QS - Line Auditor

Job Description

Job Title: QS Associate I & II – Line Auditor

Location: Lakewood, NJ 08701

Hours: Monday-Friday, 7:00AM-4:00PM

Join Our Team:

At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetics, over-the-counter and medical devices across skincare, haircare, oral care, and healthcare products.

But beyond that, we make a difference. We make a difference in the lives of our people, we make a difference in the community around us, we make a difference in the health of our planet for a better, brighter, more beautiful future for all.

We value quality-focused professionals who take pride in maintaining high standards of compliance and documentation. As a QS Associate – Line Auditor, you’ll play a vital role in ensuring our manufacturing and packaging operations meet cGMP standards, internal procedures, and customer specifications. From reviewing batch records and managing quality documentation to supporting investigations and performing in-process inspections, you'll help ensure our products are safe, compliant, and ready for market.

What We Offer:

Competitive Pay

Pay Range: $17.30/hr - $21.63/hr

Bonus: Exempt employees are eligible for a bonus in accordance with Accupac’s Bonus Plan.

o The posted job may span more than one career level. The final offer, including level and pay, will be determined based on a variety of factors such as the candidate’s relevant job and industry experience, education, knowledge, skills, geographic location, and abilities. Internal equity and alignment with market data will also be considered. We are committed to providing fair and competitive compensation based on each candidate’s qualifications and fit for the role.

Employees are eligible for the following benefits:

o Medical, Dental, and Vision insurance

o Health Savings Account

o Life Insurance with Optional Supplemental Plan

o Pet Insurance

o Short-Term Paid Disability

o 401(k) Retirement Plan with Vested Company Match Contribution

o Paid Time Off (PTO)

o 10 Paid Holidays

o Health Advocacy Programs

· Career Growth

What You’ll Do:

Ensure compliance with cGMP standards, SOPs, and customer specifications across manufacturing and packaging operations

Manage the Annual Drug Product Review (ADPR) process

Support and manage Change Control activities from initiation through closure

Participate in and conduct investigations, including laboratory investigations

Initiate, track, and close CAPAs and perform effectiveness checks

Perform production line inspections and daily calibration checks

Conduct inspections and approvals of raw materials, components, and packaging materials

Review and approve manufacturing and packaging batch records for product release

Maintain accurate documentation and ensure adherence to Good Documentation Practices

File, archive, and update paper and electronic records

Perform sampling, testing, and reconciliation in accordance with approved procedures

Collaborate with cross-functional teams to resolve discrepancies and drive quality improvements

What We’re Looking For:

Bachelor’s degree required

QA Associate I: 0–2 years of Quality Assurance or Quality Control experience in a cGMP-regulated environment

QA Associate II: 2+ years of Quality Assurance or Quality Control experience in a cGMP-regulated environment

Experience with LIMS systems preferred

Strong attention to detail, organizational, and documentation skills

Familiarity with industry tools such as balances, torque meters, vacuum/seal strength testers

Proficient in Microsoft Office (Word, Excel, etc.)

Effective communication skills and ability to work independently and in teams

Ability to lift up to 40 lbs., stand for extended periods, and perform inspections requiring bending, color recognition, and peripheral vision

Ready to Apply?

Full-time