QA Associate I: cGMP Documentation & On-the-Floor QA
$21.69 - $24.41 per hourPCI Pharma Services
The QA Associate I at PCI Pharma Services in San Diego is responsible for compliance with Quality Assurance requirements and collaborative team efforts. Duties include cGMP documentation review, area line clearance operations, and providing QA oversight during manufacturing. Ideal candidates should have a background in Life Sciences, with 0-2 years of QA or documentation experience. The role offers $21.69–$24.41 per hour and a competitive benefits package. #J-18808-Ljbffr PCI Pharma Services
$29.65 - $33.36 per hour
...routine and semi-routine QA Raw Materials... ...training programs, and documentation review for GMP operations... ...role promotes a compliant cGMP environment by following... ...production batch records and associated data for product... ...documentation, QA on the floor, manufacturing, or equivalent...FloorFull timeWork at officeFlexible hours- ...while ensuring compliance with cGMP regulations, internal... ...shift. Perform Quality on the Floor (QOTF) activities to ensure compliance... ...manufacturing activities and documentation. Support batch record review... ..., logbooks, forms, and associated documentation as authorized....FloorShift workNight shift
$70.3k - $75.93k
...inspection, product or material release, document control, production monitoring, tracking... ...labeling and packaging activities on the floor. Perform QC inspection or release of incoming... ...experience in Quality Assurance within a cGMP-regulated environment. Knowledge of Six...FloorFull timeFlexible hours$50 - $75 per hour
...initiatives, the team is seeking an experienced QA/QC Documentation Specialist to support GMP laboratory... ...protocols, testing protocols, and associated QC records Support documentation... ...archival activities Ensure compliance with cGMP, GDP, ALCOA+, and data integrity requirements...SuggestedHourly payContract work$24 - $45.5 per hour
...seeking a detail-oriented Quality Assurance (QA) Specialist to support operations in a... ...records, laboratory results, and quality documentation to ensure GMP compliance Support batch... ...Provide QA oversight on the manufacturing floor: Line clearance In-process checks Partner...FloorContract workTemporary work- ...protocols and work plans. May be assisted by QA Specialists and Sr. Specialists. Comply... ...production • Assist with packaging floor activities for primary and secondary (... ...production batch records, logbooks and other associated documents • Performs Quality verification of...FloorContract workImmediate start
$21.69 - $24.41 per hour
...future of PCI. Summary of objective: The QA Specialist I, ACM is a key member of the... ...performance and aseptic behavior, ACM program documentation (including tracking and trending), and... ...safety/efficacy for phase appropriate CGMP manufacture of drug products. Essential Duties...Full timeFlexible hours$75k - $85k
...in patient lives. The Quality Assurance QA Associate II - Quality Events Team (QET) is... ...preventive actions (CAPAs) in compliance with cGMP, SOPs, and regulatory requirements.... ...of quality events. Track and maintain documentation of deviations and CAPAs in compliance with...Work at officeRemote work$85k - $89k
...compliance with regulatory requirements, good manufacturing practices (cGMP), and standard operating procedures. Responsible for... ...pre- and post‑execution batch record review. Author and update documents related to material management quality control, batch records,...Contract work$65k - $70k
Catalent, Inc. in San Diego is hiring a Quality Assurance Associate I, Analytical to ensure compliance with quality standards. The position... ...with HPLC. The successful candidate will review controlled documents and support various manufacturing activities while enjoying...- ...on broad technical skills and QA experience, anticipates and identifies... ...good manufacturing practices (cGMP) and standard operating... ...tested and released Performs document generation and review... ...based approach Support functions associated with the packaging of clinical...
