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Program Biotech Jobs in Cottleville, MO (NOW HIRING)

TekWissen LLC

Analytical Chemist

Chesterfield, MO · On-site

$32/hr

This client is a German multinational Pharmaceutical and biotechnology company and one of the ... Sciences Program) to support active ingredients analyses within R&D formulations and products.

JLL

Senior Facilities Manager

Chesterfield, MO

Manage preventive and corrective maintenance programs for critical utilities such as HVAC, clean ... pharmaceutical, biotech, or similarly regulated environments * Demonstrated expertise in GMP ...

Actalent

QC Scientist I

Saint Louis, MO

$28 - $31/hr

Experience in a GMP, GLP, pharmaceutical, or biotechnology laboratory. * Experience with SEC, CEX ... Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a ...

Bestzyme

Sr./ Sales Manager, Sweet Protein

Saint Louis, MO · Remote

$100K - $130K/yr

Our accomplished team is driven to harness the power of biotechnology to accelerate sustainable and ... We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs ...

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Showing results 21-40

All JobsProgram Biotech JobsProgram Biotech Jobs in Cottleville, MO

Program Biotech information

See Cottleville, MO salary details

$20.1K

$42K

$72.7K

How much do program biotech jobs pay per year?

As of Aug 20, 2026, the average yearly pay for program biotech in Cottleville, MO is $42,038.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,100.00 and $47,800.00 per year, depending on experience, location, and employer.

What is a program biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What are the key skills and qualifications needed to thrive as a program biotech professional?

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.

What are some common challenges faced by program biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What job categories do people searching Program Biotech jobs in Cottleville, MO look for?

The top searched job categories for Program Biotech jobs in Cottleville, MO are:

Program Biotech jobs near you

Global Product Registration Manager

Pivot Bio

Saint Louis, MO • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Job description

About Pivot Bio:
Fueled by an innovative drive and a deep understanding of microbiology, genomics, crop nutrition and agriculture, Pivot Bio is pioneering game-changing advances in fertilizer technology. Our first commercial product harnesses the power of naturally-occurring microbes, modern gene editing and application technologies to provide nitrogen to crops. We are dedicated to providing new solutions for farmers to improve yield as they work to help feed the world's growing population. Read/Hear more about Pivot Bio on Forbes or PBS News Hour.
The Global Product Registration Manager will lead regulatory strategy and execution for the registration and commercialization of Pivot Bio products, with a strong emphasis on United States federal and state regulatory requirements. This role is responsible for ensuring timely product approvals, maintaining compliance across jurisdictions, and enabling market access through proactive engagement with regulatory authorities.
Essential Functions
  • Develop and execute global regulatory strategies for Pivot Bio products, with primary focus on U.S. regulatory frameworks, including federal and state-level registrations (e.g., soil amendment, biostimulant, and biofertilizer requirements).
  • Lead the preparation, submission, and management of regulatory dossiers to U.S. agencies and individual state departments of agriculture, ensuring alignment with varying state data requirements, labeling standards, and review timelines.
  • Coordinate and manage state registration processes across all states required for product commercial launch, including renewals, amendments, and tonnage reporting
  • Serve as the primary regulatory contact for U.S. state agencies, building relationships and effectively responding to inquiries and data requests.
  • Interpret evolving regulatory guidance related to gene-edited organisms, microbial products, and biotechnology, translating requirements into actionable plans.
  • Partner cross-functionally with regulatory science, product development, manufacturing, quality, and commercial teams to create product labels and compile data packages supporting product safety, efficacy, and environmental impact.
  • Partner with growth team to inform new partnership strategy with regards to potential regulatory pathways, requirements, resources, and timelines.
  • Forecast product registration resource needs based on commercial plans and build resources internally and/or externally to meet commercial timelines
  • Monitor regulatory developments at both federal and state levels, identifying risks and opportunities, and advising internal stakeholders on strategic implications.
  • Ensure compliance with post-registration obligations, including adverse event reporting, tonnage reporting, and label updates.
  • Support global registrations outside the U.S. as needed, ensuring consistency in regulatory strategy and documentation.
  • Contribute to regulatory policy and advocacy efforts through engagement with industry groups and stakeholders.
Competencies
Knowledge & Application
  • Demonstrated experience with U.S. federal and state registration processes, particularly for microbial products such as biopesticides, biofertilizers, or biostimulants.
  • Strong working knowledge of U.S. regulatory agencies and frameworks, including familiarity with state-specific requirements and registration systems.
  • Experience preparing and submitting regulatory dossiers, including data related to product characterization, toxicology, environmental fate, and efficacy.
  • Understanding of gene editing technologies (e.g., CRISPR) and their regulatory implications preferred.
  • AI proficiency, including the ability to responsibly leverage AI-enabled tools to improve regulatory research, dossier development, data synthesis, workflow efficiency, and cross-functional decision support.
Complexity & Problem Solving
  • Proven ability to manage multiple complex projects and regulatory submissions simultaneously.
  • High attention to detail, strong organizational skills, and a proactive, solutions-oriented mindset.
Collaboration & Interaction
  • Excellent communication, technical writing, and stakeholder engagement skills.
  • Ability to work effectively in a cross-functional, global environment and influence without direct authority.
  • Collaborate cross-functionally with regulatory science, product development, manufacturing, quality, and commercial teams
Required Education & Experience
  • Bachelors degree in Microbiology, Molecular Biology, Biotechnology, Plant Sciences, or a related scientific discipline.
  • Minimum of 8 years of regulatory affairs experience in agricultural biologicals, biotechnology, or related industry.
Must be authorized to work in the United States
What We Offer:
  • Incentive Bonus Plan
  • Competitive package in a disruptive startup
  • Stock options
  • Health/Dental/Vision insurance with employer-paid premiums
  • Life, Short-Term and Long-Term Disability policies
  • Employee Assistance Program with free referrals and discounts
  • 401(k) plan, 3% Match
  • Commuter benefits
  • Annual Training & Development support
  • Flexible vacation policy with a generous holiday schedule
  • Exciting opportunity to work with a talented and fun team

#LI-Onsite
Hiring Compensation Range
$105,984-$132,480 USD

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