Lead Manufacturing Bulk Technician

Pacira Pharmaceuticals, Inc.•San Diego, CA

6d•$33 - $45

About The Position

At Pacira, innovation meets purpose. Pacira BioSciences, 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. Summary: This role leads daily activities and performs manufacturing tasks and operations at an advanced level for bulking and weigh and dispense operations required in the preparation and sterile production of liquid injectable, sustained-release pharmaceutical products under cGMP regulations and aseptic cleanroom conditions.

Requirements

5 years of industry experience in the pharmaceutical or closely related industry required
A high school diploma/GED is required
Organizational skills and an ability to perform assignments with a high degree of independence
The ability and willingness to work as a member of a team, good interpersonal skills
Ability to work with minimal direct supervision and be self-driven to meet the schedule
Must have good attention to detail, documentation skills, and the ability to follow written procedures in a GMP environment
Must possess strong written and verbal English communication skills
Must have strong organizational skills and the ability to multi-task
Must understand and be proficient with basic arithmetic calculations, including calculating elapsed time and ratio calculations
Computer proficiency, including knowledge of Microsoft Word, Outlook, and Excel applications, is required
Ability to accommodate production requirements that may occasionally require 50+ hour workweeks, including extended day hours and weekends
Ability to work a 12-hour shift (includes overtime eligibility)
Ability to work weekends

Responsibilities

Work directly with supervisor to coordinate daily activities for process and personnel.
Maintain scheduling timeline while adhering to GMP and SOP guidelines.
Identify and implement process improvements.
Transact materials in ESI to maintain accurate inventory levels
Perform routine inventory cycle counts
Maintain production areas and records - OEE spreadsheets, Manufacturing Tracker Spreadsheets and Shift Pass downs.
The required tasks and areas of assignment include: CIP, SIP, and solution prep, set-up and preparation of the area for bulk manufacturing, perform GMP area cleaning, utilize the automated control systems, and other routine tasks
Perform Weigh and Dispense Operations utilizing protocols and SOPs by weighing the required quantity for each material according to the Manufacturing Batch Record (MBR).
Use computer system and weighing balance equipment.
Understand critical process parameters and steps of activities sufficiently to act as a trainer for new employees.
Complete GMP documentation (Batch Records, Forms, Charts, Data Entry).
Read, comprehend, and adhere to standard operating procedures (SOPs).
Participate in the development and production of pipeline products.
Author or assist in drafting and revising departmental procedures and practices.
Identify and communicate floor observations to supervisory staff.
Maintaine a high level of proficiency with process equipment and automated control systems with the ability to troubleshoot, escalate issues, and determine corrections.
Provide guidance to less experienced operators on gowning, interventions, and aseptic manipulations, and maintain aseptic gown qualifications and APS participation.
Assist in maintaining the production areas and records in a cGMP state.
Adhere to all EH&S policies, procedures, and guidelines.