ZipRecruiter

Log In

1

Pharma Packaging Jobs in Reston, VA (NOW HIRING)

Granules

Scientist III, Analytical R&D

Chantilly, VA · On-site

$85K - $95K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule ...

Emmes

Study Start-Up Associate II

Rockville, MD · Remote

$34.25 - $46.75/hr

Works with team members on preparation of regulatory submission packages. * Tracks and follow up on ... Master's Degree MS, MPH, PharmD (Preferred) * 1 to 3 years working within pharma and/or CRO ...

Granules

Quality Control Manager

Chantilly, VA · On-site

$100K - $120K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule ...

Granules

Trainee Engineer

Chantilly, VA · On-site

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule ...

Granules Pharmaceuticals

Trainee Engineer

Chantilly, VA · On-site

$23 - $25/hr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule ...

previous page

Showing results 41-60

All JobsPharma Packaging JobsPharma Packaging Jobs in Reston, VA

Pharma Packaging information

See Reston, VA salary details

$13

$19

$28

How much do pharma packaging jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for pharma packaging in Reston, VA is $19.61, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $20.77 per hour, depending on experience, location, and employer.

What are some typical challenges faced in a pharma packaging role and how are they addressed?

In a Pharma Packaging role, maintaining strict compliance with regulatory standards and ensuring product integrity are common challenges. Team members must consistently monitor packaging lines for accuracy, prevent contamination, and document every step to meet Good Manufacturing Practice (GMP) requirements. Effective communication with quality assurance and production teams is essential to quickly resolve issues and minimize downtime. Ongoing training and adherence to standard operating procedures help address these challenges and maintain high-quality outcomes.

What is the difference between Pharma Packaging vs Pharma Quality Control?

AspectPharma PackagingPharma Quality Control
Required CredentialsHigh school diploma or technical training, certifications in packaging processesDegree in pharmacy, chemistry, or related field; certifications in quality assurance
Work EnvironmentManufacturing facilities, packaging linesLaboratories, testing facilities
Industry UsageEnsures proper packaging of pharmaceutical productsEnsures products meet quality standards through testing

Pharma Packaging focuses on the physical packaging of medicines, ensuring they are correctly labeled and sealed. Pharma Quality Control involves testing and inspecting products to meet safety and efficacy standards. Both roles are essential in pharmaceutical manufacturing but serve different functions within the industry.

What is pharma packaging?

Pharma packaging refers to the process and materials used to encase pharmaceutical products, such as tablets, capsules, liquids, and medical devices, to protect them from contamination, damage, and tampering. It ensures the safety, stability, and efficacy of medications throughout their shelf life and during transportation. Pharma packaging also includes labeling and regulatory information to help ensure that drugs are used safely by healthcare professionals and patients.

What are the key skills and qualifications needed to thrive in pharma packaging?

To excel in Pharma Packaging, you need a strong understanding of Good Manufacturing Practices (GMP), attention to detail, and a high school diploma or relevant technical certification. Familiarity with packaging machinery, labeling systems, and quality control tools is typically required. Strong teamwork, reliability, and problem-solving skills help individuals stand out in this role. These competencies ensure packaging compliance, product safety, and efficient operations in the highly regulated pharmaceutical industry.

What does a pharmaceutical packaging technician do?

A pharmaceutical packaging technician is responsible for assembling, labeling, and packaging medications and medical products according to strict quality and safety standards. They operate packaging machinery, inspect products for defects, and ensure compliance with regulatory requirements, often working in cleanroom environments. Attention to detail and knowledge of Good Manufacturing Practices (GMP) are essential for this role.
Pharma Packaging jobs near you
Infographic showing various Pharma Packaging job openings in Reston, VA as of August 2026, with employment types broken down into 78% Full Time, 17% Part Time, 1% Temporary, 2% Contract, and 2% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $40,780 per year, or $19.6 per hour.

Scientist III, Analytical R&D

Granules

Chantilly, VA • On-site

$85K - $95K/yr

Full-time

Re-posted 3 days ago

Job description

Description:


Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.


Job Duties & Responsibilities


Plan and execute method development, method validation and tech transfer activity for API, excipient, package components and Finish Product.

  • Oversees analytical techniques, interpretations of analytical data, problem solving and troubleshooting as required for Analytical R&D activities.
  • Prepare and review SOPs, protocols, reports, to support laboratory GMP function in compliance with FDA, ICH and other regulatory guidance.
  • Plan, review and implement additional studies (e.g., cleaning validation, Photostability, any in-use studies, Multimedia dissolution, shipping study, etc.)
  • Plan and design of experiments toward answering CMC deficiencies responses.
  • Perform Investigations (Out of trend, out of specification and laboratory deviations) as per SOP.
  • Conforms to all training requirements, including company required and regulatory requirements
  • Manages the AR&D function in the laboratory to ensure cGMP compliance.
  • Other duties related to departmental activities may be assigned by the management based on the requirement.
  • Provide regular timely reports, interpret analytical data and present results to the manager AR&D and Head as needed.


Management Responsibility


  • Reviews staff's performance regularly and develop team members to continually enhance both individual and overall work team performance.
  • Take an active role in identifying training needs, challenge and develop both direct and indirect reports in their positions for future opportunities.


Reports to


Manager to Analytical R&D.


Knowledge & Skills


  • Knowledge of API, excipient and finish product in generic pharmaceuticals.
  • Hands-on experience with drug substance and drug product analytical techniques such as HPLC, GC, KF, MS, dissolution, spectroscopy, and particle size.
  • Functional understanding of small molecule analytical development and associated regulatory and quality requirements.
  • In-depth understanding of GMPs and applicable CMC, analytical and manufacturing regulatory guidance.
  • Excellent verbal and written communication skills.
  • Excellent problem solving and interpersonal skills.


Requirements:

Experience & Education


  • Master's degree in Analytical Chemistry or Chemistry or related field with 5+ years OR PhD with 3+ years of experience
  • Experience small molecule solid oral dosage analytical development is required


Physical Requirements/Working Environment


  • Must be able to stand for long periods of time (up to 12-hour shifts), maneuver at least 40 pounds, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE.
  • Vision - ability to see details at close range (within a few feet of the observer).


Disclaimer


The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.



We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.