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At Cdmo Jobs in Florida (NOW HIRING)

Evergen

Sr. R&D Project Manager

Alachua, FL · On-site

$100K - $125K/yr

This rebranding reflects our strategic evolution as a leading CDMO in regenerative medicine and comes at the end of a significant year for the business, including the successful acquisitions of Cook ...

Evergen

Operations Engineer 2

Alachua, FL · On-site

$80K - $90K/yr

This rebranding reflects our strategic evolution as a leading CDMO in regenerative medicine and comes at the end of a significant year for the business, including the successful acquisitions of Cook ...

Evergen

Facilities Engineer 2

Alachua, FL · On-site

$80K - $95K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Evergen

Buyer 2

Alachua, FL · On-site

$65K - $75K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Evergen

Sr. Quality Engineer

Alachua, FL · On-site

$90K - $115K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Evergen

Operations Engineer 2

Alachua, FL · On-site

$75K - $95K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Evergen

Operations Manager

Alachua, FL · On-site

$100K - $120K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Jacobs Management Group

Packaging Engineer

Alachua, FL

$65K - $80K/yr

This role puts you at the center of operations, owning the design and development of packaging ... Work for a global CDMO with manufacturing facilities across the US, Europe, and New Zealand...real ...

Evergen

Operations Supervisor

Alachua, FL · On-site

$65K - $80K/yr

... organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is ...

Quotient Sciences

File Clerk - Per Diem

Miami, FL · On-site

$15.75 - $19/hr

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... To ensure data is stored safe in a manner that minimizes deterioration and prevent loss at all ...

Quotient Sciences Limited

File Clerk - Per Diem

Miami, FL · On-site

$15.75 - $19/hr

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... To ensure data is stored safe in a manner that minimizes deterioration and prevent loss at all ...

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All JobsAt Cdmo JobsAt Cdmo Jobs in Florida

At Cdmo information

What is the difference between At Cdmo vs Clinical Research Associate?

AspectAt CdmoClinical Research Associate
Required credentialsTypically requires a degree in life sciences, pharmacy, or related field; certifications varyRequires a degree in life sciences or healthcare; often requires GCP or ICH certifications
Work environmentContract manufacturing or development labs, regulatory compliance settingsClinical trial sites, hospitals, or research organizations
Employer and industry usagePharmaceutical, biotech, and contract manufacturing organizationsPharmaceutical companies, CROs, research institutions

While both roles involve the pharmaceutical industry, At Cdmo professionals focus on manufacturing and development processes within CDMOs, whereas Clinical Research Associates oversee clinical trial activities at research sites. The credentials and work environments overlap but serve different stages of drug development.

What are popular job titles related to At Cdmo jobs in Florida? For At Cdmo jobs in Florida, the most frequently searched job titles are:
What job categories do people searching At Cdmo jobs in Florida look for? The top searched job categories for At Cdmo jobs in Florida are:
At Cdmo jobs near you
Infographic showing various At Cdmo job openings in Florida as of July 2026, with employment types broken down into 17% As Needed, and 83% Full Time. Highlights an 100% In-person job distribution.

Associate Director/Director, CMC Analytical Development, Separation

Syncromune

Fort Lauderdale, FL • On-site, Remote

$165K - $200K/yr

Full-time

Re-posted 12 days ago

Job description

The Associate Director/Director of CMC Analytical Development will oversee the execution of the analytical strategy for drug substance and drug product development across all phases of clinical development and commercialization. This role is responsible for overseeing method development, validation, transfer, and lifecycle management to ensure compliance with regulatory requirements and alignment with company objectives.
Principal Duties and Responsibilities include the following:
  • Define and implement analytical development strategies to support CMC programs from early development through commercialization.
  • Provide technical leadership in analytical sciences, including chromatography, spectroscopy, and characterization techniques.
  • Guide analytical development activities at CDMO and CTL, including method development, optimization, transfer, validation, troubleshooting, and lifecycle management for GMP test methods for DS and DP.
  • Guide extended characterizations in support of comparability and regulatory applications.
  • Foster collaboration with cross-functional groups including Process Development, Quality, and Regulatory Affairs.
  • Author and review analytical sections of regulatory submissions (IND, IMPD, NDA, BLA).
  • Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities.
  • Drive continuous improvement and innovation in analytical technologies and processes.
Supervisory Responsibilities:
  • Indirect Reports: supervise CDMO, CTL, and external resources (such as consultants)
Qualification Requirements:
Education:
  • Ph.D. or M.S. degree in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
Experience:
  • Must have 8+ years of pharmaceutical or biotechnology industry experience specializing in analytical development.
  • Must have working knowledge of cGMP, ICH, and regulatory guidelines.
  • Must have hands-on experience managing global CTLs and CDMOs.
  • Must have strong technical expertise in separation science, such as liquid chromatography or mass spectrometry.
  • Must have strong technical experience in at least one of the modalities: monoclonal antibody and/ or oligonucleotide.
  • Must have experience in method development, validation, and lifecycle management for QC methods.
  • Good to have experience in complex drug products, such as co-formulation, multi-components, conjugates, etc.
  • Good to have experience in extended characterization & comparability studies to support BLA submission.
  • Good to have experience in authoring technical and scientific documents for regulatory submissions, including IND and BLA filings.
  • Good to have late phase experience, such as PPQ and commercialization.
  • Candidates proficient in both English and Mandarin are highly encouraged to apply.
  • Ability to work in a fast-paced virtual environment.
  • Flexibility to travel domestically and internationally as required.
  • Excellent communication, leadership, organizational and project management skills.
Working Conditions:
  1. Specify work environment:
  • Work from home.
  • Domestic and international travel up to 25%.
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range for Assoc Director and Director levels: $165-$245K
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
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