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Contract Msat Process Engineer Jobs in Raleigh, NC

GlaxoSmithKline

MES Solution Specialist

Zebulon, NC · On-site

$110 - $160/hr

... Process Checks (IPC), and Serialization. Working closely with MSAT, Manufacturing, Quality, Engineering, Supply Chain, Digital, and other stakeholders, the MES Solutions Specialist translates ...

GlaxoSmithKline

MES Solution Specialist

Zebulon, NC

... Process Checks (IPC), and Serialization. Working closely with MSAT, Manufacturing, Quality, Engineering, Supply Chain, Digital, and other stakeholders, the MES Solutions Specialist translates ...

Kaygen Inc.

Engineer3, Process Validation

Durham, NC · On-site

Durham NC Duration: 12-month contract On site, 5 days at week, Industrial Engineer This position is ... processes. · Drive initiatives focused on improving manufacturing profitability, labor ...

GSK

MES Solution Specialist

Zebulon, NC · On-site

... Process Checks (IPC), and Serialization. Working closely with MSAT, Manufacturing, Quality, Engineering, Supply Chain, Digital, and other stakeholders, the MES Solutions Specialist translates ...

Fujifilm

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Cross-Functional Collaboration - partners with Manufacturing and MSAT/Engineering on facility ... Experience supporting or executing validation for sterilization, aseptic processing (media fills ...

Fujifilm

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Cross-Functional Collaboration - partners with Manufacturing and MSAT/Engineering on facility ... Experience supporting or executing validation for sterilization, aseptic processing (media fills ...

Hitachi, Ltd.

Contract Management Professional

Raleigh, NC · On-site

$86K - $115K/yr

Drive change management processes for contract modifications. * Oversee project closeout and ensure ... Strong knowledge of engineering, procurement, and service agreements. * Proven ability to manage ...

Visium Resources, Inc.

Be Seen First

Electrical Engineer

Raleigh, NC · On-site

Supervise contractors during critical installations of process equipment and associated utilities ... Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe ...

Hitachi

Contract Management Professional

Raleigh, NC · On-site +1

$86K - $115K/yr

Drive change management processes for contract modifications. * Oversee project closeout and ensure ... Strong knowledge of engineering, procurement, and service agreements. * Proven ability to manage ...

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Showing results 41-60

All JobsContract Msat Process Engineer JobsContract Msat Process Engineer Jobs in Raleigh, NC

Contract Msat Process Engineer information

See Raleigh, NC salary details

$48.1K

$89.4K

$138.5K

How much do contract msat process engineer jobs pay per year?

As of Aug 23, 2026, the average yearly pay for contract msat process engineer in Raleigh, NC is $89,449.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $100,100.00 per year, depending on experience, location, and employer.

What is a Contract MSAT Process Engineer?

A Contract MSAT (Manufacturing Science and Technology) Process Engineer is a professional who works on a temporary or project-based contract to support the development, optimization, and troubleshooting of manufacturing processes in industries such as pharmaceuticals or biotechnology. Their primary role is to ensure processes are efficient, compliant, and capable of producing high-quality products. They often collaborate with other departments, such as quality assurance and production, to implement process improvements, technology transfers, and scale-up activities. Contract positions typically mean the engineer is hired for a specific project or period rather than as a permanent employee.

What are the key skills and qualifications needed to thrive as a Contract MSAT Process Engineer?

To thrive as a Contract MSAT (Manufacturing Science and Technology) Process Engineer, you need a strong background in chemical or biochemical engineering, process optimization, and a relevant engineering degree. Familiarity with process simulation software (like Aspen or SuperPro), statistical analysis tools, and regulatory compliance standards such as cGMP is typically required. Excellent problem-solving, communication, and project management skills help drive cross-functional collaboration and process improvements. These competencies ensure efficient, compliant manufacturing processes and successful technology transfer in a highly regulated industry.

What are some common challenges faced by Contract MSAT Process Engineers during technology transfer projects?

Contract MSAT Process Engineers often encounter challenges such as aligning process specifications between sending and receiving sites, troubleshooting unexpected deviations during scale-up, and ensuring thorough documentation for regulatory compliance. Communication with cross-functional teams—including manufacturing, quality assurance, and R&D—is critical to anticipate and resolve issues quickly. Additionally, adapting to varying site capabilities and timelines requires strong project management and flexibility to deliver successful technology transfers.

What is the difference between Contract Msat Process Engineer vs Contract Chemical Process Engineer?

