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Cmc In Biotech Jobs in Washington (NOW HIRING)

Director, Supplier Development

Gaithersburg, MD · On-site

$145K - $218K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... in the pharmaceutical or biotechnology industry. Specific experience in cell therapy highly desirable. * Experience in CMC, process development, and/or manufacturing required. Skills/Abilities:

Director, Supplier Development

Gaithersburg, MD · On-site

$145 - $218/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... in the pharmaceutical or biotechnology industry. Specific experience in cell therapy highly desirable. * Experience in CMC, process development, and/or manufacturing required. Skills/Abilities:

Director, Supplier Development

Gaithersburg, MD

$145K - $218K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... in the pharmaceutical or biotechnology industry. Specific experience in cell therapy highly desirable. * Experience in CMC, process development, and/or manufacturing required. Skills/Abilities:

Director, Supplier Development

Gaithersburg, MD · On-site

$145K - $218K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... in the pharmaceutical or biotechnology industry. Specific experience in cell therapy highly desirable. * Experience in CMC, process development, and/or manufacturing required. Skills/Abilities:

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... 100+ CMC programs , and 1,397 clinical trials across all phases. Our teams are involved in ...

Regulatory Affairs Director

Gaithersburg, MD

$162K - $213K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... CMC, Labeling and members of the submission and execution team. Mentor and provide performance ... biotechnology industry. * strong knowledge of global regulatory affairs in oncology, across ...

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... 100+ CMC programs , and 1,397 clinical trials across all phases. Our teams are involved in ...

Senior Accountant

Germantown, MD · On-site

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 ... 000+ CMC programs , and 1,000+ clinical trials across all phases. Our teams are involved in ...

Showing results 21-40

Cmc In Biotech information

What is the difference between Cmc In Biotech vs Formulation Scientist?

AspectCmc In BiotechFormulation Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Good Manufacturing Practice (GMP) knowledgeBachelor's or Master's in Pharmacy, Chemistry, or related field; GMP experience
Work EnvironmentLaboratories, manufacturing facilities, regulatory settingsLaboratories, R&D departments, manufacturing units
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract manufacturing organizationsPharmaceutical companies, biotech firms, contract labs

While both roles operate within the biotech and pharmaceutical industries, Cmc In Biotech focuses on Chemistry, Manufacturing, and Controls documentation and regulatory compliance, whereas Formulation Scientists primarily develop and optimize drug formulations. Cmc In Biotech professionals ensure regulatory submissions are complete, while Formulation Scientists work on creating effective drug delivery systems. Both roles often collaborate but serve distinct functions within the product development pipeline.

What is a CMC in biotech position?

A CMC (Chemistry, Manufacturing, and Controls) position in biotech involves overseeing the development, manufacturing, and quality control of biopharmaceutical products. Professionals in this role ensure that products meet regulatory standards and are produced consistently, often requiring knowledge of GMP (Good Manufacturing Practice) and regulatory guidelines.

What is a CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes involved in developing, producing, and ensuring the quality of a biopharmaceutical product. CMC professionals are responsible for regulatory compliance, process validation, and quality assurance to meet industry standards and facilitate product approval.

What is the CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes ensuring the quality, safety, and efficacy of a biotech product throughout development and production. Professionals in this field often work on regulatory submissions, quality assurance, and process validation to meet industry standards.

What are popular job titles related to Cmc In Biotech jobs in Washington?

For Cmc In Biotech jobs in Washington, the most frequently searched job titles are:

What cities in Washington are hiring for Cmc In Biotech jobs?

Cities in Washington with the most Cmc In Biotech job openings:

Infographic showing various Cmc In Biotech job openings in Washington as of June 2026, with employment types broken down into 75% Full Time, 15% Part Time, 5% Temporary, and 5% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution.

Associate Director, AS&T Lifecycle Management (Biological Method Expert)

BioNTech SE

Gaithersburg, MD • On-site

$146K - $234K/yr

Full-time

Re-posted 15 days ago


Job description

Associate Director, AS&T Lifecycle Management (Biological Method Expert)
Gaithersburg, US | full time | Unlimited | Job ID: 11546
About the Role:
As the Associate Director AS&T Lifecycle Management, you will be making a meaningful contribution to the ongoing product development and regulatory submission (BLA/MAA) of our Protein-based therapeutic pipeline as part of our Analytical Sciences & Technology (AS&T) department. In this role, you will be the main point of contact for specific methods within your area of expertise. You will ensure that the analytical methods comply with GMP standards and provide accurate, precise, and reliable results.
Your Contribution:
• Provide technical analytical expertise for analytical activities of the Gaithersburg antibody laboratory, and for late-stage and commercial projects across a global network
• Responsible for the design and performance of method validations and transfers as well as method lifecycle activities (e.g. exchange of critical reagents, method performance and laboratory investigations); potential hands-on work in the laboratory required
• Participate in strategic and technical discussions within projects cross-functionally with CMC team members and external partners
• Evaluation and review of technical and regulatory submission documents in a timely manner for the approval and market launch of development products
• Act as the Analytical SME by providing expert knowledge for regulatory filings, as well as contributing expertise to questions from health authorities and responses to regulatory submissions
A Good Match:
• An advanced university degree in Biology, Chemistry, Pharmacy, Biotechnology, or a related field with 10+ years in a regulated environment in the pharmaceutical industry
• Comprehensive expertise in chromatographic, spectroscopic, electrophoretic, immunoassay and molecular biology techniques for the analysis of mAbs/ADCs
• Hands-on experience with assay development, design and performance of method validations, as well as data analysis and statistical evaluation
• Strong background in CMC activities for late-stage development and commercial biological products
• In-depth knowledge of ICH guidelines, GMP regulations, and industry best practices
• Proven experience with regulatory filings for biologicals (IND/IMPD, BLA/MAA) and interactions with health authorities
• Experience in working in intercultural, cross-functional, and global teams
• Structured way of working, ability to understand and break down complex challenges and plan associated timelines and interdependencies
• Highly motivated and willingness to work in a fast-paced and fast-evolving environment
Preferred Qualifications:
Experience managing method validation and transfer activities across external partners.
Demonstrated ability to lead and support QC quality events and root cause investigations.
Your benefits and remuneration:
Expected Pay Range: $146,300/year to $234,100/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
Inspired? Join our team of pioneers and bright, open minds. From our founders to our scientists to our business professionals, we think out-the-box, believe in ourselves, work agile and stand accountable.
Together, we usher in a new era of immunotherapies and work on realizing our vision.
Do you have any questions?
Please contact Yushen Chang (Talent Acquisition) or jobs@biontech.de with reference to the job ID.
BioNTech, our story.
At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.
BioNTech does not tolerate discrimination, favoritism, or harassment based on gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important - it's a match!
Inspired? Become part of #TeamBioNTech.
BioNTech, the story
At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.
BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!
BioNTech - As unique as you
www.biontech.com