$25 - $31 per hour
...Exempt Non-Exempt Summary It is the responsibility of the Quality Assurance Specialist to assemble assigned departmental reports and documentation related to quality management and performance improvement activities within the Centers for Disease Control, any State, and...Remote workShift work$89.22k - $122.67k
...25. Experience in interpreting regulatory policies and guidance documents and can correctly apply them as appropriate to related activities... ...results on time. Willing to travel 10% - 25%. Relevant QA experience for 3-5 years in a 21 CFR Part 211 or 212 regulated industry...Temporary workLocal area$60k - $85k
...Quality Assurance Associate Reporting to the Quality Assurance Manager, the Quality Assurance... ...Support Quality Assurance (QA) Batch Record Review, Product Disposition... ...party contract organizations to resolve any documentation discrepancies identified during review....Contract work- Position Quality Document Specialist Location San Diego, CA Duration 12 Months Contract Hours 40.00 hours per week Shift 1st shift Description Responsible for efficient and effective performance of testing in conformance with regulations and standards. Inspection...Contract workWork experience placementShift workDay shift
$70.3k - $75.93k
...quality metrics tracking. The role requires a High School Diploma and 3-5 years of relevant experience. Responsibilities include document control, CAPA monitoring, and supporting audits. The hiring rate is between $70,304-$75,928 plus bonuses, along with competitive benefits...$85k - $89k
...of small molecule and peptide drug candidates. Responsibilities Pre- and post-execution batch record review Authoring and updating documents related to Material Management Quality Control, Material Management Quality Assurance, Batch Records, Compliance, and Validation...Monday to Friday- ...Penn Pharmaceutical Services Ltd in San Diego is looking for a QA Specialist I. This role involves real-time monitoring of aseptic... ...include overseeing operator performance, observing and documenting manufacturing activities, and collaborating with multiple departments...Hourly pay
- Sonara Inc. is seeking a Quality Associate for an on-site contract opportunity in San Diego, California. The successful candidate will inspect incoming materials for GMP production and assist with various packaging activities, ensuring compliance with FDA guidelines. Applicants...Contract work
- R&D Partners is seeking to hire a QA Complaint Intake Specialist in San Diego, CA . Your main responsibilities as a QA Complaint... ...channels. Review incoming complaint information and supporting documentation to assess reported events, identify potential complaint...
- ...candidate will possess a Bachelor's degree in a related field, with at least two years of relevant experience. You will play a vital role in continuous improvement efforts while upholding high standards of documentation and member care. #J-18808-Ljbffr Pacific Health Group
- ...performance assessments to the contracting officer for use in determining future awards. Review work specifications and other contract documents to ensure adequate quality requirements are specified. Develop inspection system plans, instructions, and checklists to...Contract workFor contractorsInterim roleImmediate startRemote work
- Travere Therapeutics in San Diego is hiring a Quality Associate to support Quality Operations, overseeing Manufacturing, Packaging, and Labeling... ...of quality records. Ideal candidates should have 2-3 years of QA experience, strong interpersonal skills, and a thorough...
- PCI Pharma Services is hiring a QA Specialist I in San Diego, California. This role is crucial for overseeing aseptic operations,... ...quality assurance operations, and possess excellent observation and documentation skills. The position offers competitive pay and a comprehensive...
- ...key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial... ...documentation. Collaborate cross-functionally with QA, Manufacturing, and external partners to support product...Work at officeShift work
- A remote company is looking for a Data Entry Operator to manage data entry tasks and ensure accurate information documentation. The ideal candidate will have a high school diploma or GED and 5-7 years of experience. Strong verbal and written communication skills, attention...Remote work
- ...quality management professional in San Diego, California. This role involves managing quality systems compliance, drafting regulatory documents, and supporting audits. The candidate should excel in technical writing and possess a strong regulatory judgment. The position...
- ...quality systems, supporting audits, and ensuring compliance with cGMP standards across manufacturing and operations. Key... ...including FDA inspections Maintain and update SOPs, quality documentation, and training records Partner cross-functionally with manufacturing...Full time
- ...We are seeking a Quality Assurance Associate II to join our team. This role is critical... ...production activities, ensuring compliance with cGMP and regulatory standards. The position... ...issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal...Work at office
- ...company maintains necessary regulatory approvals. The role includes managing documentation, compliance operations, and communication with regulatory agencies. Ideal candidates will possess an Associate's degree, be bilingual in English and Spanish, and demonstrate good...
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