AspectContract Msat Process EngineerContract Chemical Process Engineer
CredentialsBachelor's in Chemical Engineering or related, certifications varyBachelor's in Chemical Engineering or related, certifications vary
Work EnvironmentManufacturing plants, chemical facilities, process optimizationRefineries, chemical plants, process design and improvement
Industry UsageOil & gas, petrochemicals, manufacturingChemical manufacturing, refining, pharmaceuticals

The Contract Msat Process Engineer and Contract Chemical Process Engineer roles share similar educational backgrounds and work environments, often within chemical and manufacturing industries. The main difference lies in their specific focus areas: Msat Process Engineers typically concentrate on process optimization and safety in manufacturing, while Chemical Process Engineers may focus more on process design and chemical reactions. Both roles require relevant engineering credentials and are vital in their respective sectors.

What are the most commonly searched types of Msat Process Engineer jobs in Raleigh, NC?

The most popular types of Msat Process Engineer jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Contract Msat Process Engineer jobs?

Cities near Raleigh, NC with the most Contract Msat Process Engineer job openings:

Contract Msat Process Engineer jobs near you
Infographic showing various Contract Msat Process Engineer job openings in Raleigh, NC as of August 2026, with employment types broken down into 11% Internship, 56% Full Time, and 33% Contract. Highlights an 89% In-person, and 11% Hybrid job distribution, with an average salary of $89,449 per year, or $43 per hour.

Associate Director, Process Development

AskBio

Durham, NC • On-site

Full-time

Posted 5 days ago

Job description

Opportunity for Secondment to AskBio
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
  • Speak with your direct manager to discuss your interest and alignment with your development goals.
  • Apply directly using the link provided in the posting.

We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary
The Associate Director, Process Development is a key position in the Cell Line & Process Development team, liaising between the development arms while serving as a subject matter expert (SME) for novel recombinant adeno-associated virus (rAAV) vector platform development. This position evaluates new cell lines in scale down models, develops end to end processes for production and purification with these novel cell substrates and recommends forward looking GMP activities based on development data.
This position is onsite at the BioPoint, RTP, NC facility, reporting to the VP of Cell Line & Process Development.
Job Responsibilities
  • Lead a team of Research Associates and Scientists responsible for developing viral vector manufacturing processes, scale-up, and internal technology transfer
  • Management of end to end platform development for novel rAAV producer cell lines applying statistical approaches for experimental execution and optimization
  • Oversee internal qualifications of GMP cell banks and critical raw materials in vector manufacturing processes
  • Partner with MSAT on life cycle management of clinical program manufacturing and optimization
  • Lead platform fit and/or development activities for portfolio programs, as needed
  • Identify and develop new technologies for increased productivity, recovery, product quality and/or improved cost of goods
  • Collaborate cross-functionally with other AskBio teams inside and outside of Technical Operations, including our partner CDMOs
  • Develop internal tech transfer documents and author/review CMC regulatory documents
  • Review and communicate experimental results both orally and in written reports/presentations to colleagues, senior management and at external partners and conferences
  • Identifes CapEx needs, develops corresponding budget and justification
  • Assists with the development of and adherence to department budgets
  • Identifies and executes against personnel plans, including hiring, training, and development in the pursuit of organizational objectives
  • Contributes to intellectual property strategies and manages staff to successful IP support
  • Author technical and development documents, including relevant sections in regulatory submissions
  • Mentors and develops team members by establishing a collaborative and growth minded culture that encourages personal and professional development
  • Present scientific data at internal forums and external conferences

Minimum Requirements
  • Master's Degree in a scientific or engineering discipline with a minimum of eight years of relevant work experience
  • Prior experience managing cross-functional teams of Research Associates, Scientists and/or Engineers
  • Prior experience with recombinant AAV and/or extensive experience in biologics employing relevant unit operations
  • Strong understanding of mammalian cell biology, engineering principles and how to interconnect them
  • Self-motivated leader with a track record of novel development of biologics demonstrated through publications, patents, posters and/or presentations
  • Functional expertise in design of experiments (DOEs) and Quality by Design (QbD) approaches
  • Excellent written and verbal communication skills
  • Good working knowledge of Microsoft Office suite (Word, Outlook, Excel) and statistical analysis software

Preferred Education, Experience and Skills
  • PhD in a scientific or engineering discipline
  • Cell line development for the production of AAV, antibodies or recombinant protein
  • Strong working knowledge of Benchling, QbD Vision and/or JMP

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at talent@askbio.com.

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