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Full Time Msat Engineer Jobs (NOW HIRING)

Lonza

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

The full-time base annual salary for this position is expected to range between $198,900 to $232 ... Working closely with the End-to-End Program Lead, Global Engineering, Quality, MSAT, Manufacturing ...

Lonza

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

The full-time base annual salary for this position is expected to range between $198,900 to $232 ... Working closely with the End-to-End Program Lead, Global Engineering, Quality, MSAT, Manufacturing ...

Lonza

Director, Automation

Walkersville, MD · On-site +1

$203K - $237K/yr

The full-time base annual salary for this position is expected to range between $203,400 to $237 ... Partner with Engineering, Manufacturing, MSAT, Quality, IT/OT, CSV, and EHS teams to ensure ...

Lonza

Director, Automation

Walkersville, MD · On-site +1

$203K - $237K/yr

The full-time base annual salary for this position is expected to range between $203,400 to $237 ... Partner with Engineering, Manufacturing, MSAT, Quality, IT/OT, CSV, and EHS teams to ensure ...

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Full Time Msat Engineer information

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$111.6K

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How much do full time msat engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for full time msat engineer in the United States is $111,632.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $132,500.00 per year, depending on experience, location, and employer.

What is a full time MSAT engineer?

A Full Time MSAT (Manufacturing Science and Technology) Engineer is a professional responsible for supporting manufacturing processes by applying scientific and engineering principles to improve product quality, efficiency, and compliance. They work closely with production, quality assurance, and research teams to optimize manufacturing workflows, troubleshoot issues, and implement process improvements. The role often involves data analysis, process validation, technology transfer, and ensuring that manufacturing operations adhere to regulatory standards. MSAT Engineers play a crucial role in industries such as pharmaceuticals, biotechnology, and chemicals, where maintaining high standards in production is essential.

What are some common challenges a full time MSAT engineer faces when working with satellite communication systems?

As a Full Time Msat Engineer, one of the main challenges is ensuring reliable connectivity in diverse and sometimes harsh environments. Engineers must frequently troubleshoot hardware and software issues, manage signal interference, and adapt to evolving satellite technologies. Collaboration with cross-functional teams such as network operations, field technicians, and system architects is essential to address these challenges efficiently. Additionally, staying updated on regulatory changes and industry standards is crucial for maintaining system compliance and performance.

What are the key skills and qualifications needed to thrive as a full time MSAT engineer, and why are they important?

To thrive as a Full Time MSAT (Manufacturing Science and Technology) Engineer, you need a solid background in chemical engineering, biotechnology, or a related field, typically with a relevant degree and experience in process development or manufacturing. Familiarity with process analytical technology (PAT), data analysis tools, and quality management systems is commonly required, along with knowledge of GMP regulations. Strong problem-solving skills, communication abilities, and teamwork are vital soft skills that set top performers apart in this role. These skills and qualifications are crucial for ensuring efficient technology transfer, process optimization, and compliance in pharmaceutical manufacturing environments.

What is the difference between Full Time Msat Engineer vs RF Engineer?

AspectFull Time Msat EngineerRF Engineer
CredentialsBachelor's in Electrical Engineering or related; certifications like RF or microwave certificationsBachelor's in Electrical Engineering or related; certifications in RF or wireless technologies
Work EnvironmentDesign, testing, and deployment of satellite communication systemsDesign, testing, and optimization of radio frequency systems and wireless networks
Industry UsageSatellite communication, aerospace, defenseTelecommunications, wireless service providers, electronics manufacturing

Full Time Msat Engineers focus on satellite communication systems, while RF Engineers work on radio frequency systems across various wireless technologies. Both roles require similar technical credentials and often operate in overlapping industries, but their specific applications and systems differ.

What cities are hiring for Full Time Msat Engineer jobs?

Cities with the most Full Time Msat Engineer job openings:

What are the most commonly searched types of Msat Engineer jobs?

The most popular types of Msat Engineer jobs are:

What states have the most Full Time Msat Engineer jobs?

States with the most job openings for Full Time Msat Engineer jobs include:

Full Time Msat Engineer jobs near you

Manufacturing Support Specialist

Kashiv Biosciences LLC

Chicago, IL • On-site

Full-time, Other

Medical, Dental, Vision, Life, Retirement

Re-posted 13 days ago

Job description

Position Summary
The Manufacturing Support Specialist is a full-time exempt role supporting GMP manufacturing operations at Kashiv BioSciences, LLC, Chicago, IL.
The Manufacturing Support Specialist provides comprehensive administrative, operational, and quality-system support to the Manufacturing department, reporting directly to the Manufacturing Manager. This role is responsible for authoring and lifecycle management of GMP documentation, such as Batch Records (BR), Deviations (DEV), Corrective and Preventive Actions (CAPA), Change Controls (CC), and trainings in alignment with internal procedures and regulatory expectations.
The Manufacturing Support Specialist plays a key role in ensuring compliant and efficient operations by partnering cross-functionally with Quality Assurance, Quality Control, MSAT, Engineering, and Supply Chain to drive timely closure of quality records, ensure data integrity, and support on-time delivery of manufacturing and quality milestones.
This employee must maintain effective employee relationships, compliance with cGMP and other regulatory and SOP requirements, as well as environmental, health and safety obligations and company policies.
Essential Duties and Responsibilities:
Key responsibilities of the position include, but are not limited to:
Technical Documentation and Documentation Management
  • Author, revise, and review controlled GMP documents including Standard Operating Procedures (SOPs), batch records, and training materials
  • Ensure document accuracy, compliance, and alignment with internal quality standards and applicable regulatory requirements
  • Manage document routing, approval workflows, version control, and archival within the documentation management system

