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Pharmaceutical Manufacturing Jobs in Reston, VA (NOW HIRING)

S. in Engineering discipline (Chemical /Biochemical strongly preferred) * 7 to 10 years' experience in cGMP, 21CFR Part 820, 21CFR Part 210 and 211, and/or Pharmaceutical manufacturing. Specific ...

Calibration Technician

Rockville, MD · On-site

$22.50 - $30.50/hr

Rockville, MD Contract Duration: 3 Years Position Overview We are seeking a Calibration Technician to support calibration and validation activities within a GMP-regulated pharmaceutical manufacturing ...

... or pharmaceutical manufacturing environments. · Strong experience with DCS, PLC, SCADA, ISA-88 batch systems, process historians, MES/LIMS integration, and industrial networking. · Hands-on ...

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are ...

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are ...

Pharmaceutical Manufacturing Facilities * Federal Healthcare Projects Day to Day: * Manage healthcare construction projects from start to finish * Walk projects with Superintendents and field teams

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Pharmaceutical Manufacturing information

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$19

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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.

Health Care & Policy / FDA - Associate Attorney (Washington, DC)

Talantage

Washington, DC • On-site

Other

Posted 19 days ago


Job description

Job Title: Health Care & Policy / FDA - Associate
Practice Area: Health Care & Life Sciences
Employment Type: Full-time
Talantage is seeking an immediate opening for a Health Care Associate to join our client's respected Health Care practice.
Key Responsibilities
  • Advise clients on complex regulatory compliance issues relating to drugs and medical devices.
  • Provide guidance on matters involving current Good Manufacturing Practices (CGMP).
  • Support clients with compliance strategies, risk assessments, and regulatory submissions.
  • Collaborate with internal teams and external stakeholders to navigate FDA-related challenges.
Qualifications
  • J.D. degree with 3-4 years of relevant experience in health care, life sciences, or related regulatory work.
  • Active license to practice in DC required.
  • Strong background in drug and medical device regulatory compliance; CGMP experience is highly desirable.
  • Prior industry experience in pharmaceutical manufacturing or a scientific background (analytical chemistry, chemical engineering, microbiology) preferred.
  • Experience at the Food and Drug Administration (FDA) is a plus.
  • Excellent academic credentials, writing skills, and interpersonal abilities are required.
Why Join?
  • Be part of a leading health care regulatory team tackling cutting-edge compliance issues.
  • Work with a diverse client base in the pharmaceutical, biotechnology, and medical device sectors.
  • Opportunity to grow your expertise at the intersection of law, science, and public health.
Talantage, LLC is committed to presenting candidates that contribute to an organizations culture of inclusivity and its commitment to diversity in the workplace are demonstrated through our recruitment practices. We are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, gender, gender identity, sexual orientation, marital status, national origin, citizenship status, disability, age, or veteran status. Our equal opportunity employment efforts comply with all applicable U.S. state and federal laws governing non-discrimination in employment.