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Contract Manufacturing Jobs in Washington (NOW HIRING)

Electra Aero, Inc.

Manufacturing Engineer

Manassas, VA · On-site

$6.5K/mo

The Role Electra.aero is seeking a Manufacturing Engineer to join on a fixed 8-month contract term, supporting the development and industrialization of next-generation electric aircraft. This is a ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Contract Compensation: $18.00 - $25.00 hourly Overview The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Contract Compensation: $18.00 - $25.00 hourly Overview The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Contract Compensation: $18.00 - $25.00 hourly Responsibilities * Participate in hands-on production support in the manufacturing of material for clinical trials in a GMP environment by conducting ...

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Contract Manufacturing information

What are the key skills and qualifications needed to thrive in contract manufacturing?

Excelling in contract manufacturing requires a solid understanding of production processes, supply chain management, and quality control, often backed by a degree in engineering, manufacturing, or business. Familiarity with ERP systems, manufacturing execution systems (MES), and ISO or GMP certifications is highly valued. Strong negotiation skills, attention to detail, and effective communication are essential soft skills. These competencies help ensure efficient production, seamless client collaboration, and adherence to quality and regulatory standards.

What does a contract manufacturing do?

A contract manufacturing professional oversees the production of goods on behalf of a client company, ensuring products meet quality standards and specifications. They coordinate with suppliers, manage manufacturing processes, and often work with tools like ERP systems to streamline operations.

What is contract manufacturing?

A Contract Manufacturing job involves managing the production of goods through third-party manufacturers. Professionals in this role oversee vendor relationships, ensure quality control, negotiate contracts, and coordinate supply chain logistics. They work closely with suppliers to meet cost, production, and timeline requirements. This position is common in industries like pharmaceuticals, electronics, and consumer goods.

What types of companies or industries typically hire for contract manufacturing roles?

Contract manufacturing roles are in demand across a wide variety of industries, including pharmaceuticals, consumer goods, electronics, automotive, and food and beverage. Job seekers can expect to find opportunities with both specialized contract manufacturing organizations (CMOs) and large corporations that outsource aspects of their production processes. These positions often involve collaborating with diverse clients, managing production timelines, and ensuring adherence to high quality and regulatory standards. Working in this field can provide valuable exposure to multiple industries, offering strong potential for career advancement and skill development.

What are the most commonly searched types of Manufacturing jobs in Washington? The most popular types of Manufacturing jobs in Washington are:
What are popular job titles related to Contract Manufacturing jobs in Washington? For Contract Manufacturing jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Contract Manufacturing jobs in Washington look for? The top searched job categories for Contract Manufacturing jobs in Washington are:
What cities in Washington are hiring for Contract Manufacturing jobs? Cities in Washington with the most Contract Manufacturing job openings:
Contract Manufacturing jobs near you
Infographic showing various Contract Manufacturing job openings in Washington as of August 2026, with employment types broken down into 87% Full Time, 2% Temporary, 9% Contract, and 2% Nights. Highlights an 100% In-person job distribution.

Validation Engineer I

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
The Validation Engineer I supports activities within the Drug Delivery Sciences department related to process development, validation, and technology transfer. This role will develop, lead, and execute pre-validation studies and engineering activities. In addition, this role will partner with contract manufacturing organizations (CMOs) to support manufacturing scale up and operations readiness. Incumbents in this role will support in house formulation and process development, author sections of regulatory filing documents, and collaborate cross functionally to ensure timely delivery of clinical trial materials.
Essential Duties & Responsibilities:
  • Develops and conducts statistical analyses, including Design of Experiments (DOE) and Statistical Process Controls (SPC) to evaluate and improve manufacturing processes.
  • Leads pre-validation studies and engineering batches to identify and define critical process parameters of a process at Contract Manufacturing Organizations (CMO).
  • Write and review study protocols, technical reports, and validation documentation to ensure alignment with regulatory and quality standards.
  • Reviews and approves manufacturing batch records, protocols, and reports.
  • Supports process technology transfer to Contract Manufacturing Organization (CMO).
  • Assists with manufacturing scale-up manufacturing, process registration, and process validation activities at CMOs.
  • Recommends and implements equipment and manufacturing processes to ensure successful process technology transfer, process registration, and validation.
  • Writes and reviews of equipment qualification documents, Standard Operating Procedures (SOPs), and work instructions.
  • Collaborates cross functionally to support the manufacture of Clinical Trial Materials (CTM) and ensure the timely delivery to clinical programs.
  • Writes and reviews relevant quality sections of regulatory filing documents (IND, NDA, Briefing packages, IMPD, CTA, etc.).
  • Support early phase product and process development in collaboration with Drug Delivery Sciences teams.
  • Other duties as assigned.

Supervisory Responsibilities:
  • N/A.

Knowledge & Other Qualifications:
  • Bachelor's degree in engineering and a minimum of two years of relevant industry experience in manufacturing, process development, scale-up, technology transfer, or process validation.
  • Previous experience writing equipment validation protocols or technical writing.
  • Working knowledge of cGMP requirements related to Drug Product manufacturing processes.
  • Demonstrated ability to solve complex technical problems with the use of data.
  • Previous experience working with Statistical models and conducting statistical analyses a plus.
  • Strong written and verbal communication skills are required.
  • Proficiency with Microsoft office suite (Word, Excel, Outlook) required.

Other Characteristics:
  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability to have an innovative and dynamic approach to work.
  • A self-starter able to work independently but comfortable working in a team environment.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers and others.
  • Capable of performing other duties as assigned by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:
  • Sedentary work, when not working in the lab. Exerting up to 10 pounds of force occasionally and/or carry objects. Sedentary work involves sitting most of the time.
  • When in the lab, employees will be required to exert up to approximately 50 pounds of force occasionally and/or up to 30 pounds of force frequently, as well as exerting up to 10 pounds of force constantly to move objects, when working in the lab.
  • The employee is required to have close visual acuity to perform an activity such as preparing and analyzing data and figures; viewing a computer screen, iPad, or other electronic device; and extensive reading. The worker is also required to have the visual acuity to perform activities such as operating machines, and to perform mechanical or skilled trade tasks of a non-repetitive nature.
  • Will be required to work in a clean processing room environment occasionally and wear personal protective equipment to include but not limited to gloves, safety glasses or goggles, face shields, lab coats, ear plugs, half mask air purifying respirator, or powered air purifying respirator (PAPR) and Tyvek suits occasionally.
  • The employee is not substantially exposed to adverse environmental conditions on a regular basis. Employees may have to wear Tyvek suits when working in the lab, which can make conditions warmer, and more challenging. Employees will be required to work and exert force while wearing Tyvek suits.
  • Position may require prolonged sitting, prolonged standing, balancing, stooping, bending, kneeling, crouching, walking and pushing.
  • Travel will be project and phase dependent. Phase 2 or small-scale process technology transfers may require 20-40% of travel a month. Large-scale technology transfers, scale up, registration and validation may require 50-90% of travel a month.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $74,000 to $85,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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