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Cmc Writing Jobs in Virginia (NOW HIRING)

Granules

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

In-depth understanding of GMPs and applicable CMC, analytical and manufacturing regulatory guidance. * Excellent verbal and written communication skills. * Excellent problem solving and interpersonal ...

Option Care Health

Nutrition Care Coordinator

Richmond, VA · On-site

$17.02 - $28.38/hr

Communicates with CMC Pump Champion and pharmacy/warehouse teams on enteral pump needs, problems ... Excellent oral and written communication skills. Excellent customer service skills. * Flexible and ...

New

Always Family HomeCare

RN Care Manager

Vienna, VA · On-site

$40 - $55/hr

Visit clients in their homes to conduct initial assessments and re-assessments, write client care ... Certification as CMC, CCM, or other Care Management certification, or the requisite experience to ...

Associa

Assistant Community Manager

Annandale, VA · On-site

$28 - $35/hr

CMC, an Associa company, is hiring an Assistant Community Manager for its condominium community in ... Excellent communication skills (written and oral) and conflict resolution techniques. * Effective ...

Associa

Recreation Attendant (Part time)

Haymarket, VA · On-site

$15 - $16/hr

CMC, an Associa company, is hiring a part time Facilities Recreation Attendant for its large-scale ... Excellent communication skills, written and spoken. * High level of customer service skills.

Noblis

Principal Regulatory Scientist

Reston, VA · On-site

... CMC, and regulatory information and translate complex findings into clear, defensible decision support for multidisciplinary program teams and government stakeholders. * Strong technical writing ...

Associa

Recreation & Operations Manager

Haymarket, VA · On-site

$60K - $70K/yr

CMC, an Associa company, is hiring a Recreation & Operations Manager for its large-scale HOA ... Prepare detailed bid comparisons and written recommendations for management, committees, and the ...

Enlyte

Medical Field Case Manager

Sterling, VA · On-site

$76K - $95K/yr

Proficient grammar, sentence structure, and written communication skills. * Certifications ... CMAC, CMC) preferred. * Travel: Must have reliable transportation and be able to travel to and ...

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Showing results 21-40

All JobsCmc Writing JobsCmc Writing Jobs in Virginia

Cmc Writing information

What is the difference between Cmc Writing vs Medical Writing?

AspectCmc WritingMedical Writing
Required CredentialsBachelor's degree in life sciences, chemistry, or related field; often certifications in pharmaceutical writingDegree in life sciences, healthcare, or related; certifications like AMWA or DIA often preferred
Work EnvironmentPharmaceutical companies, biotech firms, contract research organizations (CROs)Pharmaceutical companies, medical communication agencies, CROs
Industry UsageFocuses on Chemistry, Manufacturing, and Controls documentation for drug approvalEncompasses clinical study reports, regulatory documents, and scientific publications

In summary, Cmc Writing specializes in regulatory documentation related to drug manufacturing and chemistry, while Medical Writing covers a broader range of clinical and scientific communication. Both roles require similar credentials and often work within the pharmaceutical industry, but they focus on different aspects of drug development and documentation.

What are typical Cmc Writing job responsibilities?

Cmc Writing jobs typically involve creating, editing, and reviewing scientific or technical documentation related to chemistry, manufacturing, and control processes. Responsibilities include ensuring compliance with regulatory standards, preparing detailed reports, and collaborating with cross-functional teams. Strong writing skills, knowledge of industry regulations, and attention to detail are essential for this role.

What is a Cmc Writing?

Cmc Writing typically refers to writing related to Chemistry, Manufacturing, and Controls (CMC) in the pharmaceutical industry, involving documentation for drug development and regulatory submissions. It requires strong technical writing skills, attention to detail, and knowledge of regulatory standards. Professionals in this field often work with scientific data, validation protocols, and compliance documentation.

What are popular job titles related to Cmc Writing jobs in Virginia?

For Cmc Writing jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Cmc Writing jobs in Virginia look for?

The top searched job categories for Cmc Writing jobs in Virginia are:

What cities in Virginia are hiring for Cmc Writing jobs?

Cities in Virginia with the most Cmc Writing job openings:

Cmc Writing jobs near you
Infographic showing various Cmc Writing job openings in Virginia as of August 2026, with employment types broken down into 91% Full Time, and 9% Contract. Highlights an 100% In-person job distribution.

Scientist III, Analytical R&D

Granules Pharmaceuticals

Chantilly, VA • On-site

$85K - $95K/yr

Full-time

Re-posted 17 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

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