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!
The purpose of this position is to assist with laboratory functions which may include washing glassware, stocking glassware and lab supplies, and/or perform laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products.
Essential Duties &
Receiving and labeling of incoming Finished Product samples
Back-up for receiving and labeling of incoming Stability and Special Studies samples
Perform sample disposal after testing and review is completed
Collecting and washing glassware and replenish cleaned glassware in QC Labs
Perform qualification and feasibility tests of materials used for testing
Shipping of samples and/ or supplies to contract labs
Management of QC logbooks, to include requesting and tracking
Understand and comply with accepted laboratory and safety procedures, including Good Manufacturing Practices
Responsible for transfer of QC Data Packets to QA DC by performing the following tasks:
Organizing QC data packets (Finished products, Stability, Raw Material-Patheon) for scanning
Coordinate scanning and archiving of QC data packets with QA DC
Update/maintain inventory tracker for transferred QC data packets
Support the QC team as needed for the test and release of finished product for US Commercial and Clinical use
Support the QC team as needed for the test and release of finished product for EU Commercial and Clinical use prior to final QP Certification of batches for EU distribution
Support the QC team as needed for the test and release of raw materials for US and EU Commercial and Clinical use
This position works closely with other Operation Groups (QA, Manufacturing, Materials, and Microbiology) and Research Development groups.
Education and Experience:
~1 year of experience in a laboratory environment, preferably in a pharmaceutical or biotech operation.
High school diploma or equivalent
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.
Knowledge, Skills, and
Demonstrated computer proficiency (e.g., word processing, spreadsheets, graphing, etc.)
Ability to follow analytical procedures and protocols
Good laboratory techniques
Ability to work in a methodical and organized fashion
Ability to write in a concise, logical fashion
Ability to manage multiple responsibilities with a high degree of self-motivation
Good oral, written, and interpersonal English communication skills