What Pharmaceutical Industries Jobs are in the United States?

Dormont Manufacturing Co is looking for a Project Engineer III to lead engineering projects, ensuring that pharmaceutical products are developed and manufactured effectively. With a minimum of 7 years' experience in GMP and project management, you will oversee project planning and execution in a dynamic environment. This position requires strong analytical skills, excellent communication, and the ability to collaborate with various teams. A Bachelor’s degree in Engineering or related field is essential for success in this role. #J-18808-Ljbffr

About Varda

Low Earth orbit is open for business. Varda is accelerating the development of commercial space infrastructure, from in-orbit pharmaceutical processing to reliable and economical reentry capsules.

From life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind.

Our team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital.

Varda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested. Varda also has offices in Washington, DC and Huntsville, AL.

Join Varda, and work to create a bustling in-space ecosystem.

As a Principal Fluid Systems Engineer on Varda's Payload team, you will define and lead the development of first-of-its-kind electromechanical fluid handling hardware that manufactures pharmaceuticals in microgravity, endures hypersonic reentry, and returns to Earth for material extraction. Your payloads will precisely meter, mix, filter, transport, and thermally control pharmaceutical materials in compact spacecraft-compatible hardware. You’ll shape the architecture and technical direction for pharmaceutical payloads—guiding project teams from requirements synthesis through development, on-orbit operation, recovery, and iteration for future missions.

You’ll collaborate closely with pharmaceutical scientists, process engineers, internal leadership, and spacecraft subsystem teams to translate mission objectives into qualified hardware that flies in months, not years. This role is ideal for engineers who combine deep mechanical and fluid systems expertise with the cross‑functional breadth to define foundational in-space pharmaceutical manufacturing infrastructure.

• Define requirements, architecture, and development plans for pharmaceutical manufacturing payloads
• Establish fluid system design standards for component selection and qualification, sealing, contamination control, thermal control, and verification/validation
• Lead project teams to develop precision fluid systems incorporating valves, pumps, pistons, manifolds, tubing, fittings, seals, filters, sensors, and thermal control systems
• Drive system-level analyses, trade studies, and risk reduction using a variety of tools (hand calcs, Python/MATLAB models, FEA, etc. as needed)
• Lead build and test campaigns for prototypes and flight hardware to characterize performance and reliability
• Synthesize cross-functional inputs from business development, pharmaceutical science, process engineering, and spacecraft subsystem teams to develop requirements for new pharmaceutical payloads
• Develop standards for subsystem requirements, ICDs, verification plans, test reports, and recovery procedures
• Represent Varda in technical discussions with internal leadership, external partners, customers, and government stakeholders
• Lead continuous improvement and incorporation of lessons learned
• Mentor senior and entry-level engineers and shape best practices

• BS/BEng in Mechanical, Aerospace, Mechatronics, Biomedical, Chemical, or related engineering discipline
• 7+ years of experience designing, integrating, testing, and troubleshooting electromechanical hardware
• Deep mechanical and fluid systems expertise with breadth in at least two adjacent disciplines such as avionics, software, thermal, optics, test, precision instrumentation, etc.
• Track record leading project teams through full-cycle electromechanical space flight hardware development
• Extensive experience with valves, pumps, pistons, tubing, manifolds, fittings, seals, filters, sensors, metering hardware, thermal-control hardware, and/or compact fluidic assemblies
• Excellent communication skills with customer, executive, and cross-disciplinary technical audiences

• 3+ years of cross‑functional project leadership experience
• Prior full-cycle technical leadership of precision fluid-handling hardware for relevant applications
  • In Space: ECLSS, low‑thrust propulsion, astronaut suits, spacecraft thermal control, etc.
  • On Earth: semiconductor process equipment, biotech process equipment, analytical instruments, medical devices, etc.
• Extensive experience planning and executing aerospace environmental testing (vibration, TVAC, EMI/EMC)
• Familiarity with microgravity fluid behavior, capillary‑driven flows, gas/liquid separation, two‑phase flow, cGMP principles, cleanroom practices, or regulated hardware environments

• Salary range: $170,000 - $220,000 per year
• This role is on‑site in El Segundo, CA
• Leveling and base salary is determined by job‑related skills, education level, experience level, and job performance
• You will be eligible for incentives in the form of stock options and/or long‑term cash awards

Varda, like all employers, must ensure that its employees working in the United States are lawfully authorized to work in the U.S. Additionally, our employees are exposed to and have access to certain export‑controlled items. At present, some of our technology to which employees have access requires a license to be exported to individuals other than "U.S. Persons" as defined in U.S. export regulations. Because our employees are provided access to export‑controlled items, our current policy is to only hire "U.S. persons" who are permitted to have access to our technology without an export license.

"U.S. person" means: U.S. citizen, U.S. lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3) (i.e., individual admitted to the U.S. as a refugee or granted asylum in the U.S.).

