Quality Assurance Associate – 2nd Shift, cGMP Focus

Tower-Laboratorie; Clinton (CT); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

401(k) with company match

Tuition assistance

Flexible Spending Accounts

Life and AD&D insurances

Safety shoe and glasses reimbursements

Job summary

Tower Laboratories, Centerbrook, CT, seeks a QA Auditor on 2nd shift to enforce the quality system and ensure product integrity. You will work with production to verify that effervescent tablets and powders meet specifications in a cGMP environment.

Responsibilities include audits, investigations, document reviews, and calibration verification. A foundation in regulated industries and strong attention to detail are essential for success.

Qualifications

• Minimum of 2 years’ experience in pharmaceutical, food/beverage, nutritional supplement or another highly regulated environment.
• Demonstrated strong attention to detail.
• Knowledge of cGMP regulations highly preferred.
• Working knowledge of MS Word and MS Excel.
• Must be able to read and follow directions, complete paperwork and communicate effectively in English.
• Excellent organizational skills.
• Good interpersonal skills; ability to communicate effectively with all levels of plant personnel.
• Strong team player, demonstrated team attitude and behaviors.

Responsibilities

• Perform product manufacturing audits throughout process and conduct in-process testing to ensure specifications.
• Conduct packaging audits to ensure final product meets packaging specs and is within AQL.
• Investigate root causes when products or processes deviate from specs.
• Assist in internal audits of cGMP to ensure compliance with procedures.
• Audit finished/ batch production documents before final release by QA Manager.
• Communicate manufacturing deficiencies to relevant personnel.
• Verify instrumentation calibration and perform calibrations as needed.
• Work collaboratively with all departments to meet company objectives.
• Adhere to Safety, cGMP and company procedures.

Skills

Attention to detail

English proficiency

Team player

MS Word

MS Excel

Education

High School Diploma or equivalent; degree desirable

Tools

cGMP knowledge

Job description

Tower Laboratories, Centerbrook, CT, seeks a QA Auditor on 2nd shift to enforce the quality system and ensure product integrity. You will work with production to verify that effervescent tablets and powders meet specifications in a cGMP environment.

Responsibilities include audits, investigations, document reviews, and calibration verification. A foundation in regulated industries and strong attention to detail are essential for success.