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Pharmaceutical Manufacturing Jobs in Reston, VA (NOW HIRING)

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

Must have a Bachelor's degree in Biochemistry, Chemistry, or Biotechnology plus 2 years experience in Quality Control within a Pharmaceutical Manufacturing company. Skills Requirements: Working ...

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

Must have a Bachelor's degree in Biochemistry, Chemistry, or Biotechnology plus 2 years experience in Quality Control within a Pharmaceutical Manufacturing company. Skills Requirements: Working ...

Requirements: * A background in cGMP compliance and DEA compliance within the pharmaceutical manufacturing industry is required. * Experience in writing and maintaining cGMP documentation.

... pharmaceutical manufacturing industry. · Writing and maintaining cGMP documentation. · Analyze data/information and resolve complex issues. · Verbal and written communication skills. · Work and ...

Showing results 21-40

Pharmaceutical Manufacturing information

See Reston, VA salary details

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How much do pharmaceutical manufacturing jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for pharmaceutical manufacturing in Reston, VA is $28.22, according to ZipRecruiter salary data. Most workers in this role earn between $23.99 and $33.03 per hour, depending on experience, location, and employer.

What is a pharmaceutical manufacturing job?

A Pharmaceutical Manufacturing job involves the production of medications, including their formulation, testing, packaging, and quality control. Workers in this field ensure compliance with regulatory standards, such as Good Manufacturing Practices (GMP), to guarantee product safety and efficacy. Roles may vary from machine operators and technicians to quality assurance specialists and process engineers. The job requires attention to detail, adherence to protocols, and an understanding of regulatory guidelines. Pharmaceutical manufacturers play a crucial role in delivering safe and effective medications to patients worldwide.

What are the typical daily responsibilities in a pharmaceutical manufacturing role?

In a Pharmaceutical Manufacturing role, your daily responsibilities usually include operating and monitoring production equipment, documenting manufacturing processes, and following strict safety and compliance protocols. You'll work closely with quality control teams to ensure all products meet regulatory standards, and may participate in troubleshooting and correcting production issues as they arise. Additionally, collaboration with engineers, technicians, and supervisors is common to optimize efficiency and uphold high-quality standards. These tasks help ensure the safe and reliable production of pharmaceutical products that meet both company and industry requirements.

What are the key skills and qualifications needed to thrive in a pharmaceutical manufacturing position?

To thrive in Pharmaceutical Manufacturing, you need a solid understanding of chemistry, biology, quality control, and regulatory compliance, often supported by a degree in life sciences or engineering. Familiarity with Good Manufacturing Practices (GMP), batch record software, and automated production equipment is crucial. Attention to detail, strong teamwork, and effective communication are standout soft skills for this role. These competencies are essential for maintaining product quality, ensuring regulatory adherence, and operating efficiently within a highly regulated and collaborative environment.

What does pharmaceutical manufacturing do?

Pharmaceutical manufacturing involves producing medications and vaccines in controlled environments, following strict quality and safety standards. It includes processes such as formulation, compounding, packaging, and quality control, often requiring knowledge of Good Manufacturing Practices (GMP) and specialized equipment. Workers in this field ensure that products meet regulatory requirements before reaching consumers.

What types of jobs are there in the pharmaceutical manufacturing industry?

Pharmaceutical manufacturing offers a variety of roles including production operators, quality control analysts, process engineers, formulation scientists, and packaging technicians. These jobs often require knowledge of Good Manufacturing Practices (GMP), attention to detail, and familiarity with manufacturing equipment and laboratory tools. Positions can range from entry-level to specialized technical and supervisory roles.

What are popular job titles related to Pharmaceutical Manufacturing jobs in Reston, VA?

For Pharmaceutical Manufacturing jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Manufacturing jobs in Reston, VA look for?

The top searched job categories for Pharmaceutical Manufacturing jobs in Reston, VA are:

What cities near Reston, VA are hiring for Pharmaceutical Manufacturing jobs?

Cities near Reston, VA with the most Pharmaceutical Manufacturing job openings:

Infographic showing various Pharmaceutical Manufacturing job openings in Reston, VA as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 4% Contract, and 2% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $58,688 per year, or $28.2 per hour.

