Senior Biologist

Posted 8 Days Ago
Be an Early Applicant
2 Locations
Hybrid
Senior level
Pharmaceutical • Manufacturing
The Role
Provides scientific leadership for developing, validating, transferring, and applying biological assays supporting biotherapeutic characterization, quality control, manufacturing investigations, and product lifecycle management. Leads cell-based potency, protein characterization, and molecular biology methods; troubleshoots complex analytical challenges; manages CROs and cross-functional projects; interprets data and prepares technical and regulatory documentation. Ensures compliance with GMP, FDA, ICH, and USP expectations while contributing to assay modernization, innovation, and regulatory strategy.
Summary Generated by Built In

Job Title

Senior Biologist

Requisition

JR000015998 Senior Biologist (Open)

Location

St. Louis, MO

Additional Locations

Hazelwood, MO

Job Description Summary

Keenova Therapeutics is seeking a highly motivated and experienced Senior Biologist to join the Global Technical Operations team. This role will provide scientific leadership in the development, validation, transfer, and application of biological assays to support the characterization, quality control, and lifecycle management of biotherapeutic products and manufacturing materials. Responsibilities include development of cell-based potency assays and protein and gene expression characterization methods. The successful candidate will collaborate across functions to support assay modernization initiatives, product development, manufacturing investigations, and regulatory activities.

Job Description

  • Serve as a technical leader in cell and molecular biology, leading development, validation, and transfer of biological assays for biotherapeutic products.
  • Design, develop, optimize, and validate cell-based potency assays, protein characterization methods, and molecular biology assays in accordance with current regulatory expectations.
  • Apply expertise in protein and gene expression analysis, including mammalian cell culture, cell-based assays, PCR/qPCR, Western blotting, ELISA, flow cytometry, and related methodologies.
  • Provide technical troubleshooting and scientific guidance to resolve complex analytical and biological challenges.
  • Characterize proteins, peptides, raw materials, intermediates, drug substances, and drug products to support manufacturing, investigations, and product lifecycle management.
  • Lead CROs and cross-functional teams to execute projects and achieve development objectives.
  • Work with PM to establish project timelines, coordinate functional activities, and ensure delivery of milestones.
  • Evaluate data, interpret results, and prepare technical reports suitable for internal stakeholders and regulatory submissions.
  • Demonstrate excellent verbal and written communication skills. Responsible for clear communication in both written and oral forms to a broader audience.
  • Collaborate effectively with Process Chemistry, Formulation, Analytical Development, Manufacturing, Quality, Operations, and Regulatory Affairs teams.
  • Contribute to scientific innovation through implementation of new technologies, publications, intellectual property, and technical know-how.
  • Ensure activities comply with applicable GMP requirements and regulatory guidelines.
  • Maintain complete and accurate laboratory documentation and follow established safety practices.

DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:

  • Working knowledge of FDA, ICH, and USP requirements applicable to biological assays and product characterization.
  • Support preparation of technical summaries, reports, and documentation for regulatory submissions and health authority interactions.
  • Contribute to development of regulatory strategies related to assay validation, comparability, and product characterization.

Qualifications:

Education:

  • Ph.D. in Biology, Molecular Biology, Cell Biology, Biochemistry, Biotechnology, or a related life science discipline.
  • M.S. or B.S. in a related scientific discipline may be considered with appropriate industry experience.

Experience:

  • Ph.D. with 5+ years of relevant pharmaceutical or biotechnology industry experience.
  • MS with 7+ years of relevant pharmaceutical or biotechnology industry experience.
  • B.S. with 10+ years of pharmaceutical or biotechnology industry experience.

Competencies:

  • Demonstrated expertise in development, qualification, validation, and transfer of cell-based potency assays and biological methods.
  • Experience with mammalian cell culture, biotherapeutic product characterization, and development of cell-based potency assays is strongly preferred.
  • Extensive hands-on experience with protein characterization techniques, including Western blotting, ELISA, and automated capillary immunoassay platforms such as ProteinSimple Jess or Peggy Sue.
  • Experience with molecular biology methods including PCR, qPCR, RT-qPCR, and gene expression analysis.
  • Experience supporting product investigations, process understanding, and manufacturing-related technical studies is highly desirable.
  • Knowledge of GMP regulations, assay validation principles, and regulatory expectations for biological products.
  • Experience with LC-MS, proteomics, and advanced protein characterization techniques is desirable.
  • Strong scientific and technical expertise in cell and molecular biology.
  • Demonstrated leadership and CRO management capabilities.
  • Excellent analytical thinking and problem-solving skills.
  • Strong written and verbal communication skills.
  • Ability to work independently while effectively collaborating within cross-functional teams.
  • Strong organizational skills and attention to detail.
  • Proficiency with Microsoft Office applications and scientific data analysis software.
  • Ability to communicate effectively with technical teams, leadership, and external collaborators.

