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Pinnaql

CQV Specialist - Sterilization / SIP

Juncos, PR ยท On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... CQV Specialist Sterilization / SIP Job Summary: We are seeking an experienced CQV Specialist ...

Analog Devices

SiP Layout Design Engineer

Wilmington, MA ยท On-site

$116K - $160K/yr

We are looking for an experienced and detail-oriented SiP layout design engineer with strong expertise in laminate and PCB layout design for advanced semiconductor packaging applications. This role ...

Analogdevices

SiP Layout Design Engineer

Wilmington, MA ยท On-site

$116K - $160K/yr

We are looking for an experienced and detail-oriented SiP layout design engineer with strong expertise in laminate and PCB layout design for advanced semiconductor packaging applications. This role ...

Analog Devices, Inc.

$116K - $160K/yr

We are looking for an experienced and detail-oriented SiP layout design engineer with strong expertise in laminate and PCB layout design for advanced semiconductor packaging applications. This role ...

Loenbro

SIP Estimator

Westminster, CO ยท On-site

SIP Estimator (Scaffolding, Insulation & Painting) Company: Loenbro, LLC Business Unit/Department ... Bachelor's degree in construction management, Engineering, or related discipline * Scheduling ...

Loenbro

SIP Estimator

Westminster, CO ยท On-site

SIP Estimator (Scaffolding, Insulation & Painting) Company: Loenbro, LLC Business Unit/Department ... Bachelor's degree in construction management, Engineering, or related discipline * Scheduling ...

BloKchain Talent

Telephony Engineer

Tempe, AZ ยท On-site

Administration of SIP and Media Servers. * Design and Deploy SIP VOIP trunking architecture. * Telephony Engineer manages 3rd party telecom carriers and mobile providers. Qualifications Requirements:

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How much do sip engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for sip engineer in the United States is $101,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is a SIP engineer?

A SIP Engineer is responsible for designing, implementing, and maintaining Session Initiation Protocol (SIP)-based communication systems. They work with VoIP technology, troubleshoot network issues, and ensure seamless integration of SIP services with existing telecommunication infrastructure. SIP Engineers collaborate with network administrators, developers, and vendors to optimize call quality, security, and system performance. Their role often includes configuring SIP trunks, monitoring traffic, and resolving service outages.

What are the typical daily responsibilities of a SIP engineer?

A SIP Engineer's daily tasks often include configuring, monitoring, and troubleshooting SIP-based communication systems, supporting VoIP infrastructure, and working on system integration with various platforms. They collaborate closely with network engineers, support teams, and sometimes clients to resolve complex issues, ensure call quality, and implement new features. Documentation, testing, and proactive network analysis are also regular parts of the role to help maintain optimal performance. This blend of technical and collaborative work offers variety each day and the opportunity to have a direct impact on critical business communications.

What are the key skills and qualifications needed to thrive in the SIP engineer position, and why are they important?

To excel as a SIP Engineer, you need a solid background in telecommunications networking, a deep understanding of Session Initiation Protocol (SIP), VoIP technologies, and often a degree in computer science or a related field. Experience with SIP protocol analyzers, network monitoring tools, and certifications such as CCNA or relevant VoIP certifications are commonly required. Outstanding troubleshooting skills, clear communication, and the ability to work effectively under pressure help set top performers apart. Mastery of these skills is critical to ensuring reliable and scalable communication services in dynamic telecom environments.

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Sip Engineer jobs near you
Infographic showing various Sip Engineer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $101,752 per year, or $48.9 per hour.

CQV Specialist - Sterilization / SIP

Juncos, PR โ€ข On-site

Pinnaql
Pharmaceutical and Medicine Manufacturingย โ€ขย 11 - 50 employees
Learn more about Pinnaqlexternal

Full-time

Posted 9 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • CQV Specialist๏ฟฝ Sterilization / SIP

Job Summary:
We are seeking an experienced CQV Specialist ๏ฟฝ Sterilization / SIP to support sterilization qualification activities associated with the introduction of a biologics drug substance process into an existing GMP manufacturing facility in Juncos, Puerto Rico.
The individual will support development and execution of sterilization qualification protocols, including SIP and applicable autoclave activities, thermometric studies, biological indicator studies, process-data evaluation, conditional release, discrepancy resolution, and final reporting.
Key Responsibilities
  • Develop and execute sterilization qualification protocols.
  • Support SIP qualification activities for upstream and downstream manufacturing systems.
  • Support qualification of new or impacted autoclave cycles and loads where applicable.
  • Review system design, sequence of operations, operational parameters, manufacturing procedures, equipment documentation, and associated recipes.
  • Identify critical and non-critical sterilization parameters.
  • Support thermometric qualification studies.
  • Prepare and handle biological indicators as required by approved protocols.
  • Coordinate instrumentation, thermocouples, equipment availability, and execution logistics.
  • Coordinate activities with Manufacturing, Engineering, QC, EHS, Quality, and CQV personnel.
  • Evaluate sterilization-cycle process data including:
    • Temperature profiles
    • Exposure times
    • Lethality
    • Flow and process conditions
    • Other protocol-defined parameters
  • Generate and evaluate PI Historian / PI ProcessBook trend charts.
  • Analyze cycle data against protocol acceptance criteria by the end of the applicable working shift.
  • Support sterilization Conditional Release activities.
  • Immediately identify and communicate unexpected results or protocol discrepancies.
  • Support technical investigations, deviations, and corrective actions.
  • Prepare and route sterilization qualification reports for review and approval.
  • Participate in peer review of calculations and technical data.
  • Support night, weekend, or continuous manufacturing schedules when required.

Required Qualifications
  • Bachelor's degree in Engineering, Science, Microbiology, Biotechnology, or related technical field.
  • CQV or validation experience within a GMP pharmaceutical or biotechnology facility.
  • Hands-on sterilization qualification experience.
  • Experience with SIP and/or autoclave qualification.
  • Knowledge of thermometric qualification methodologies.
  • Experience using biological indicators during sterilization studies.
  • Understanding of sterilization-cycle parameters and lethality concepts.
  • Experience generating and executing protocols and preparing final reports.
  • Strong GMP documentation and technical-writing capabilities.

Preferred Qualifications
  • Experience supporting biologics drug-substance manufacturing.
  • Previous Amgen CQV or verification experience.
  • Experience with OSIsoft PI / PI ProcessBook or PI Historian.
  • Experience supporting deviation investigations.
  • Experience with Kneat, LIMS, MAXIMO, Smartsheet, LMS, or equivalent systems.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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