Drug Product Manufacturing Associate I - Formulations 2nd Shift

PCI Pharma Services•San Diego, CA

9d•$22 - $24•Onsite

About The Position

The Drug Product Manufacturing Associate I - Formulations is responsible for the implementation of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Associate I will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Associate I will develop a strong understanding of both the technical aspects of the role as well as the quality systems that govern cGMP manufacturing.

Requirements

High School Diploma required.
Minimum of zero to two (0-2) years of relevant experience in a manufacturing or laboratory environment.
Detail oriented with strong written and verbal communication skills.
Ability to work independently, within prescribed guidelines, or as a team member.
Demonstrated ability to follow detailed directions in a manufacturing GMP environment.
Familiarity with cGMP, manufacturing, machine operations, and data entry.
Must be familiar with Microsoft Office applications.

Nice To Haves

Bachelor’s degree in a life sciences discipline or equivalent preferred.

Responsibilities

Performs various manufacturing tasks, including sterile filtration, formulation, in-process testing, preparation of formulation components, and product development projects, in accordance with established Standard Operations Procedures (SOPs) and cGMP regulations.
Supports the implementation of manufacturing procedures and production schedules.
Effectively assists other personnel with technical issues and problems that may arise during the shift.
Initiates revisions to current Master Batch Records, SOPs, and department desktop aids.
Supports the maintenance of group production resources and assists with product development projects.
Expected to operate production equipment, including the TFF system, Rotavap, Microfluidizer, Homogenizer, chiller, rotary lobe pump, high shear mixer, SIP, autoclave, depyrogenation oven, and CIP system.
Maintains qualification to execute aseptic operations in GMP production facilities comprised of Grade A, B, C, and D manufacturing clean room areas.
Supports routine maintenance and troubleshooting of production equipment.
Accurately documents, completes, and reviews batch records, as needed.
Coordinates and leads preparation of materials and components for sterilization in autoclave or dehydrogenation oven.
Collaborates with other technical personnel on troubleshooting and engineering activities.
Collects and disposes of lab waste according to established Safety, Health, and Environment (SHE) procedures.
Maintains cGMP environment according to the production needs of the Drug Product group.
May be required to interact and collaborate with clients and third-party vendors.
Works closely with Production Planner to manage QAD work orders and ensure production materials are obtained according to the manufacturing schedule.
Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture.
Foster a safe and environmentally sustainable workplace by following all PCI EHS policies and procedures