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Full Time Msat Engineer Jobs (NOW HIRING)

Lonza

Director, MSAT

Walkersville, MD · On-site +1

$205K - $239K/yr

The full-time base annual salary for this position is expected to range between $205,200 to $239 ... The Director will work closely with Engineering, Manufacturing, Quality, Automation, EHS, and ...

Lonza

Director, MSAT

Walkersville, MD · On-site +1

$205K - $239K/yr

The full-time base annual salary for this position is expected to range between $205,200 to $239 ... The Director will work closely with Engineering, Manufacturing, Quality, Automation, EHS, and ...

Ocular Therapeutix

Process Engineer, MSAT

Bedford, MA · On-site

$94K - $125K/yr

... Technology (MSAT) department. This engineer will join a team in the clinical and commercial ... This position will be based full-time onsite in Bedford, MA. Principal Duties and Responsibilities

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

The full-time base annual salary for this position is expected to range between $174,600 to $203 ... Partner with Engineering, Manufacturing, Quality, Automation, and EHS teams to ensure process ...

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

The full-time base annual salary for this position is expected to range between $174,600 to $203 ... Partner with Engineering, Manufacturing, Quality, Automation, and EHS teams to ensure process ...

Avid Bioservices

Engineer, MSAT Upstream

Tustin, CA · On-site

$95K - $119K/yr

As an Engineer, MSAT Upstream at Avid Bio, you will be the main point of contact for clients and ... This role is a full-time position. Days of work are Monday through Friday. The employee must also ...

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Full Time Msat Engineer information

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$59.5K

$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

Process Engineer, MSAT

Ocular Therapeutix

Bedford, MA

Full-time

Re-posted 11 days ago

Job description

Position Summary:

This position will serve as a mid-level engineer focused on drug product and process development in the Manufacturing Sciences and Technology (MSAT) department. This engineer will join a team in the clinical and commercial development of the processes used to manufacture sustained release hydrogel drug products. This role includes but is not limited to experimental design, process development, packaging, inspection and material characterization. This individual will execute some assigned project activities, lead some project activities, and work with team members to improve, evaluate, and develop the products and their associated processes. This engineer will be supporting the integration of a drug product with a medical device to produce a combination product. The position is set in a dynamic and fast-paced environment at a growing company.

Critical areas of focus will be in experimental design, laboratory work, testing, technical transfers, scale-up and new process development. Incorporation of automation into a complex manual process will be another area of focus for this engineer. This position will be based full-time onsite in Bedford, MA.

Principal Duties and Responsibilities:

  • Design, develop, execute and characterize process development studies.
  • Design and develop unit operations of a scalable commercial manufacturing process.
  • Execute improvement of current clinical and commercial manufacturing activities.
  • Implement and integrate automated systems into a complex manual process.
  • Assist in the cGMP manufacturing of drug product batches in clean room environment to support clinical studies.
  • Understand GMP regulation and FDA/EMEA guidance on manufacturing processes and apply them during manufacturing of combination product batches.
  • Analyze and evaluate the impact of process variables on combination product characteristics.
  • Communicate study designs, data analysis and conclusions to project team members.
  • Generate technical documents including protocols and reports summarizing experimental plans and test results.
  • Collaborate effectively with MSAT group and project team members.
  • Serve as an MSAT SME in cross-functional interactions with other departments.
  • Demonstrate an understanding of late-stage combination product development and tech transfer needs of commercial development.

Requirements:

  • Minimum of a bachelor's degree (advanced degree desirable) in Chemical Engineering, Biomedical Engineering, Mechanical Engineering or related discipline.
  • 4+ years of biopharma industry experience in drug or combination process development.
  • Prior experience working within a cGMP manufacturing environment.
  • Ability to apply fundamental scientific and engineering skills to evaluation of processes and development of practical solutions to technical challenges.
  • Experience creating technical, written content.
  • Demonstrated written and verbal communication skills.
  • Demonstrated data analysis and problem-solving skills.
  • High degree of initiative and self-motivation.
  • A diligent team-player that is passionate about helping patients and effectively collaborates in a dynamic, cross-functional environment.
  • Experience with generic lab equipment (Ex. pipettes, balances, pumps, microscopes) is preferred.
  • Experience with automated or manual inspection systems is preferred.

Working Conditions:

  • Production Floor - gowning/cGMP requirements.
  • Laboratory/Clean Room - bending/lifting requirements.

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