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Osp Quality Control Engineer Jobs in California (NOW HIRING)

Avid Bioservices

Lead Engineer, Quality Control

Tustin, CA · On-site

$105K - $124K/yr

The Lead Engineer, Quality Control shall provide technical validation support for processes, equipment, networks, software that has been newly installed, upgraded, replaced and modified in Quality ...

New

Clera

Research Engineer, QC Automation

San Francisco, CA · On-site

$150K - $250K/yr

About the Role An early-stage AI infrastructure company is hiring a Research Engineer, QC Automation - the #1 priority hire on the engineering team right now. You'll own end-to-end automation of ...

Clera

Research Engineer, QC Automation

San Francisco, CA · On-site

$150K - $250K/yr

About the Role An early-stage AI infrastructure company is hiring a Research Engineer, QC Automation -- the #1 priority hire on the engineering team right now. You'll own end-to-end automation of ...

Joby Aviation

Quality Control Manager

San Carlos, CA

$95K - $195K/yr

This is a hands-on, floor-level Quality Control & Inspection leadership role; not a Design Engineering or Quality Engineering position. Candidates must have direct experience supervising or managing ...

Joby Aviation

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

This is a hands-on, floor-level Quality Control & Inspection leadership role; not a Design Engineering or Quality Engineering position. Candidates must have direct experience supervising or managing ...

Joby Aviation

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

This is a hands-on, floor-level Quality Control & Inspection leadership role; not a Design Engineering or Quality Engineering position. Candidates must have direct experience supervising or managing ...

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All JobsOsp Quality Control Engineer JobsOsp Quality Control Engineer Jobs in California

Osp Quality Control Engineer information

What are the key skills and qualifications needed to thrive as an OSP Quality Control Engineer?

To thrive as an OSP (Outside Plant) Quality Control Engineer, you need a strong understanding of telecommunications infrastructure, construction standards, and quality assurance processes, often supported by a degree in engineering or a related field. Familiarity with GIS mapping tools, fiber optic testing equipment, and industry standards like TIA/EIA or ISO certifications is typically required. Attention to detail, problem-solving, and effective communication are vital soft skills for ensuring project requirements are met and collaborating with contractors. These skills and qualifications are crucial for maintaining network integrity, ensuring compliance, and delivering reliable telecom services.

What is the difference between Osp Quality Control Engineer vs Quality Assurance Technician?

AspectOsp Quality Control EngineerQuality Assurance Technician
CertificationsISO, Six Sigma, industry-specific standardsISO, Six Sigma, industry standards
Work EnvironmentManufacturing, construction, industrial sitesManufacturing plants, labs, inspection sites
Primary FocusInspecting and testing products/processes for complianceDeveloping and implementing quality procedures

Osp Quality Control Engineers focus on inspecting and testing products to ensure compliance with standards, often working on-site in manufacturing or industrial environments. Quality Assurance Technicians primarily develop and implement quality procedures to prevent defects. Both roles require similar certifications and are integral to quality management in industries like manufacturing and construction.

What does an OSP Quality Control Engineer do?

An OSP (Outside Plant) Quality Control Engineer is responsible for ensuring that the installation, maintenance, and operation of telecommunications infrastructure outside central facilities—such as fiber optic cables, conduits, and related equipment—meet industry standards and project specifications. They conduct inspections, review construction work, and verify compliance with quality, safety, and regulatory requirements. Their work is crucial for maintaining network reliability and performance, often involving collaboration with contractors, project managers, and field technicians. OSP Quality Control Engineers also document issues, recommend corrective actions, and help implement best practices to prevent future problems.

What are some typical challenges faced by OSP Quality Control Engineers in the telecommunications industry?

OSP Quality Control Engineers often encounter challenges such as ensuring that contractors adhere strictly to design specifications and industry standards during the installation of outside plant (OSP) infrastructure. They must also manage tight project deadlines and coordinate with multiple teams, including construction, design, and project management. Regular site inspections are required to detect and resolve issues early, and effective communication is essential to address discrepancies quickly. Staying updated on evolving technologies and regulatory requirements is also crucial for success in this role.
What are popular job titles related to Osp Quality Control Engineer jobs in California? For Osp Quality Control Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Osp Quality Control Engineer jobs in California look for? The top searched job categories for Osp Quality Control Engineer jobs in California are:
What cities in California are hiring for Osp Quality Control Engineer jobs? Cities in California with the most Osp Quality Control Engineer job openings:
Osp Quality Control Engineer jobs near you
Infographic showing various Osp Quality Control Engineer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Lead Engineer, Quality Control

Avid Bioservices

Tustin, CA • On-site

$105K - $124K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Lead Engineer, Quality Control shall provide technical validation support for processes, equipment, networks, software that has been newly installed, upgraded, replaced and modified in Quality Control. This role is the primary interface with Quality Control for Validations and Facilities on QC equipment.
Key Responsibilities:
  • Take on lead role for select Capex and Opex projects within the QC department. This includes planning, project management, proposal, budgeting, and execution.
  • Plan and procure new QC equipment as required.
  • Plan and coordinate laboratory movement of QC equipment.
  • Generate and review relevant documents for new equipment
  • Schedule and manage routine PM on QC equipment
  • Assess equipment needs for QC and manage equipment purchasing process
  • Write and manage Engineering Change Request (ECR) documents
  • Author User Requirement Specification (URS) and/or Requirement Specification documents for quality control equipment/systems and processes
  • Generate and execute Installation, Operational and Performance/Process qualification (IQ, OQ, PQ) protocols and final reports that comply with corporate and regulatory requirements
  • Coordinate and oversee validation protocol execution or validation activities
  • Evaluate and analyze qualification data collected during projects while verifying acceptability of the data and compliance with the approved protocol
  • Ensure any deviations to protocols and/or deviations to acceptance criteria are adequately addressed, documented and reviewed
  • Improve validation and equipment processes
  • Assist department manager in developing realistic time and resource requirements for validation activities in support of company expectations
  • Provide input and assist in change control assessment and Part 11 assessment for validated systems
  • Review Standard Operating Procedures (SOPs) and ensure the operational parameters described in the SOP for the equipment reflect validated conditions
  • Assist department manager on other types of projects/managerial responsibilities as needed
  • Schedule and manage routine instrument PM processes
  • Occasional overnight travel by land and/or air may be required to attend seminars or conferences or client meetings
  • Perform other duties as assigned

Minimum Qualifications:
  • Requires a BA/BS in Science (such as Biology, Microbiology, Biochemistry, Chemistry) or other technologically related field plus 4-5 years' work experience in a biopharmaceutical/pharmaceutical manufacturing environment of which 3 years were directly involved in validations.
  • Must have knowledge of validation principles, standard concepts, practices, procedures and requirements in a GMP regulated environment.
  • An understanding of Good Automated Manufacturing Practice (GAMP), SDLC, Risk Assessment and 21 CFR Part 11 Electronic Records and Electronic Signatures required.

Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $105,000 - $124,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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