ZipRecruiter

Log In

1

Syner G Biopharma Group Jobs in Reston, VA (NOW HIRING)

Fladger Associates

Senior Scientist

Gaithersburg, MD · On-site

$98K - $135K/yr

The group plays an integral part in the design and development of patient centric drug products ... Knowledge of protein biochemistry and degradation mechanisms, biopharmaceutical manufacturing ...

Astrazeneca

Regulatory Affairs Associate

Gaithersburg, MD · On-site

$85K - $127K/yr

Provide support across the group for assigned non-drug project roles & responsibilities e.g. act as ... Relevant experience in science from biopharmaceutical industry, or other relevant experience

AstraZeneca

Regulatory Affairs Manager

Gaithersburg, MD · On-site

$109K - $163K/yr

Review of documents (e.g. response documents, study protocols, PSRs, etc.). * Analysis of ... Provide coaching, mentoring and knowledge sharing within the RAM skill group. * Contribute to ...

Astrazeneca

Regulatory Affairs Manager

Gaithersburg, MD · On-site

$109K - $163K/yr

Review of documents (e.g. response documents, study protocols, PSRs, etc.). * Analysis of ... Provide coaching, mentoring and knowledge sharing within the RAM skill group. * Contribute to ...

AstraZeneca

Regulatory Affairs Manager

Gaithersburg, MD · On-site

$109K - $163K/yr

Review of documents (e.g. response documents, study protocols, PSRs, etc.). * Analysis of ... Provide coaching, mentoring and knowledge sharing within the RAM skill group. * Contribute to ...

Emmes

Senior Medical Officer

Rockville, MD · On-site +1

Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical ... biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and ...

next page

Showing results 1-20

All JobsSyner G Biopharma Group JobsSyner G Biopharma Group Jobs in Reston, VA

Syner G Biopharma Group information

See Reston, VA salary details

$36.4K

$76.6K

$119.6K

How much do syner g biopharma group jobs pay per year?

As of Aug 18, 2026, the average yearly pay for syner g biopharma group in Reston, VA is $76,639.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,400.00 and $88,400.00 per year, depending on experience, location, and employer.

What is the difference between Syner G Biopharma Group vs Clinical Research Associate?

AspectSyner G Biopharma GroupClinical Research Associate
Required credentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree, often with clinical research certifications
Work environmentBiopharmaceutical company, research labs, clinical trial sitesClinical trial sites, hospitals, research organizations
Employer and industry usageBiotech and pharmaceutical industry, research-focusedHealthcare, clinical research organizations, pharma companies

Syner G Biopharma Group primarily focuses on biopharmaceutical research and development, often involving laboratory work and clinical trials. Clinical Research Associates (CRAs) typically oversee clinical trial progress at various sites, ensuring compliance and data integrity. While both roles require similar educational backgrounds and certifications, Syner G Biopharma Group roles are more research and lab-oriented, whereas CRAs are more field-based, monitoring clinical trials across locations.

What are popular job titles related to Syner G Biopharma Group jobs in Reston, VA?

For Syner G Biopharma Group jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Syner G Biopharma Group jobs in Reston, VA look for?

The top searched job categories for Syner G Biopharma Group jobs in Reston, VA are:

What cities near Reston, VA are hiring for Syner G Biopharma Group jobs?

Cities near Reston, VA with the most Syner G Biopharma Group job openings:

Syner G Biopharma Group jobs near you
Infographic showing various Syner G Biopharma Group job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $76,639 per year, or $36.8 per hour.

Senior Scientist

Fladger Associates

Gaithersburg, MD • On-site

$98K - $135K/yr

Contractor

Re-posted 8 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Senior Scientist in the Gaithersburg, MD area.
  • The Late-Stage Formulation Sciences Group is responsible for development of intended commercial formulations to advance the late-stage biologics portfolio, and the life cycle management of commercialized products.
  • The group plays an integral part in the design and development of patient centric drug products.
  • This is a Scientific position, and the incumbent will be responsible for late-stage formulation development of biologic products.
  • Will be involved in the design and execution of formulation risk assessments and characterization studies, and development formulation control strategies for Drug Substance and Drug Product.
  • Ensure robustness of intended commercial formulations, suitability for intended use of container closure/packaging systems, and in-use compatibility with clinical administration components.
  • Expected to exercise technical discretion and scientific rigor in experimental protocol design, data analysis, and results interpretation.
  • Other responsibilities include authoring of marketing applications and provision of support to regulatory responses to approval.
  • Develop new strategies and approaches to advance late-stage formulation development and deliver scientific and operational objectives.

Experience:

  • BS, MS, or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, applied Sciences
  • Knowledge of protein biochemistry and degradation mechanisms, biopharmaceutical manufacturing processes, combination drug products, and/or biophysical analytical methods is required.
  • Hands-on experience with high-performance size exclusion chromatography (HPSEC), particle characterization and sizing (e.g., light obscuration), and aggregate characterization methods are strongly preferred.
  • Experience with formulation and biopharmaceutical development, characterization, control strategy, quality risk management, and/or CMC regulatory guidance and filings is preferred.
  • Skills leading, planning, and executing complex projects on tight timelines are important.