Learn more about the ITAR here.

• Exciting team of professionals at the top of their field working by your side
• Equity in a fully funded space startup with potential for significant growth (interns excluded)
• 401(k) matching (interns excluded)
• Unlimited PTO (interns excluded)
• Health insurance, including Vision and Dental
• Lunch and snacks provided on site every day. Dinners provided twice a week.
• Maternity / Paternity leave (interns excluded)

Varda Space Industries is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Candidates and employees are always evaluated based on merit, qualifications, and performance. We will never discriminate on the basis of race, color, gender, national origin, ethnicity, veteran status, disability status, age, sexual orientation, gender identity, martial status, mental or physical disability, or any other legally protected status.

Varda Space Industries, Inc. participates in the U.S. Department of Homeland Security E-Verify program. The E-Verify program is an Internet‑based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Learn more about the E-Verify program.

This role involves supporting the GxP Facility Operations/Engineering department at pharmaceutical GxP sites as part of the Reliability Engineering team. The responsibilities include ensuring equipment/system reliability through best practices and continuous improvement initiatives, managing documentation, and collaborating with various stakeholders to optimize asset management, calibration, preventative maintenance, and spare parts management. The ideal candidate should have an aptitude for mechanical and electrical systems, a minimum engineering degree or equivalent experience, and familiarity with GMP, ISO, GAMP, ANSI standards. Experience with CMMS and developing metrics/KPIs is also required. Preferred skills include GMP experience.

• Position: Reliability Engineer - Direct Hire
• Start Date: ASAP, end of May
• Pay Rate: $50-$70/hr
• Seniority Level: Mid-Senior level
• Employment Type: Full-time
• Job Function: Engineering and Production
• Industry: Facilities Services

Our client, a renowned pharmaceutical manufacturer, is seeking an experienced Senior Quality Assurance Manager to lead their Quality Assurance department in Colorado Springs, Colorado, US . This role offers a hybrid work model, blending essential on-site responsibilities with the flexibility of remote work. You will be responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS) to ensure compliance with all relevant regulatory standards, including FDA, GMP, and ISO. This leadership position requires a strong understanding of pharmaceutical manufacturing processes and a commitment to upholding the highest standards of quality and compliance. You will manage a team of QA professionals, drive continuous improvement initiatives, and serve as a key liaison with regulatory agencies. Our client is dedicated to producing high-quality pharmaceutical products and seeks a leader who shares this commitment.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with cGMP, FDA, and international regulations.
• Oversee all QA activities, including batch record review and release, change control, deviation management, CAPA, and internal/external audits.
• Lead and mentor the Quality Assurance team, fostering a culture of compliance and continuous improvement.
• Ensure that all manufacturing processes and products meet established quality standards and specifications.
• Manage regulatory inspections and audits, ensuring a positive outcome and addressing any findings promptly.
• Conduct risk assessments and implement mitigation strategies to address potential quality issues.
• Review and approve validation protocols and reports for equipment, processes, and analytical methods.
• Collaborate with Production, R&D, and other departments to ensure quality is integrated throughout the product lifecycle.
• Develop and deliver quality training programs for relevant personnel.
• Stay updated on current GMP regulations, industry trends, and best practices in pharmaceutical quality assurance.

• Bachelor's degree in Science (e.g., Chemistry, Biology, Pharmacy) or Engineering. Advanced degree preferred.
• A minimum of 7-10 years of progressive experience in Quality Assurance within the pharmaceutical or related regulated industry.
• Extensive knowledge of GMP regulations, ICH guidelines, and FDA/EMA requirements.
• Proven experience in managing a QA team and implementing QMS across a manufacturing environment.
• Strong understanding of pharmaceutical manufacturing processes, validation, and analytical testing.
• Excellent leadership, communication, and interpersonal skills.
• Demonstrated experience in handling regulatory inspections and successful audit outcomes.
• Strong analytical and problem-solving abilities.
• Proficiency in quality management software and tools.
• Ability to work effectively in a hybrid work environment, balancing on-site and remote responsibilities.

• Competitive base salary and executive bonus structure.
• Comprehensive medical, dental, and vision insurance.
• Generous 401(k) plan with company match.
• Paid time off, including vacation, sick days, and company holidays.
• Opportunities for professional development and advanced training.
• Wellness programs and on-site fitness facilities.
• Life and disability insurance.
• Relocation assistance may be available for qualified candidates.
• Retirement planning services.
• A culture that values quality, integrity, and innovation.

Exela Pharma Sciences LLC is looking for a Reliability Engineer to establish a data-driven reliability program for critical pharmaceutical utility systems in Lenoir, NC. The role involves improving equipment reliability and optimizing maintenance strategies while utilizing SAP EAM.

The ideal candidate will have a Bachelor’s degree in Engineering and at least 5 years of experience in a GMP-regulated manufacturing environment. Strong expertise in utility systems and reliability methodologies is essential.