ZipRecruiter

Log In

1

Cmc Writing Jobs in Texas (NOW HIRING)

Leidos

Project Manager (NASA CMC)

Webster, TX

$73K - $132K/yr

... Contract (CMC). In this position the employee will manage projects for the development and ... Experience working with multi-discipline teams and customers and both strong oral and written ...

New

Leidos

Project Manager (NASA CMC)

Webster, TX · On-site

$73K - $132K/yr

... Contract (CMC). In this position the employee will manage projects for the development and ... Experience working with multi-discipline teams and customers and both strong oral and written ...

New

Commercial Metals Company

Project Manager

Buda, TX · On-site

At CMC, it's the people inside our recycling centers, fabrication plants, manufacturing facilities ... Write and review RFIs for cost impact * Maintain project reports for management and customers

Commercial Metals Company

Project Manager

Buda, TX · On-site

At CMC, it's the people inside our recycling centers, fabrication plants, manufacturing facilities ... Write and review RFIs for cost impact * Maintain project reports for management and customers

Commercial Metals Company

AI Intern- SIOP

Irving, TX

At CMC, it's the people inside our recycling centers, fabrication plants, manufacturing facilities ... Excellent written and verbal communication skills * Ability to learn quickly and work independently

Commercial Metals Company

Rebar Fabricator

Houston, TX · On-site

At CMC, it's the people inside our recycling centers, fabrication plants, manufacturing facilities ... Excellent communication skills, in both written and verbal form are necessary to be successful in ...

next page

Showing results 1-20

All JobsCmc Writing JobsCmc Writing Jobs in Texas

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 Texas?

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

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

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

What cities in Texas are hiring for Cmc Writing jobs?

Cities in Texas with the most Cmc Writing job openings:

Cmc Writing jobs near you
Infographic showing various Cmc Writing job openings in Texas as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 100% In-person job distribution.

Associate Director, Regulatory Affairs - CMC

Orano

Plano, TX • On-site

Full-time

Posted 25 days ago

Job description

Description
Orano Med Theranostics
Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.
The Associate Director, Regulatory Affairs - CMC will be responsible for leading the global regulatory CMC strategy for product development and registration, and for the preparation of CMC dossier in the expanding field of radiopharmaceuticals in the US and in EU.
This global role will join the regulatory team and will report directly to the Head of Regulatory Affairs. The person will work cross-functionally with the CMC team and the manufacturing sites to lead the regulatory CMC strategy and the preparation of regulatory CMC documentation and submissions in adherence to relevant regulatory requirements and company standards.
Key Responsibilities:
  • Leads the development and preparation of global (US and EU) CMC-related submission documents for the pipeline of radiopharmaceutical products. This includes authoring, review and consolidation to deliver high-quality documents. Working in close collaboration with the CMC team (Manufacturing, Quality, R&D process), the regulatory CMC lead will collect technical data from relevant partners to write regulatory CMC documents and support the overall project goals.
  • Develops robust global regulatory CMC strategies for the pipeline of radiopharmaceutical products. Identifies risks and proposes risk mitigation to enable successful regulatory submissions and approvals. Aligns within Regulatory Affairs to enable one regulatory voice.
  • The regulatory submissions include but are not limited to the M3/CMC section of INDs/CTAs (IMPD-Q), DMF/ASMF, briefing documents, response to queries, Orphan Drug Applications, and annual reports.
  • Manages regulatory CMC agency interactions and meetings.
  • Meets current regulatory standards and achieves timely submissions, to enable approval on the first review cycle. Effectively interprets and applies regulatory CMC guidance. Provides recommendations and solutions to cross-functional teams and key stakeholders.
  • Works with the Regulatory Operations vendor to coordinate publishing and submission for CMC dossiers (eCTD)
  • Leads or contributes to the development of internal processes to improve the regulatory and CMC ways of working.
  • Remains current on CMC regulatory intelligence.

Requirements
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.
Minimum Qualifications:
  • Bachelor's degree in a scientific discipline. Advanced degree (MS, PharmD or PhD) is a plus.
  • A minimum of 8 years Regulatory CMC experience and/or CMC technical writing experience in a pharmaceutical or biotechnology environment including injectables.

Required Skills and Competencies:
  • Demonstrated hands-on experience in pharmaceutical development, registration in the US and/or EU, and interaction with health authorities. Demonstrated experience in preparing regulatory submissions, including IND/CTA, NDA/MAA, DMF/ASMF, briefing documents, and response to agency questions.
  • Technical knowledge in small molecules with experience in translating to a regulatory document. Knowledge of radiopharmaceuticals and innovative platforms is a plus.
  • Knowledge of relevant global CMC regulations and guidelines (ICH, US, EU)
  • Experience within a GMP environment with a firm understanding of industry regulations and best practices
  • Ability to understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements and strategy.
  • Excellent verbal and written communication skills. Able to defend the regulatory CMC position while maintaining positive professional relationships
  • Proactive, able to work independently and collaboratively in a fast-paced emerging field
  • Analytical thinker with good problem-solving skills and the capacity to adapt to a field with relatively few guidelines available.
  • Excellent planning and organization skills including the ability to support multiple projects.
  • Proficiency with Microsoft Office.
  • Travel requirements: Up to 10% travel

Apply