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Remote Gmp Manufacturing Jobs (NOW HIRING)

Lonza

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... S. growth investment project, ensuring successful start-up and transition into routine GMP ...

Jade Biosciences

The role provides QA oversight of contract manufacturers (CMOs) and service providers supporting ... This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and ...

Sail Biomedicines

Sr. Engineer, Drug Product

Cambridge, MA · On-site +1

$130K - $150K/yr

Provide person-in-plant or remote technical support Process Modeling & Data Analysis * Develop and ... Experience in process development, manufacturing sciences, technical operations, or GMP ...

Lonza

Director, Automation

Walkersville, MD · On-site +1

$203K - $237K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... GMP manufacturing from day one. * Lead the automation workstream for an assigned U.S. growth ...

Strive Pharmacy

GMP Systems Administrator

Alachua, FL · On-site +1

Remote (U.S.) - Candidates must be able to travel to our Alachua, FL facility as needed. Preference ... This role sits at the intersection of IT, OT and pharmaceutical manufacturing compliance, ensuring ...

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... Ensure manufacturing operations are aligned with GMP requirements, quality systems, safety ...

Lonza

Director, Operations

Walkersville, MD · On-site +1

$198K - $232K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... Ensure manufacturing readiness and GMP compliance through commissioning, qualification, validation ...

Lonza

Director, MSAT

Walkersville, MD · On-site +1

$205K - $239K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... Strong knowledge of GMP manufacturing operations, regulatory requirements, commissioning ...

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How much do remote gmp manufacturing jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for remote gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are some common challenges of working in a remote GMP manufacturing role, and how can they be addressed?

Working remotely in GMP (Good Manufacturing Practice) manufacturing presents unique challenges, such as ensuring strict compliance with regulatory standards without being physically present on-site. Communication with on-site teams is crucial to maintain oversight and address any deviations or quality concerns promptly. Leveraging digital tools, clear documentation, and regular virtual meetings can help bridge the gap. It’s also important to stay updated on the latest regulatory changes and maintain strong collaboration with quality assurance, production, and validation teams to ensure all processes are followed accurately.

What is the difference between Remote Gmp Manufacturing vs Remote Quality Assurance?

AspectRemote Gmp ManufacturingRemote Quality Assurance
CredentialsGMP certifications, technical manufacturing experienceGMP certifications, quality control certifications
Work EnvironmentManufacturing facilities, labs, or remote production oversightRemote review, audits, documentation, and compliance checks
Industry UsagePharmaceutical, biotech, and medical device manufacturingPharmaceutical, biotech, and medical device industries
Common Search IntentManufacturing processes, production oversightQuality compliance, audits, documentation

Remote Gmp Manufacturing focuses on overseeing and managing manufacturing processes remotely, ensuring production meets GMP standards. Remote Quality Assurance emphasizes maintaining quality compliance through remote audits, reviews, and documentation. Both roles require GMP certifications but differ in daily tasks and focus areas within the industry.

What are the key skills and qualifications needed to thrive as a remote GMP manufacturing professional?

To thrive as a Remote GMP Manufacturing professional, you need in-depth knowledge of Good Manufacturing Practices (GMP), quality control, and regulatory compliance, typically supported by a degree in life sciences or engineering. Familiarity with digital manufacturing systems, batch record management software, and possibly certifications like Six Sigma or GMP training is essential. Strong attention to detail, problem-solving skills, and effective remote communication set outstanding candidates apart. These skills ensure the integrity of product quality and regulatory compliance, even in a remote or decentralized work environment.

What is remote GMP manufacturing?

Remote GMP manufacturing refers to the oversight, management, or operation of Good Manufacturing Practice (GMP) compliant production processes from a location outside the actual manufacturing facility. This can involve remote monitoring of production data, quality control, and compliance activities using digital tools and secure communication platforms. The goal is to maintain high standards of product quality and regulatory compliance, even when staff or consultants are not physically present onsite. This approach has become more common due to advancements in technology and the increased need for flexibility in the pharmaceutical and biotechnology industries.
More about Remote Gmp Manufacturing jobs
What cities are hiring for Remote Gmp Manufacturing jobs? Cities with the most Remote Gmp Manufacturing job openings:
What are the most commonly searched types of Gmp Manufacturing jobs? The most popular types of Gmp Manufacturing jobs are:
What states have the most Remote Gmp Manufacturing jobs? States with the most job openings for Remote Gmp Manufacturing jobs include:
What job categories do people searching Remote Gmp Manufacturing jobs look for? The top searched job categories for Remote Gmp Manufacturing jobs are:
Remote Gmp Manufacturing jobs near you
Infographic showing various Remote Gmp Manufacturing job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 3% In-person, and 97% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Director, Manufacturing

