Quality Systems Specialist

Sanisure Llc; Camarillo (CA); On-site; USD 70,000 - 75,000; Full time

Job summary

SaniSure is seeking a Quality Systems Specialist to support and maintain the Quality Management System in Camarillo, CA. You will oversee creation, review, and controlled release of quality and technical documentation including SOPs, specifications, and validation data.

The role works cross-functionally with Quality, Engineering, R&D/NPI, Regulatory Compliance, Manufacturing, and Supply Chain to ensure accurate, traceable, and compliant product information throughout the lifecycle.

Qualifications

• 3+ years' experience in quality systems within regulated manufacturing.
• Experience with risk management tools (FMEA) and CAPA methods.
• Knowledge of QMS and document-control practices.
• Experience creating, reviewing, and maintaining controlled documents.
• Ability to interpret drawings, specs, and component information.
• Experience with supplier qualification and quality improvements.

Responsibilities

• Develop, review, approve, and maintain quality documentation and records.
• Coordinate collection of product/component information including specs and compliance data.
• Maintain revision history, traceability, and controlled release processes.
• Support internal/supplier audits and CAPA activities.
• Monitor quality trends and drive improvements across the QMS.

Skills

Quality systems

Documentation control

CAPA/root cause

FMEA

QMS principles

Document-control practices

Audits

Technical documentation

Supplier qualification

Detail oriented

Education

Bachelor's degree in biological sciences, engineering, or related field

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Systems Specialist

Regular - Full Time Camarillo, CA, US

Salary Range: $70,000.00 To $75,000.00 Annually

About SaniSure

SaniSure is a high-growth multinational manufacturer of single-use products and systems used in the production of biological drugs, including cell therapies, gene therapies, and vaccines. With operations in the U.S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they need to develop and manufacture some of today's most innovative and life-changing medicines.

As we continue to expand our product offerings and global footprint, SaniSure offers an exciting opportunity to join a nimble, customer-focused company at the forefront of the biotech industry.

Job Summary

The Quality Systems Specialist supports and maintains the Quality Management System (QMS) and oversees the creation, review, approval, revision, and controlled release of quality and technical product documentation including, but not limited to, validation guides, assembly component summaries, component attributes, specifications, validation and compliance documentation, certificates, and related quality records.

The position works cross-functionally with internal teams including Quality, Engineering, R&D/NPI, Regulatory Compliance, Manufacturing, and Supply Chain, as well as external suppliers and customers, to ensure product information is accurate, complete, traceable, and compliant with established quality requirements.

Essential Functions

• Develop, compile, review, approve, revise, and maintain controlled quality and technical documentation, including SOPs, specifications, forms, validation guides, and related records.
• Coordinate the collection and verification of product and component information, including drawings, part numbers, materials, suppliers, manufacturers, compliance information, validation data, sterilization information, shelf life, and storage conditions.
• Ensure documentation accurately reflects approved product configurations and is consistent with drawings, specifications, supplier information, and quality records.
• Maintain document revision history, traceability, templates, workflows, and controlled release processes.
• Identify and resolve missing, outdated, inconsistent, or conflicting information with appropriate functional owners.
• Oversee product-specific technical documentation packages supporting customer evaluation, qualification, and validation.
• Coordinate supporting documentation such as component attributes, raw material and manufacturer specifications, validation guides, assembly drawings, Certificates of Conformance, sterilization certificates, and applicable compliance documentation.
• Maintain applicable material, biocompatibility, extractables, regulatory, and sterilization information and ensure information is traceable to the appropriate component and product configuration.
• Support nonconformance investigations, root cause analysis, CAPA, quality improvement activities, and effectiveness verification.
• Assist with internal and supplier audits and support supplier qualification activities.
• Monitor quality information and trends and identify opportunities to improve QMS and documentation processes.
• Support customer and external audits by providing accurate, current, and controlled quality and technical documentation.
• Evaluate changes to products, components, materials, suppliers, specifications, drawings, and validation documentation for impact on controlled documents.
• Coordinate updates to affected validation guides, assembly component summaries, specifications, and supporting records.
• Ensure obsolete information is appropriately controlled and revised documentation reflects the approved product configuration.
• Support product transfers, validation activities, and other quality projects throughout the product lifecycle.
• Respond to customer requests for quality, technical, compliance, and validation documentation, including surveys and questionnaires.
• Coordinate with Engineering, R&D/NPI, Regulatory Compliance, Operations, Manufacturing, Supply Chain, Quality, suppliers, and customers to obtain and verify information.
• Track documentation activities, action items, timelines, risks, and outstanding requirements, and quality processes.
• Perform other tasks as assigned.

Education/Certifications

• Bachelor's degree in biological sciences, engineering, or a related technical field.

Required Experience & Competencies

• 3+ years' experience in quality systems, quality documentation, technical documentation, or quality management in a regulated manufacturing environment.
• Experience with risk management tools (FMEA) and CAPA/root cause methodologies.
• Working knowledge of QMS principles and document-control practices.
• Experience developing, reviewing, maintaining, and implementing controlled documents.
• Experience coordinating technical information from multiple internal and external sources.
• Experience with nonconformance, CAPA, investigations, audits, supplier qualification, or quality improvement activities.
• Ability to understand and review product drawings, specifications, component information, and validation documentation.
• Strong attention to detail, organization, analytical, and problem-solving skills.
• Ability to identify incomplete, inconsistent, or conflicting technical information and coordinate resolution.
• Strong written and verbal communication skills with the ability to prepare clear, accurate technical documentation.
• Familiarity with biocompatibility, extractables, sterilization, and regulatory compliance documentation.
• Experience with supplier technical documentation and qualification programs.

Equal Employment Opportunity Policy

We are committed to providing equal employment opportunities to all employees and applicants without regard to race, religion (including religious dress and grooming practices), color, sex (including childbirth, breast feeding, and related medical conditions), gender identity or expression, sexual orientation, national origin, citizenship status, uniform service member status, pregnancy, age (40 and over), genetic information, disability (mental and physical), or any other protected status in accordance with all applicable federal, state, and local laws.