QA Associate : Lot Release & Disposition

Overview

At Pacira, innovation meets purpose.

Pacira Bio Sciences, Inc. is a pioneer in non-opioid pain management and regenerative health solutions. Today, we're building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskeletal pain. Our culture is built on collaboration, innovation, and a shared commitment to helping patients recover faster. We are redefining what's possible in pain management-and we can't do it without talented people like you.

Why Join Us?

At Pacira, every career is more than a job. Our mission drives us, and every day, we challenge ourselves to achieve the extraordinary. Integrity is at the core of who we are. We value diverse perspectives and the collective strength of a unified team. Join the team in making better possible for patients everywhere.

Purpose:

This person provides hands on quality assurance support to manufacturing operations with a primary focus on batch record review and lot release activities. This role supports the organization's commitment to GMP compliance by monitoring manufacturing activities, reviewing executed batch documentation, and ensuring conformance to established quality systems, procedures, and regulatory requirements. The QA I Associate works closely with cross-functional teams to identify and address quality risks while maintaining real-time floor presence to support compliant operations.

Responsibilities
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Supervisory Responsibilities:

This person has no direct supervisor responsibilities.

Interaction

Continuously interacts with other members of the Manufacturing, Quality Control, Supply Operations, Microbiology and Product teams.

Education and Experience:

• 1 year of industry experience in the pharmaceutical or a closely related industry preferred
• BS/BA degree in scientific discipline desirable

Qualifications:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

This job requires weekend, holiday and off shift work hours.

Knowledge, Skills, and Abilities
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Work Environment:

Typical office setting, cubicles, noise level is moderate with consistent printer, telephone ringing and conversation. The work environment also includes warehouse and manufacturing areas.

Physical Demands:

While performing the duties of this job, the employee is regularly required to sit, move between spaces, and reach

with hands and arms. Close vision and the need to focus on computer screen, use of hands, fingers, and wrist to type

on keyboard and manipulate mouse. Will need to lift and move items weighing up to 30 pounds.

Employee is required to work in a cleanroom environment, which requires gowning consisting of coverall, foot and

head coverings, facemask, and gloves. Noise level is moderate with consistent equipment operation. This position requires the individual to pass the AQL particle inspection test of in process product vials.

Benefits:

• Medical, Prescription, Dental, Vision Coverage
• Flexible Spending Account & Health Savings Account with Company match
• Employee Assistance Program
• Mental Health Resources
• Disability Coverage
• Life insurance
• Critical Illness and Accident Insurance
• Legal and Identity Theft Protection
• Pet Insurance
• Fertility and Maternity Assistance
• 401(k) with company match
• Flexible Time Off (FTO) and 11 paid holidays
• Paid Parental Leave

The base pay range for this role is $23.00 per hour. to $30.00 per hour. This role is…