. Live Well.

Position Summary

The Quality Assurance Technician provides on-the-floor support for the cGMP production of implantable hormone pellets. This role acts as a Quality presence during receiving, manufacturing, and packaging by performing incoming inspections, line clearances, and in-process verifications. The technician documents observations, identifies discrepancies, and escalates concerns to ensure only compliant materials and processes are utilized.

Incoming Material and Component Inspection

• Verify that active pharmaceutical ingredients, excipients, and packaging materials are received into appropriate status.
• Perform visual inspections for damage, cleanliness, and container-closure integrity.
• Compare items against purchase orders, packing slips, and specifications including lot numbers and expiration dates.
• Verify labeling, Certificates of Analysis, and Safety Data Sheets.
• Maintain material status labels and ensure inventory records reflect current disposition.
• Coordinate with Supply Chain, QC, and Warehouse for sampling, testing, or returns.

In-Process QA Oversight and Line Clearance

• Perform and document line clearance before start-up, after changeovers, and at operation completion.
• Verify room and equipment readiness, including cleaning status and calibration records.
• Conduct independent checks on material identity, quantities, equipment settings, and yield data.
• Provide floor oversight during weighing, pellet compression, and packaging operations.
• Review documentation in real-time for compliance with Good Documentation Practices.
• Ensure proper identification and segregation of all product, components, and waste.

Quality Documentation and Support

• Complete checklists, logs, and electronic records accurately and contemporaneously.
• Initiate or assist with quality event and nonconformance documentation.
• Maintain records in an audit-ready condition for regulatory or customer inspections.
• Communicate recurring errors or process signals to Quality management.
• Collaborate across departments while maintaining independent quality judgment.

Qualifications

• High school diploma or equivalent.
• At least two years of experience in quality, inspection, manufacturing, or a regulated environment.
• Ability to read and follow written procedures, specifications, and batch records.
• Strong attention to detail with proficiency in Microsoft Office.
• Ability to complete all required cGMP, data integrity, and safety training.
• Preferred: Associate degree or experience in pharmaceutical manufacturing or 503B facilities.

We are committed to supporting our team's health, financial future, and work-life balance. Our benefits include:

• Healthcare Coverage: Comprehensive health, dental, and vision insurance plans with company-subsidized premiums.
• Peace of Mind: 100% company-paid Short-Term Disability (STD), Long-Term Disability (LTD), and Life Insurance.
• Retirement Savings: A 401(k) plan featuring a 4% company match to help you build for the future.
• Work-Life Balance: Generous Paid Time Off (PTO) so you can relax, recharge, and take care of what matters most.

Our Mission

To empower individuals and providers with personalized, root-cause-focused care that restores health, balance, and freedom.

Our Vision

To lead a transformative shift in modern medicine…where deeper insights, proactive care, and personal choice define the future of wellness.

Our Values

• Care: We provide a welcoming, nurturing environment for our staff and our clients.
• Growth: We are dedicated to fostering beneficial change for ourselves and those we serve.
• Respect: We are unwavering in our commitment to speak with honor and listen without judgement.
• Partnership: Working collaboratively to build trust, value diverse perspectives, and achieve shared goals.
• Integrity: Acts with honesty, accountability, and alignment to company values

Your career in pharmaceutical innovation starts here!

The Fine Print:

FARMAKEIO Equal Employment Opportunity (EEO) Statement

FARMAKEIO is an equal opportunity employer committed to fostering an inclusive and diverse workplace. We comply with all applicable federal, state, and local fair employment laws, ensuring equal employment opportunities for all employees and applicants.Employment decisions at Evexias are based on qualifications, merit, and business needs. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, age, national origin, disability, genetic information, marital or familial status, military or veteran status, citizenship status, creed, domestic violence victim status, caregiver status, or any other characteristic protected under applicable laws.

This policy applies to all aspects of employment, including recruitment, hiring, training, compensation, benefits, promotions, transfers, terminations, and other terms and conditions of employment.

FARMAKEIO is dedicated to maintaining a workplace free from discrimination, harassment, and retaliation, ensuring a respectful and inclusive environment where all employees can thrive.

If you require a reasonable accommodation during the application process or in your role due to a disability or any other protected status, please contact [e-mail] for assistance.

Texting Privacy Policy and Information:

Message type: Informational; you will receive text messages regarding your application and potentially regarding interview scheduling. No mobile information will be shared with third parties/affiliates for marketing/promotional purposes. Message frequency will vary depending on the application process. Msg & data rates may apply. OPT out at any time by texting "Stop".