About Pacira

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients.

Each of our 3 marketed products, both in pharmaceutical and medical device, represent cutting edge technologies for pain management.

We have 700+ employees and have averaged double digit growth year over year for the past 5 years, with $500M in revenue. We are small enough for you to make your mark, and big enough for you to learn and grow!

We have facilities in New Jersey, California and Florida. Our San Diego, CA campus is a world class manufacturing and R&D facility. We are rapidly growing and have opportunities across all of our sites and functional areas.

Why work with us?
Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people. At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking – a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let’s pursue excellence together.

Summary:

This position supports the development, implementation and maintenance of the GMP training program and activities at the Science Center Campus and Headquarters.

Essential Duties & Responsibilities:

• Provide exceptional customer service to Pacira’s internal and external customers in all assigned tasks.
• File and maintain personnel records for GMP training and job-specific documentation in both electronic and hard copy formats.
• Manage the training calendar, coordinate training logistics, compile and deliver training materials.
• Administer and support the ComplianceWire Learning Management System to include training new system users.
• Publish training reports and metrics.
• Support regulatory inspections and partner audits.
• Other duties as assigned.

Supervisory Responsibilities:

This role has no direct supervisory responsibilities.

Education and Experience:

• Entry-level position. Prior pharmaceutical industry experience in Quality Assurance, Training, or related function preferred, but is not required.
• AA/AS degree or equivalent experience in a clerical or training function.

Knowledge, Skills, and Abilities:

• Must have an excellent customer-service orientation and a strong attention to detail.
• Ability to manage multiple responsibilities to complete assignments within established timelines.
• Strong communication, interpersonal, and organizational skills.
• Proficiency in Microsoft Excel, Outlook, and Word applications.
• Prior experience with ComplianceWire and/or MasterControl desirable.
• Flexibility to work varying schedules to support occasional weekend, holiday and off shift work hours.

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:

May regularly sit, talk, move between spaces, reach with hands and arms and stoop. Regularly focus on a computer screen and use hands, fingers and wrists to type on keyboard and manipulate mouse. Commonly lift and move boxes of paper and binders weighing up to 20 pounds.

The base pay range for this role in California is $26.15 per hour to $35.96 per hour. This role is classified as non-exempt and eligible for over-time.

The range is what we reasonably expect to pay for this role. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications.