ZipRecruiter

Log In

1

Per Diem Analytical Method Development Jobs in Virginia

Concern Housing

Per Diem Counselor

Suffolk, VA · On-site

$20/hr

Great opportunity for professional development, for college students, or individuals looking for a ... Per Diem Counselors are required to have a High School Diploma or equivalent and some experience in ...

Valley Health

Physical Therapist - Per Diem

Front Royal, VA · On-site

$38.02 - $57.04/hr

The per diem therapist may be employed in any one of the rehab settings, is an active member of the ... development and process improvement initiatives. In addition, the employee maintains a working ...

Granules

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

Plan and execute method development, method validation and tech transfer activity for API, excipient, package components and Finish Product. * Oversees analytical techniques, interpretations of ...

Valley Health

Physical Therapist - Per Diem

Front Royal, VA · On-site

$38.02 - $57.04/hr

The per diem therapist may be employed in any one of the rehab settings, is an active member of the ... development and process improvement initiatives. In addition, the employee maintains a working ...

Chapters Health System

LPN Per Diem

Glen Allen, VA · On-site

$33/hr

Under RN supervision, the Per Diem - LPN is responsible for providing nursing interventions and ... developed by the Interdisciplinary Group (IDG). * Demonstrates clinical skills regarding ...

Chapters Health System

LPN Per Diem

Glen Allen, VA · On-site

$33/hr

Under RN supervision, the Per Diem - LPN is responsible for providing nursing interventions and ... developed by the Interdisciplinary Group (IDG). * Demonstrates clinical skills regarding ...

previous pagenext page

Showing results 21-40

All JobsPer Diem Analytical Method Development JobsPer Diem Analytical Method Development Jobs in Virginia

Per Diem Analytical Method Development information

What is the difference between Per Diem Analytical Method Development vs Per Diem Quality Control Analyst?

AspectPer Diem Analytical Method DevelopmentPer Diem Quality Control Analyst
Primary RoleDevelops and validates analytical methods for testing pharmaceuticalsPerforms routine testing and analysis of pharmaceutical products
Work EnvironmentLaboratory focused on method creation and validationLaboratory conducting routine quality testing
Required CredentialsBachelor's degree in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in quality testing

Per Diem Analytical Method Development specialists focus on creating and validating new analytical methods, while Per Diem Quality Control Analysts perform routine testing to ensure product quality. Both roles require similar educational backgrounds but differ in their primary responsibilities and work focus.

What are the most commonly searched types of Analytical Method Development jobs in Virginia?

The most popular types of Analytical Method Development jobs in Virginia are:

What cities in Virginia are hiring for Per Diem Analytical Method Development jobs?

Cities in Virginia with the most Per Diem Analytical Method Development job openings:

Per Diem Analytical Method Development jobs near you
Infographic showing various Per Diem Analytical Method Development job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Scientist III, Analytical R&D

Chantilly, VA • On-site

Granules Pharmaceuticals
See more jobs at Granules Pharmaceuticalsexternal

$85K - $95K/yr

Full-time

Re-posted 5 days ago

Job description

Job Type
Full-time
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.
Salary Description
$85,000 - $95,000/ Yearly

Apply