QA Associate - Temporary, Part-Time bei Tower Laboratories

Tower Laboratories is a leading effervescent product manufacturer in the U.S. We develop and manufacture over-the-counter medications, prescription pharmaceuticals, nutritional supplements, soft drink tablets and other consumer products on a contract basis. We are continually expanding our effervescent product base and currently have several new and interesting products in the research and development phase right now. We are a family owned company and have been in business for over 40 years. www.towerlabs.com.
 
POSITION SUMMARY:

This is a Temporary position September through December 31, 2025. Part time, 20 hours per week, preferably in afternoon/early evening. Clinton, CT facility.

Work closely with production and QA staff to ensure that our effervescent tablets and powders are manufactured in accordance with applicable procedures, specifications and in a cGMP (current Good Manufacturing Practices) compliant manner. Partners with manufacturing throughout production life cycle to assure that procedures are followed and activities are appropriately documented.   

ESSENTIAL FUNCTIONS:

• Conduct various packaging audits by pulling samples from production or warehouse and inspecting to ensure it meets pre-determined specifications and is within the allowed accepted quality limits (AQL); 
• inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications.
• Perform product manufacturing audits throughout process through observation and by conducting in-process testing to ensure product meets specifications.  
• Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications.
• Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies.
• Audit finished/completed batch production documents for procedural or mathematical errors prior to final review and release of product by the QA Manager.
• Communicate identified manufacturing deficiencies to key personnel (Machine Operator, Quality Supervisor/Manager, Production Manager, etc.).  
• Work as a team member; be cooperative with all departments and staff to meet company objectives.
• Perform all work in accordance with established Safety, cGMP and company procedures.
• Other responsibilities as assigned.

ESSENTIAL SKILLS AND EXPERIENCE:

• Minimum of 2 years’ experience in either 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.

PHYSICAL DEMANDS:

• Lift, push, pull up to 25lbs. on occasional basis
• Climb stairs, walking throughout manufacturing/warehouse areas
• Must be able to wear safety shoes & safety glasses when in manufacturing/warehouse areas

EDUCATION:  

High school diploma or equivalent; degree desirable.

This medium sized family business is headquartered in the scenic town of Centerbrook in Southeastern Conn., and offers a clean, humidity & temperature controlled, friendly working environment and complete benefit package for full time, regular positions. 

Qualified candidates apply today to start the conversation! Tower Labs is a Socially Responsible Employer and a great place to work!