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Biotech Pharmacist 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 ...

High School Diploma or BS and a minimum of three years of related experience in the biotech/pharmaceutical industry. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders ...

D. in Chemistry, Biotechnology, Biology, Biochemistry, Cell Biology, Bioengineering, Pharmaceutical Sciences, or a related scientific discipline. * Experience developing potency, functional, or ...

High School Diploma or BS and a minimum of three years of related experience in the biotech/pharmaceutical industry. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders ...

Bioassay Researcher

Silver Spring, MD · On-site

$85K - $141K/yr

D. in Chemistry, Biotechnology, Biology, Biochemistry, Cell Biology, Bioengineering, Pharmaceutical Sciences, or a related scientific discipline. * Experience developing potency, functional, or ...

Territory Rep - BioPharma

Alexandria, VA · On-site

$86K - $117K/yr

Pharmaceutical Sales Representative (Specialty to entry level both available) Pharmaceutical Sales Rep Opening Summary: We are seeking driven, capable, vivacious as well as positive sales account ...

Minimum 5-8 years of clinical data management experience in biotechnology, pharmaceutical, medical device, diagnostics, or companion diagnostic development. * Hands-on experience with CDISC standards ...

Requirements High School Diploma or equivalent with exposure to science and math coursework, and minimum three years of related biotech/pharmaceutical industry experience or Associate's degree in a ...

Internships in life sciences, food policy, biotechnology, pharmaceuticals, consulting, communications, public policy, commercial organizations, or startups. Bonus Points If You Have Familiarity with ...

Requirements High School Diploma or equivalent with exposure to science and math coursework, and minimum three years of related biotech/pharmaceutical industry experience or Associate's degree in a ...

Bonus Points If You Have • Familiarity with pharmaceutical, biotechnology, medical device, diagnostics, food, or agriculture industries; • Experience with Salesforce, LinkedIn Sales Navigator ...

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Biotech Pharmacist information

See Reston, VA salary details

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How much do biotech pharmacist jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for biotech pharmacist in Reston, VA is $63.37, according to ZipRecruiter salary data. Most workers in this role earn between $58.27 and $70.00 per hour, depending on experience, location, and employer.

What is a biotech pharmacist?

A biotech pharmacist is a licensed pharmacist who specializes in the use, management, and dispensing of biotechnological medications, such as biologics and biosimilars. These professionals often work with complex drugs derived from living organisms, which are used to treat conditions like cancer, autoimmune diseases, and rare genetic disorders. Biotech pharmacists collaborate with healthcare teams to ensure safe administration, educate patients about these therapies, and monitor for side effects. Their role is crucial as biotechnology continues to transform the pharmaceutical landscape, requiring advanced knowledge in both pharmacy and biotechnology.

How does a biotech pharmacist typically collaborate with research and development teams in a pharmaceutical company?

A Biotech Pharmacist frequently works alongside research and development (R&D) teams to ensure the safe and effective integration of biotechnology products into clinical practice. This collaboration often involves reviewing clinical trial protocols, advising on drug formulation and delivery, and interpreting regulatory requirements for new biologic therapies. By bridging the gap between scientific research and patient care, Biotech Pharmacists help translate laboratory discoveries into viable treatment options, while also providing insights on manufacturing, quality assurance, and post-marketing surveillance. Effective communication and interdisciplinary teamwork are essential in this dynamic work environment.

What are the key skills and qualifications needed to thrive as a biotech pharmacist, and why are they important?

To thrive as a Biotech Pharmacist, you need a strong background in pharmacy, pharmacology, and biotechnology, typically supported by a PharmD degree and relevant licensure. Familiarity with laboratory information management systems (LIMS), pharmacovigilance databases, and certifications such as Board Certified Pharmacotherapy Specialist (BCPS) are highly beneficial. Attention to detail, problem-solving skills, and effective communication enable success in interdisciplinary teams and regulatory environments. These competencies ensure safe, innovative medication management and compliance with complex biotech industry standards.

How much does a biotech pharmacist make?

A biotech pharmacist typically earns between $100,000 and $140,000 annually, depending on experience, location, and employer. They often work in pharmaceutical or biotech companies, requiring knowledge of drug development and regulatory compliance.

