Hiring: SDO_Quality Assurance Specialist Company: PCI Pharma Services Location: San Diego, CA Job Posted Time: 2026-09-16 13:51:57 Employment Type: Full-time Target Skills & Keywords : Microsoft Excel, Quality Assurance About the job Required Skills: •To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. •Independently perform product lot disposition by reviewing executed packaging records for completeness, accuracy, and compliance with cGMP requirements and company procedures with minimal supervision. •Own and execute document control activities within the electronic Quality Management System (eQMS), including document issuance, revision, approval workflows, reconciliation, archival, and retirement activities, ensuring compliance with GDP and document control procedures. •Coordinate, administer, and maintain the site training program, including assignment, tracking, and monitoring of GMP training curricula and periodic training requirements. •Oversee onboarding and training activities for new hires, ensuring timely completion of required GMP and On-the-Job Training (OJT) requirements. •Deliver and facilitate GMP and procedural training sessions as required to support employee competency and compliance. •Monitor training compliance metrics and proactively follow up on overdue training assignments to maintain inspection readinesss. •Collect, analyze, trend, and report document control and training quality metrics to support continuous improvement initiatives and management review activities. Qualifications: •The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. •University/college education in the fields of math, or science, or relevant practical experience •Knowledge and experience with manufacturing processes and products •Exceptional attention to detail and proofing ability •Sound judgement when approving or rejecting work in keeping with specifications and internal quality control standards •Effective interpersonal skills and the ability to influence and negotiate in the presentation of feedback to colleagues and superiors •Computer knowledge to use software programs such as Access, Word, Excel, Internet, and custom company software, (ERP) •Excellent organizational, and time management skills to ensure deadlines are met •Knowledge of GMP and pharmaceutical standards is an asset •Demonstrated capacity to demonstrate attention to detail. Compensation: •$70,304 - $75,928 / year •Competitive benefits and rewards package •The hiring rate for this position is $70,304-75,928 plus eligibility for an annual performance bonus Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!