Drug Product Manufacturing Associate I - Formulations 1st Shift

PCI TRGR Penn Pharmaceutical Services Ltd; San Diego (CA); On-site; USD 30,000 - 33,000; Full time

Benefits offered by this job

Health Insurance

401(k) Plan

Paid Time Off

Flexible Spending Account

Job summary

PCI Pharma Services is hiring a Drug Product Manufacturing Associate I - Formulations in San Diego, CA. The role supports routine production, aseptic operations, and cGMP compliance within the Drug Product group.

You will gain exposure to Master Batch Records, SOPs, and manufacturing equipment, while collaborating with the Drug Product team to ensure timely, compliant execution. The position requires a Life Sciences degree (or equivalent) and 0–2 years of related experience, with attention to

Qualifications

• High School Diploma required.
• 1st degree or higher in life sciences preferred.
• 0–2 years of experience in manufacturing or lab environment.
• Detail oriented with strong written and verbal communication.
• Familiarity with cGMP, manufacturing, machine operations, and data entry.
• Microsoft Office familiarity.

Responsibilities

• Performs various manufacturing tasks such as sterile filtration, formulation, in-process testing in accordance with SOPs and cGMP.
• Supports implementation of manufacturing procedures and production schedules.
• Assists other personnel with technical issues during the shift.
• Initiates revisions to Master Batch Records, SOPs, and department aids.
• Maintains production resources and assists with product development projects.
• Operates production equipment including TFF, Rotavap, Microfluidizer, and autoclave.

Skills

Attention to detail

Communication skills

Independent worker

Team player

Education

Bachelor’s degree in life sciences

High School Diploma

Tools

Microsoft Office

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary: 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.

Shift: 1st Shift Hours: 8AM - 5PM

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.

Qualifications

• High School Diploma required.
• Bachelor’s degree in a life sciences discipline or equivalent preferred.
• 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.

The hiring rate for this position is $21.69 - 24.41 plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan.

#LI-AC1 Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how.