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Remote Textile Quality Control Jobs in California

Amgen

Associate Quality Control

Thousand Oaks, CA · On-site +1

Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Flexible work models, including remote and hybrid work arrangements, where possible Apply now and ...

Visby Medical

Director of Quality

San Jose, CA · Remote

Ensure efficient and effective quality control processes and procedures, including use of ... validation in remote or outsourced manufacturing environments. Willingness to travel ...

Parallax Creative

Rhino/Revit BIM QA Lead

Los Angeles, CA · Remote

$400 - $600/day

An estimated 15-26 weeks of remote, full-time production. Responsibilities Own the Rhino-to-Revit validation and quality control pipeline Establish and enforce modeling, layer, naming, and file ...

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All JobsTextile Quality Control JobsRemote Textile Quality Control JobsRemote Textile Quality Control Jobs in California

Remote Textile Quality Control information

What are the three types of textile industry?

The textile industry is generally divided into three main types: fiber production, fabric manufacturing, and apparel or product manufacturing. A remote textile quality control professional may focus on ensuring quality standards across these stages, particularly in fabric and product inspection. Understanding these segments helps in assessing quality and compliance throughout the supply chain.

What is the difference between Remote Textile Quality Control vs Remote Textile Production Assistant?

AspectRemote Textile Quality ControlRemote Textile Production Assistant
CredentialsQuality certifications, attention to detailBasic industry knowledge, organizational skills
Work EnvironmentMonitoring and inspecting textiles remotely, using digital toolsSupporting production tasks, coordinating with teams remotely
Industry UsageQuality assurance in textile manufacturingAssisting production processes in textile companies
Search IntentQuality control, inspection, complianceProduction support, coordination roles

Remote Textile Quality Control focuses on inspecting and ensuring textile quality remotely, often requiring certifications and attention to detail. In contrast, Remote Textile Production Assistants support production workflows and coordination tasks. Both roles are essential in the textile industry but serve different functions in the manufacturing process.

Is quality control still a job?

Yes, quality control remains a vital role in the textile industry, including remote positions focused on inspecting and ensuring product standards. These jobs often require attention to detail, knowledge of textile materials, and sometimes certification or training in quality management systems.

What are the 7 tools of quality control in garment industry?

In the garment industry, including roles like remote textile quality control, the 7 tools of quality control are Pareto charts, fishbone diagrams, control charts, histograms, scatter diagrams, check sheets, and flowcharts. These tools help identify defects, analyze root causes, and monitor process performance to ensure product quality. Proficiency in these tools supports effective quality management and continuous improvement.

What are some common challenges faced in a remote textile quality control role, and how can they be addressed?

One of the main challenges in remote textile quality control is ensuring accurate product assessments without being physically present on-site. This often requires effective use of digital tools, high-quality images, and clear communication with on-site teams. Building strong relationships with local staff, setting up standardized reporting procedures, and leveraging video calls for virtual inspections can help overcome these obstacles. Staying organized and adaptable is key, as each factory or supplier may have different workflows and quality standards.

What are the key skills and qualifications needed to thrive as a Remote Textile Quality Control specialist, and why are they important?

To thrive as a Remote Textile Quality Control specialist, you need a thorough understanding of textile materials, quality assurance standards, and inspection techniques, often supported by a degree in textiles or related experience. Familiarity with digital quality management systems, textile testing equipment, and remote inspection software is typically required. Strong attention to detail, effective communication, and problem-solving abilities are crucial soft skills for this role. These skills ensure accurate quality assessments, minimize defects, and maintain production standards across geographically dispersed manufacturing operations.

Is a textiles degree worth it?

A textiles degree can be valuable for a remote textile quality control role, as it provides knowledge of fabric properties, manufacturing processes, and quality standards. However, practical experience, attention to detail, and familiarity with testing tools are also highly important in this field. The degree may enhance job prospects but is not always mandatory if relevant skills are demonstrated.

What is a Remote Textile Quality Control specialist?

A Remote Textile Quality Control specialist is responsible for ensuring that fabrics and textile products meet established quality standards while working from a remote location. They review samples, analyze data, and communicate with manufacturers, suppliers, and clients to identify any defects or inconsistencies in textile products. Their main tasks may include inspecting product images or videos, reviewing documentation, and using digital tools to monitor quality throughout the production process. This role helps companies maintain product consistency and compliance without the need for on-site inspections.
What are the most commonly searched types of Textile Quality Control jobs in California? The most popular types of Textile Quality Control jobs in California are:
What are popular job titles related to Remote Textile Quality Control jobs in California? For Remote Textile Quality Control jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Textile Quality Control jobs in California look for? The top searched job categories for Remote Textile Quality Control jobs in California are:
What cities in California are hiring for Remote Textile Quality Control jobs? Cities in California with the most Remote Textile Quality Control job openings:
Remote Textile Quality Control jobs near you

Director, Quality Control

Oruka Therapeutics

Menlo Park, CA • On-site, Remote

Full-time

Posted 20 days ago

Job description

About Us:
Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Job Title: Director, Quality Control
Location: Hybrid - Waltham, MA or Menlo Park, CA. Candidates will be required to be in-office 3 days/week Open to remote for non-local candidates.
Role Overview:
The Director, Quality Control - Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. This role will ensure timely, compliant, and scientifically sound oversight of release, stability, characterization, in-process, and method lifecycle activities performed at CMOs and contract testing laboratories.
This role is responsible for ensuring that all QC systems, analytical methods, and testing programs are inspection-ready and aligned with global regulatory expectations for commercial biologics. The Director will partner cross-functionally and externally to enable successful PPQ execution, analytical method validation, regulatory approval, and commercial launch readiness.
Key Responsibilities:
QC Strategy, Clinical Execution & Commercial Readiness
  • Develop and execute the enterprise QC strategy to support clinical product testing, Phase 3 clinical trials, PPQ, BLA submission, and commercial launch.
  • Build scalable QC systems, processes, governance, and organizational capabilities aligned with commercial-stage operations.
  • Establish and maintain analytical control strategies for drug substance (DS), drug product (DP), and combination products.
  • Ensure inspection readiness across QC operations, documentation, data integrity, and external partner networks.
  • Serve as a strategic advisor to Quality and CMC on analytical and QC-related risks, compliance considerations, and commercialization readiness.

