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Pharmaceutical Manufacturing Jobs in Reston, VA (NOW HIRING)

Mintex Technology

Production Operator II

Chantilly, VA · On-site

$76K/yr

Pharmaceutical Manufacturing Benefits: * Competitive compensation * Health, Dental & Vision Insurance * 401(k) & Company Benefits * Training & Career Growth Opportunities * Stable pharmaceutical ...

Artius Solutions

Production Operator

Chantilly, VA · On-site

$47K - $70K/yr

Manufacturing Job Summary The Production Operator is responsible for performing pharmaceutical manufacturing activities in accordance with current Good Manufacturing Practices (cGMP), internal ...

Jedson Engineering Inc

Mechanical/HVAC Engineer

Reston, VA · On-site

$88K - $118K/yr

Mechanical Engineer (HVAC - Pharmaceutical Process Facilities) We are seeking a Registered Professional Mechanical Engineer with strong HVAC design experience in pharmaceutical drug manufacturing ...

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All JobsPharmaceutical Manufacturing JobsPharmaceutical Manufacturing Jobs in Reston, VA

Pharmaceutical Manufacturing information

See Reston, VA salary details

$19

$28

$41

How much do pharmaceutical manufacturing jobs pay per hour?

As of Jul 27, 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 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.

How do you get into pharmaceutical manufacturing?

To enter pharmaceutical manufacturing, candidates typically need a high school diploma or equivalent, with many roles requiring a bachelor's degree in pharmacy, chemistry, or a related field. Relevant skills include attention to detail, knowledge of Good Manufacturing Practices (GMP), and familiarity with manufacturing equipment; certifications like cGMP training can enhance job prospects.

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 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 use of specialized equipment. The role ensures that medicines are safe, effective, and meet regulatory requirements.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Manufacturing position, and why are they important?

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 is the highest paying pharmaceutical job?

In pharmaceutical manufacturing, senior roles such as Director of Manufacturing or Vice President of Production tend to be the highest paying, often earning six-figure salaries. These positions typically require extensive experience, leadership skills, and knowledge of regulatory compliance and process optimization.

What jobs are there in the pharmaceutical industry?

The pharmaceutical industry offers a variety of jobs including roles such as pharmaceutical manufacturing technician, quality control analyst, research scientist, regulatory affairs specialist, production supervisor, and packaging operator. These positions often require knowledge of Good Manufacturing Practices (GMP), attention to detail, and sometimes specialized certifications or degrees in pharmacy, chemistry, or related fields.
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:
Pharmaceutical Manufacturing jobs near you
Infographic showing various Pharmaceutical Manufacturing job openings in Reston, VA as of July 2026, with employment types broken down into 84% Full Time, 3% Part Time, 10% Contract, and 3% Nights. Highlights an 86% In-person, 7% Hybrid, and 7% Remote job distribution, with an average salary of $58,688 per year, or $28.2 per hour.

QA Associate - Pharmaceutical Manufacturing

Granules Pharmaceuticals

Manassas, VA • On-site

$55K - $65K/yr

Full-time

Posted 9 days ago

Job description

Job Type
Full-time
Description
Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules' packaging facility and front-end division for private label over the counter (OTC) products in the US. We offer OTC generics that meet the highest level of quality at an affordable cost. As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance. We are dedicated to excellence in manufacturing, quality, and customer service.
The QA associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing inspections, batch record review, and quality system functions in accordance with cGMP and related company SOP's, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.
Job Duties & Responsibilities
  • Manage and maintain company document control and archival systems (hardcopy and electronic) in compliance with internal procedures and policies as well as regulatory requirements.
  • Manage the routing, review, approval, distribution and archival of new and revised controlled documents.
  • Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
  • Archive and maintain hardcopy and electronic copies of batch records files, audit files, vendor files, product, label files and change history files.
  • Control and issuance of labeling components.
  • Manage all document control logbooks and spreadsheets.
  • Perform the release of finished product batches packaged.
  • Provide new hire training on GMP's, Safety, and Pharmacovigilance and maintain the training program documentation.
  • Ensure standard operating procedures are periodically reviewed for relevance and accuracy in compliance with company policies and procedures.
  • Collaborate with team members to ensure timely deliverables for documentation.
  • Ensuring all documents are up to date with respect to version control and issuance
  • Perform and support maintenance and closure activities of documents such as reports, protocols exceptions/deviations, CAPAs, change controls and complaints.
  • cGMP Compliance in Document Control.
  • Any other activity as assigned by the Supervisor

Requirements
Knowledge & Skills
  • cGMP compliance within the pharmaceutical manufacturing industry.
  • Writing and maintaining cGMP documentation.
  • Analyze data/information and resolve complex issues.
  • Verbal and written communication skills.
  • Work and communicate with cross-functional teams.
  • Multiple priorities and re-prioritize tasks.

Experience & Education
  • At least two (2) years' experience in a quality assurance role in a cGMP-regulated environment.
  • A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.)

Physical Requirements/Working Environment
  • While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
  • Specific vision abilities required by this job include close vision requirements due to computer work.
  • Ability to sit at a computer terminal for an extended period of time.
  • Light to moderate lifting up to 10-15 lbs. is required.
  • Ability to work in a confined area.

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
Salary Description
$55,000 - $65,000 per year

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