Lonza

Walkersville, MD • On-site, Remote

$198K - $232K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

Director, Manufacturing
Location: This position is currently remote. A future transition to an on-site location on the U.S. East-Coast/Mid-West is anticipated as the project progresses, with an expected timeline in 2027. This is a full-time role with a Monday-Friday schedule from 8:00 a.m. to 5:00 p.m.
What you will get:
The full-time base annual salary for this position is expected to range between $198,900 to $232,050. In addition, below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus.
  • Medical, dental and vision insurance.
  • 401(k) matching plan.
  • Life insurance, as well as short-term and long-term disability insurance.
  • Employee assistance programs.
  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What will you do:
The Director, Manufacturing - US Growth Investment Projects is responsible for developing and executing the operational readiness strategy for an assigned U.S. growth investment project supporting bioconjugate drug substance manufacturing. This role serves as the primary Operations representative throughout facility design, construction, commissioning, qualification, validation, start-up, and operational handover, ensuring the new facility is GMP-compliant, inspection-ready, and capable of supporting clinical and commercial manufacturing from day one.
Working closely with the End-to-End Program Lead, Global Engineering, Quality, MSAT, Manufacturing, Automation, EHS, HR, and Finance, the Director will ensure operational requirements are embedded throughout the project lifecycle while building the future manufacturing organization and operating model.
  • Lead operational readiness activities for an assigned U.S. growth investment project, ensuring successful start-up and transition into routine GMP manufacturing operations
  • Develop and execute the operations readiness roadmap, including organizational design, workforce planning, training strategy, process readiness, validation support, and operational handover
  • Define the future manufacturing organization, including staffing plans, shift structures, organizational interfaces, governance models, and operational ownership
  • Serve as the primary Operations representative for facility and process design reviews, ensuring manufacturing requirements are incorporated into equipment, automation, process flow, and facility decisions
  • Partner with Engineering, Quality, MSAT, Automation, and EHS to ensure operational requirements are appropriately integrated throughout project execution
  • Establish processes and systems that ensure GMP compliance, operational excellence, inspection readiness, and long-term manufacturing reliability
  • Lead operational planning and readiness activities associated with technology transfers, customer onboarding, process implementation, and commercial launch activities
  • Identify, assess, and mitigate operational, technical, organizational, and project risks associated with staffing, training, equipment readiness, start-up execution, and manufacturing performance
  • Build, develop, and lead a high-performing manufacturing organization while fostering a culture of accountability, safety, quality, and continuous improvement
  • Provide operational readiness updates, risk assessments, mitigation strategies, and recommendations to project governance teams and senior leadership

What we are looking for:
  • Master's degree in engineering, Biotechnology, Life Sciences, Pharmaceutical Sciences, or a related discipline preferred; bachelor's degree with significant relevant experience will also be considered
  • 12+ years of leadership experience within pharmaceutical, biotechnology, biologics, or bioconjugate manufacturing environments
  • Demonstrated experience leading manufacturing operations within a CDMO environment, including customer-facing interactions, technology transfers, operational planning, and support of multiple client programs
  • Significant experience supporting or leading bioconjugate drug substance manufacturing operations, including scale-up, validation, technology transfer, start-up, and commercial manufacturing
  • Proven experience supporting major capital projects, facility expansions, greenfield or brownfield investments, and manufacturing facility start-ups
  • Strong knowledge of GMP manufacturing operations, regulatory requirements, process validation, commissioning, qualification, operational readiness, and inspection preparedness
  • Demonstrated success leading large, cross-functional teams and influencing stakeholders across Operations, MSAT, Quality, Engineering, Automation, EHS, Supply Chain, HR, Finance, and Project Management
  • Experience building manufacturing organizations, developing talent, and preparing teams for successful operational launch and long-term site performance
  • Strong understanding of customer requirements within a CDMO business model, including program execution, relationship management, and delivery against customer commitments
  • Strategic thinker with the ability to translate business objectives into scalable operational solutions
  • Excellent communication and executive presentation skills, with experience presenting to senior leaders, governance bodies, customers, and external stakeholders
  • Demonstrated capability to identify and mitigate operational, technical, compliance, and project execution risks
  • Knowledge of Lean Manufacturing, Six Sigma, automation systems, digital manufacturing platforms, and data integrity principles preferred
  • Ability to operate effectively in a fast-paced project environment with evolving priorities and multiple stakeholders
  • Ability and willingness to transition to an East Coast or Midwest U.S. site location as project needs evolve
  • Willingness and ability to travel domestically and internationally up to approximately 25-30% of the time

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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