Sr. Manager, External Manufacturing

Vanda Pharmaceuticals, Inc.

Washington, DC • On-site

$100 - $130/hr

Other

Medical, Retirement, PTO

Re-posted 16 days ago


Job description

Headquarters
Vanda Pharmaceuticals HQ
2200 Pennsylvania Avenue NW
Suite 300E
Washington, DC 20037, USA

  • Serve as the single point of accountability for assigned CMOs supporting commercial product manufacturing and packaging operations.
  • Ensure on-time, in-full (OTIF) delivery of commercial supply, meeting demand forecasts and inventory targets.
  • Own production planning alignment with Supply Chain, including capacity planning, campaign scheduling, and inventory optimization.
  • Proactively identify supply risks and lead mitigation strategies to ensure uninterrupted commercial supply
External CMO Management & Governance
  • Lead day-to-day operational oversight of CMOs, including production performance, issue resolution, and escalation management.
  • Establish and maintain robust governance processes (KPIs, business reviews, scorecards, and continuous improvement plans).
  • Drive vendor performance management, including quality, cost, delivery, and reliability metrics.
  • Partner with Procurement on contracting, scope definition, and cost optimization initiatives.
Technical & CMC Leadership
  • Provide technical oversight of commercial manufacturing processes, ensuring consistent product quality and performance.
  • Support and oversee technology transfers, process validation, scale‑up, and lifecycle management at external sites.
  • Lead or contribute to complex investigations, root cause analyses, and implementation of CAPAs.
  • Champion process robustness and continuous improvement initiatives across CMOs.
Quality & Compliance
  • Ensure all manufacturing activities comply with cGMP, regulatory filings, and quality agreements.
  • Collaborate closely with Quality Assurance on deviations, change controls, CAPAs, and audit readiness.
  • Support health authority inspections and ensure effective response to regulatory observations (if applicable).
  • Maintain compliance of technical documentation and manufacturing records.
Cross-Functional Integration
  • Partner with Supply Chain, Quality, Regulatory, Technical Development, and Commercial teams to align manufacturing operations with business priorities.
  • Ensure seamless communication of manufacturing performance, risks, and supply outlook to leadership.
  • Support launch readiness and ongoing lifecycle management for commercial products.
Regulatory Support
  • Contribute to CMC sections of regulatory submissions (NDA/ANDA variations, annual reports, supplements).
  • Ensure manufacturing processes and changes are aligned with global regulatory requirements.
Position Requirements Minimum Qualifications
  • Bachelor’s degree in Chemical Engineering, Pharmacy, Chemistry, or related discipline.
  • 7+ years of experience in pharmaceutical manufacturing, technical operations, or CMC.
  • Demonstrated experience managing external CMOs for commercial drug product and/or packaging operations.
  • Strong knowledge of cGMP regulations, commercial manufacturing operations, and tech transfer and process validation.
  • Proven ability to manage cross‑functional teams and external partners.
Preferred Qualifications
  • Advanced degree (MS, PhD, MBA).
  • Experience with commercial small‑molecule products (solid oral dosage and/or sterile).
  • Experience supporting regulatory filings and health authority inspections.
  • Strong track record in commercial supply chain management and vendor governance.
  • Experience in lifecycle management and post‑approval changes.
  • Proven success managing complex supply chains in a matrixed environment.
  • Strong ownership mindset for commercial supply reliability
  • Excellent vendor and stakeholder management skills
  • Ability to operate in a fast‑paced, matrixed environment
  • Strategic thinking with strong execution discipline
  • Effective problem‑solving and decision‑making under pressure

Must be able to perform the essential functions of the position, with or without reasonable accommodation; however, reasonable accommodations will be provided for qualified individuals with disabilities unless doing so would impose undue hardship.

The total compensation package for this position will also include incentive compensation and benefits such as health insurance, unlimited paid time off, parental leave, a 401k matching program, and other benefits to its employees.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, gender identity, sexual orientation, protected veteran status, or any other characteristic protected by law.

If you reside in a state or locality with enacted pay transparency laws, you are entitled to request and receive additional details regarding compensation and benefits. For assistance, please contact us at 202-524-8238 between 8:00 AM and 5:30 PM ET, Monday through Friday.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

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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