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Msat In Pharma Jobs (NOW HIRING)

Cross-Functional Collaboration - partners with Manufacturing and MSAT/Engineering on facility ... in cGMP pharma/biotech or sterile medical device manufacturing, including environmental/utility ...

$150 - $200/hr

... pharma, and emerging modalities. * Conduct deep competitive analysis of lab-scale tools and ... and MSAT groups to uncover unmet needs in early-stage workflows. * Identify whitespace ...

$22 - $29/hr

... MSAT/Engineering, QA/QC, EHS) to maintain product quality and patient safety. This role exists to ... in cGMP pharma/biotech or sterile medical device manufacturing, including environmental/utility ...

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How much do msat in pharma jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for msat in pharma in the United States is $71.16, according to ZipRecruiter salary data. Most workers in this role earn between $53.12 and $79.09 per hour, depending on experience, location, and employer.

What is the difference between Msat In Pharma vs Clinical Research Associate?

AspectMsat In PharmaClinical Research Associate
Required CredentialsBachelor's degree, often with certifications in clinical trials or pharmaceutical sciencesBachelor's degree, often with certifications in clinical research or Good Clinical Practice (GCP)
Work EnvironmentPharmaceutical companies, biotech firms, or contract research organizations (CROs)Clinical trial sites, hospitals, or research organizations
Employer & Industry UsagePrimarily in pharmaceutical and biotech industriesIn clinical trial management and monitoring

Msat In Pharma and Clinical Research Associate roles share similar educational backgrounds and certifications, often working within the pharmaceutical industry. While Msat In Pharma focuses on supporting clinical trial processes within pharmaceutical companies, Clinical Research Associates primarily monitor and manage clinical trial sites. Both roles are essential in drug development, but their work environments and specific responsibilities differ slightly.

What does Msat in pharma do?

Msat in pharma typically refers to a Medical Science Associate, a role responsible for supporting medical and scientific communication, conducting clinical research, and ensuring compliance with industry regulations. They often collaborate with healthcare professionals, provide product information, and may assist in training or educational activities within pharmaceutical companies.
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Infographic showing various Msat In Pharma job openings in the United States as of September 2026, with employment types broken down into 5% Internship, 4% As Needed, 83% Full Time, 3% Part Time, 4% Contract, and 1% Nights. Highlights an 78% Physical, 3% Hybrid, and 19% Remote job distribution, with an average salary of $148,012 per year, or $71.2 per hour.

Robotics Technology Deployment Steward (Drug Substance)

South San Francisco, CA • On-site

Roche
10K+ employees

$18 - $24.75/hr

Full-time

Posted 16 days ago


Key responsibilities

  • Support the deployment of standardized robotics and automation solutions across global manufacturing sites.

  • Lead cross-functional teams to design, execute, and evaluate proof-of-concept projects for robotics technologies.

  • Manage the end-to-end deployment lifecycle, including post-CAPEX industrialization, system integration, and operational handover.


Roche rating

9.3

Company rating: 9.3 out of 10

Based on 23 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical


Job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Roche's demanding and changing Small Molecules, Bio, and Cell & Gene Therapy product portfolio requires shaping the manufacturing network of the future, driving global investments across different production sites.

As an integral part of Pharma Technical Operations (PT), PT Global MSAT, Engineering and Sustainability (PTT) plays a key role in leading seamless industrialization and thorough technical management by integrating SHE, proactive maintenance, facility fitness, performance optimization, and scalable manufacturing technologies across the network. Product and process robustness, efficiency, and reliability are key performance indicators that PTT owns and drives through continuous improvement.

Within PTT, our Global Manufacturing Science and Technology (gMSAT) departments drive the front-line implementation of advanced capabilities to modernize physical operations across the Drug Substance (DS), Drug Product (DP), and Device, Packaging & Distribution (DDP) networks.

The Technology Deployment Groups (TDGs) within the gMSAT departments are the ultimate strategic connectors in our technology standardization framework. They coordinate the collection and assessment of both network-wide operational "pains" and emerging local innovations, bridging the gap between local site realities and globally endorsed network standards.


The Opportunity

As a vital member within the Drug Substance Technology Deployment Group, the Robotics Technology Deployment Steward serves as the primary execution engine bridging central strategy with site-level manufacturing operations. Working in close partnership with the Robotics Technology Strategy Lead, this role supports technology scouting, translates high-level strategy into value-driven proofs-of-concept (PoCs), and leads the tactical roll-out of standardized robotics and automation solutions to directly address operational pain points across our global production sites.

  • Site Pain Point Resolution & Technology Scouting: Act as the Drug Substance liaison for manufacturing sites, identifying operational bottlenecks, evaluating local challenges through a global network lens, and actively support the scouting for emerging robotics/automation solutions to drive standardized resolution.

  • Strategic Roadmap Co-Creation: Partner closely with the Technology Strategy Lead to drive and shape the global/network robotics roadmap, leading hands-on operational execution, provide technical expertise, and consolidate/represent site feasibility perspectives.

  • Proof of Concept (PoC) Execution: Lead cross-functional execution teams (across MSAT, Engineering, Quality, IT/OT, and Operations) to design, execute, and evaluate rapid, ROI-driven PoCs, providing data-backed recommendations to scale, pivot, or stop technologies based on business value.

  • Lead the end-to-end deployment lifecycle: Drive post-CAPEX industrialization plans, oversee cross-functional IT/OT system integration (e.g., SCADA, MES, digital twins), and manage the operational handover by preparing site integration packages (URS, CQV/CSV) to ensure a successful transition to local site operations.

Who you are

You are a pragmatic innovator with deep technical knowhow and hands-on expertise in deploying robotics and automation within complex regulated manufacturing environments, driven to solve critical site operational challenges through scalable technology.

  • BSc, MSc or PhD in Robotics Engineering, Mechatronics, Electrical/Mechanical Engineering, Automation Engineering, Chemical/Biochemical Engineering, or a related technical discipline. Bonus/Preferred: Additional education or certifications in Business Administration (e.g., MBA), Change Management, or Systems Engineering with 6+ years of relevant hands-on industrial experience in robotics integration, complex automation deployment, or manufacturing engineering within pharmaceutical/biotech or other highly regulated industries (e.g., semiconductor, aerospace), with direct involvement in major Capital Expenditure (CAPEX) project lifecycles and CQV exposure.

  • Proven ability to lead cross-functional technical teams and drive multi-site project deployments without direct hierarchical authority.

  • Practical understanding of IT/OT integration layers (SCADA/MES) and basic data/coding literacy (e.g., Python, SQL) to evaluate system performance metrics and drive data-informed decisions. Data processing capabilities is a plus.

  • Excellent project management, problem-solving with a track record of project completion.

  • Demonstrated experience deploying targeted automation solutions in the Drug Substance domain: e.g., AMRs for heavy mobile logistics, automated fluid transfer, robotic aseptic sampling, or automated single-use system (SUS) manipulation.

Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!

Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.Who we are

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let's build a healthier future, together.

Roche is an Equal Opportunity Employer.


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