What cities near Reston, VA are hiring for Biotech Pharmacist jobs?

Cities near Reston, VA with the most Biotech Pharmacist job openings:

Infographic showing various Biotech Pharmacist job openings in Reston, VA as of August 2026, with employment types broken down into 2% Internship, 2% As Needed, 70% Full Time, 23% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $131,814 per year, or $63.4 per hour.

Pharmaceutical Manufacturing Technician

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 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 Pharmaceutical Manufacturing Technician supports drug product development and manufacturing activities by operating, setting up, cleaning, and maintaining pharmaceutical processing equipment and manufacturing areas. This position is responsible for executing batch records, preparing processing suites for R&D and GMP operations, maintaining laboratory and manufacturing supplies, documenting activities accurately, and supporting scientific studies and manufacturing campaigns under the direction of scientists and manufacturing leadership.
Essential Duties & Responsibilities:
  • Set up, operate, monitor and tear down pharmaceutical manufacturing processing equipment used in the drug product development and manufacturing activities.
  • Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations.
  • Execute manufacturing operations in accordance with approved batch records, standard operating procedures (SOPs), and current Good Manufacturing Practices (cGMP).
  • Perform equipment cleaning, room clearance, and room turnover activities to ensure readiness for manufacturing operations.
  • Assist with equipment troubleshooting maintenance activities in collaboration with engineering personnel, vendors, and equipment service providers.
  • Support technology transfer, scale-up and process development activities as assigned.
  • Execute batch records, logbooks, forms, and support manufacturing documentation accurately and in real time.
  • Record detailed observations during manufacturing development and experimental activities.
  • Report deviations, equipment issues, and operational concerns to management promptly.
  • Maintain cleanliness and organization of manufacturing suites, laboratories, equipment, and support areas.
  • Perform routine cleaning and sanitization activities according to approved procedures.
  • Maintain inventory of laboratory, manufacturing, and cleaning supplies.
  • Coordinate ordering and replenishment of materials and consumables as needed.
  • Collect, document and communicate experimental observations and results accurately.
  • Assist scientists with process development, formulation development, equipment evaluations and process characterization studies.
  • Follow all company safety procedures, environmental health and safety requirements and cGMP regulations.
  • Maintain a safe, compliant and inspection-ready work environment.
  • Participating in training programs and maintaining required qualifications for assigned responsibilities.

Supervisory Responsibilities:
  • N/A

Knowledge & Other Qualifications:
  • High School Diploma or equivalent 1+ Pharmaceutical GMP manufacturing, drug product development, laboratory operations packaging, or comparable experience.
  • Associate degree in Pharmaceutical Technology, Biotechnology, Chemistry, Biology, Engineering Technology or a related scientific field preferred.
  • Experience working in a cGMP environment is desirable.
  • Knowledge of GMPs and other commonly used concepts, practices, and procedures within the pharmaceutical industry preferred.
  • Knowledge of solid dosage form manufacturing including but not limited to encapsulation, manufacture of compressed tablets, fluid bed processing, high shear granulation, tablet coating, blending, etc., preferred.
  • Ability to follow written procedures, batch records, and scientific protocols.
  • Familiarity with pharmaceutical processing equipment and manufacturing operations.
  • Strong attention to detail and documentation practices.
  • Ability to identify and communicate processes, equipment, and quality concerns.
  • Strong organizational skills and time-management skills.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Basic troubleshooting and problem-solving abilities.
  • Proficiency with Microsoft Office applications and electronic documentation systems preferred.
  • Working knowledge of safety, health, and environment regulations, including the proper handling of chemicals, hazardous materials, waste disposal, and the use of personal protective equipment (PPE) Ability to write and adhere to internal written procedures.
  • Ability to work with hazardous waste and laboratory chemicals.

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:
  • When in the development labs or GMP suites, 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 exert 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; transcribing; 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 GMP processing room environment that requires wearing 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.
  • The employee is not substantially exposed to adverse environmental conditions on a regular basis. Employee may have to wear Tyvek suits when working in the development labs or GMP suites, which can make conditions warmer, and more challenging. Employee will be required to work and exert force while wearing Tyvek suits.

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 $48,000 to $55,000. 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.