Quality System Execution
  • Support initiation, investigation, and closure of Deviation records, including
    • Data gathering and technical writing of deviation narratives
    • Supporting root cause analysis (e.g., fishbone, 5-Why, 6M)
  • Execute and track CAPA activities, including:
    • Documentation of actions, effectiveness checks, and timelines
    • Coordination with SMEs to ensure sustainable corrective actions
  • Support Change Control (CC) processes, including:
    • Preparation of change documentation and impact/risk assessments
    • Identification of impacted systems, documents, and training n
  • Partner with QA to ensure timely closure and audit readiness of records

Project and Deliverables Management
  • Track and drive on-time completion of manufacturing and quality deliverables, including batch documentation, DEV, CAPA, and CC.
  • Maintain visibility of departmental KPIs (e.g., right-first-time, deviation closure timelines, training compliance)
  • Support continuous improvement initiatives by identifying trends in DEVs, CAPAs, and production performance

Training and Onboarding Support
  • Develop and maintain role-based training curricula and qualification matrices
  • Ensure alignment of training content with approved GMP documentation and current processes.
  • Support effectiveness of training through knowledge transfer and process standardization

Manufacturing and Cleanroom Support
  • Provide hands-on operational support in GMP cleanroom environments during peak demand or special projects. Cleanroom operational support may require working 1st shift or 2nd shift.
  • Ensure strict adherence to aseptic technique, gowning, and cleanroom procedures.
  • Provide daily administrative support, including scheduling, coordination of activities, and preparation of reports.
  • Assist with tracking departmental metrics and compiling data to support operational decision-making
  • Assist with implementation of new systems, tools, and process improvements.

Additional Responsibilities
  • Work with operations team to create a culture of accountability, ownership, and continuous improvement.
  • Respect all safety, laboratory policies, and practices on site.
  • Work across departments and/or sites.
  • Work with process engineers and leadership to align the priorities of the team with those of the department.
  • Able to work independently; shows initiative and able to work with all levels of staff.

Requirements
POSITION REQUIREMENTS AND QUALIFICATIONS
  • Education: Associate's or Bachelor's degree in a scientific, technical or related field
  • Background: Manufacturing, Process Engineering, MSAT, Technical Services, or Quality Assurance
  • Experience: GMP environment with minimum 1-2 years of relevant experience
  • Knowledge: GMP manufacturing required; biologics or biosimilars highly preferred
  • Skills:
  • o Technical writing ability
  • o Proficiency in Microsoft Word, Excel and PowerPoint
  • o Proficiency in electronic document or quality management systems highly
  • preferred
  • o Excellent oral and written communication
  • o Work effectively in fast-paced, cross-functional environment
  • o Attention to detail and commitment to accuracy
  • o Proficiency in electronic document or quality management systems
  • Competencies:
  • o Collaboration and teamwork
  • o Quality and compliance focused
  • o Problem-solving and initiative
  • o Accountability and reliability
  • o Adaptability and flexibility

WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS:
  • General Work Environment: Office, laboratories, cleanroom manufacturing facilities
  • Noise: No extraordinary noise levels.
  • Standing/Lifting: Must be able to move around the facility to reach various equipment; and lift at least 25 lbs.
  • Visual: No extraordinary requirements.
  • Stress: High-paced demanding environment to meet ambitious project goals.
  • Travel: Limited travel

Additional Position Information:
  • Support Specialist hours: Office Hours (08:30AM / 09:30AM to 05:00PM / 06:00PM). Overtime, holidays, and weekends may be required based on requirements.
  • Manufacturing Production shift hours: Shift A (first shift): 06:00 AM to 2:30 PM EST, Shift C (second shift): 2:00 PM to 10:30 PM EST, and Shift D (third shift) 10:00 PM to 6:30 PM EST. Overtime, holidays, and weekends may be required based on requirements.
  • Compensation: This is an exempt FTE position.
  • Manufacturing Support Specialist (1-2 years of experience): $65,000-70,000 with up to 5% discretionary bonus
  • Kashiv BioSciences is able to provide sponsorship support for qualified candidates. Please let us know if you currently require sponsorship or may require sponsorship in the future.
  • Interviews and employment are conducted onsite at our Chicago, IL facility. Candidates should currently reside within a reasonable commuting distance or be planning to relocate to the area.

Benefits/Perks:
  • Medical Insurance - Aetna
    • Prescription Drug Converge Rx
    • Virtual Visits - Aetna/Teladoc
    • Health Savings Accounts (HSA)
    • Flexible Spending Accounts (FSA)
  • Dental Insurance - Aetna
  • Vision Insurance - VSP
  • Life and AD&D Insurance
  • Disability Benefits
  • Supplemental Benefits
    • Legal Services
    • ID Theft Protection
    • Travel Assistance
  • Value Added Benefits & Services
    • Health Advocate
    • Life Assistance Program (LAP)
    • Student Loan Assistance Program
  • 401K
  • Monthly Cell Phone Allowance
  • Free Parking (Company Paid)
  • Conveniently located next to the Metra, Green and Red Line
  • One block east of the Chicago White Sox Stadium
  • < 10 minutes away from Downtown Chicago

Supervisory Responsibility, if any : No
This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.
Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, and transfer, leaves of absence, compensation, and training.

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