Analytical Methods, Validation & Lifecycle Management
  • Lead and provide oversight of analytical method qualification, validation, transfer, verification, and lifecycle management in alignment with ICH, FDA, EMA, and global regulatory expectations.
  • Ensure all release, characterization, and stability-indicating methods are validated and commercially sustainable prior to BLA submission.
  • Oversee analytical comparability strategies, method bridging activities, and technology transfers across CMOs and contract laboratories.
  • Drive continuous improvement of analytical control strategies and testing programs through data trending and lifecycle management principles.
  • Ensure effective governance of reference standards, critical reagents, and assay performance monitoring programs.

PPQ, Validation & Continued Process Verification
  • Partner cross-functionally with Manufacturing, MSAT, and CMC teams to ensure QC readiness for PPQ execution and commercial manufacturing.
  • Provide QC oversight for in-process, release, and stability testing supporting validation campaigns and commercial supply.
  • Support continued process verification (CPV) programs through statistical trending, data analysis, and ongoing monitoring of product quality attributes.
  • Ensure timely and compliant batch disposition support through robust data review and issue escalation processes.

Combination Product Quality Control Leadership
  • Lead QC strategy and oversight for combination products, including pre-filled syringes, autoinjectors, and device constituent components.
  • Ensure compliant testing strategies for container closure integrity, product-device compatibility, particulate matter, functionality, and device-related attributes.
  • Oversee QC support for extractables and leachables (E&L), shipping validation, and stability programs associated with delivery systems.
  • Ensure QC operations and external partners comply with applicable combination product regulations, including 21 CFR Part 4 and relevant global guidance.
  • Support commercial readiness and lifecycle management for combination product manufacturing and release.

Clinical Product Analytical Testing Oversight and External Laboratory Management
  • Provide QC oversight for analytical testing of clinical drug substance and drug product, including release, stability, in-process, characterization, and comparability testing.
  • Provide oversight of contract testing laboratories and CMOs, including selection, qualification, governance, performance management, and risk mitigation.
  • Establish and maintain Quality Agreements and analytical governance structures aligned with commercial and regulatory expectations.
  • Lead oversight activities during critical manufacturing campaigns, investigations, audits, and inspection preparation activities.
  • Drive accountability and performance across the external analytical network to ensure reliable execution and compliance.
  • Investigations, Compliance & Quality Systems
  • Lead complex investigations involving OOS, OOT, deviations, laboratory events, complaints, and analytical discrepancies.
  • Ensure robust root cause analysis, effective CAPA implementation, and sustainable compliance solutions.
  • Champion data integrity principles (ALCOA+) and ensure compliance across QC systems, laboratories, and third-party partners.
  • Establish meaningful QC metrics, dashboards, and management review processes to drive operational excellence and continuous improvement.

Regulatory & Inspection Support
  • Author, review, and approve QC-related sections of regulatory submissions, including analytical methods, specifications, validation reports, comparability assessments, and stability data.
  • Serve as the QC Subject Matter Expert during regulatory inspections, pre-approval inspections (PAIs), and partner audits.
  • Lead responses to health authority questions, observations, and deficiency letters related to analytical and QC activities.
  • Maintain current knowledge of evolving global regulatory expectations for biologics and combination products.

Qualifications:
Required
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related scientific discipline; advanced degree preferred.
  • 10+ years of progressive Quality Control and analytical experience within GMP biopharmaceutical environments, including late-stage clinical and commercial readiness activities.
  • Experience overseeing GMP analytical testing for clinical-stage biologic DS and DP, including release, stability, in-process, and/or comparability testing performed by CMOs or contract testing laboratories.
  • Demonstrated experience supporting BLA and/or MAA submissions, regulatory inspections, and commercial launch preparation.
  • Deep expertise in biologics analytical methods, including chromatographic, electrophoretic, cell-based, compendial, and microbiological techniques.
  • Extensive experience with analytical method validation, lifecycle management, comparability, and technology transfer.
  • Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4.
  • Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.
  • Proven success leading QC support for PPQ campaigns, validation activities, and commercial manufacturing readiness.
  • Demonstrated experience managing CMOs, contract laboratories, and global external testing networks.
  • Strong understanding of data integrity principles, electronic systems, and QC compliance requirements.
  • Proven ability to build and scale Quality organizations in a fast-paced biotech environment.
  • Excellent leadership, communication, and cross-functional collaboration skills with the ability to influence at all organizational levels.

Preferred
  • Direct experience supporting successful BLA approval and commercial product launch.
  • Experience in a rapidly growing biotechnology company transitioning to commercial operations.
  • Knowledge of extractables/leachables, container closure systems, and device constituent testing.
  • Experience implementing or optimizing LIMS, stability systems, and digital QC infrastructure.
  • Experience supporting global regulatory filings and international commercialization activities.

Compensation:
  • An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
  • The anticipated salary range is $213,000 - $240,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.

Location: Hybrid - Waltham, MA or Menlo Park, CA. Candidates will be required to be in-office 3 days/week Open to remote for non-local candidates
We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.
Salary Range for the Role
$213,000-$240,000 USD
What We Offer:
  • A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
  • Competitive salary and benefits package.
  • A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
  • Opportunities for professional growth and development.

Apply