Organizational Relationship/Scope:

  • Reports to Senior Director, Global Technical Operations

Working Conditions:

  • Hybrid / Onsite

Keenova offers employees a Total Rewards package which includes competitive pay and benefits. To learn more about our Total Rewards benefits please visit: Keenova Careers | Serve and Grow with Purpose | Keenova


Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.


#LI-HYBRID

#LI-GN1

At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support—showing up in big moments and small to help patients find comfort and confidence.

 

We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology, men’s health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.

 

We are Keenova—keen to solve, keen to serve. Learn more at www.keenova.com.

Skills Required

  • Ph.D. in Biology, Molecular Biology, Cell Biology, Biochemistry, Biotechnology, or a related life science discipline; an M.S. or B.S. may be considered with appropriate industry experience.
  • Ph.D. with at least 5 years of relevant pharmaceutical or biotechnology industry experience.
  • M.S. with at least 7 years of relevant pharmaceutical or biotechnology industry experience.
  • B.S. with at least 10 years of pharmaceutical or biotechnology industry experience.
  • Expertise in development, qualification, validation, and transfer of cell-based potency assays and biological methods.
  • Experience with mammalian cell culture, biotherapeutic product characterization, and cell-based potency assays.
  • Hands-on experience with Western blotting, ELISA, and automated capillary immunoassay platforms such as ProteinSimple Jess or Peggy Sue.
  • Experience with PCR, qPCR, RT-qPCR, and gene expression analysis.
  • Knowledge of GMP regulations, assay validation principles, and regulatory expectations for biological products.
  • Experience supporting product investigations, process understanding, and manufacturing-related technical studies.
  • Experience with LC-MS, proteomics, and advanced protein characterization techniques.
  • Strong scientific and technical expertise in cell and molecular biology.
  • Demonstrated leadership and CRO management capabilities.
  • Excellent analytical thinking, problem-solving, written communication, and verbal communication skills.
  • Ability to work independently and collaborate effectively with cross-functional teams.
  • Strong organizational skills and attention to detail.
  • Proficiency with Microsoft Office applications and scientific data analysis software.
  • Working knowledge of FDA, ICH, and USP requirements applicable to biological assays and product characterization.
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Hazelwood, MO
2,700 Employees
Year Founded: 1867

What We Do

Mallinckrodt Pharmaceuticals plc is a global specialty pharmaceutical company with over 150 years of experience. Historically a manufacturer of specialty pharmaceuticals, generic drugs, and imaging agents, the company transitioned in November 2025 to be known as Keenova Therapeutics. It now focuses on developing, manufacturing, and commercializing branded therapeutics designed to help patients with rare or unaddressed conditions live healthier and happier lives.

Similar Jobs

Wells Fargo Logo Wells Fargo

Senior Counsel

Fintech • Financial Services
Hybrid
Saint Louis, MO, USA
205000 Employees
139K-260K Annually

MetLife Logo MetLife

Business Analyst

Fintech • Information Technology • Insurance • Financial Services • Big Data Analytics
Remote or Hybrid
United States
43000 Employees
42K-55K Annually

Samsara Logo Samsara

Firmware Engineer

Artificial Intelligence • Cloud • Computer Vision • Hardware • Internet of Things • Software
Easy Apply
Remote or Hybrid
United States
4000 Employees
155K-290K Annually

PwC Logo PwC

Procurement Strategy and Strategic Sourcing - Value Capture Senior Associate

Artificial Intelligence • Professional Services • Business Intelligence • Consulting • Cybersecurity • Generative AI
Hybrid
56 Locations
370000 Employees
77K-202K Annually

Similar Companies Hiring

Fortune Brands Innovations Thumbnail
Manufacturing
Deerfield, IL
10000 Employees
Rosendin Thumbnail
Other • Manufacturing
San Jose, CA
6219 Employees
Amalgamated Sugar Thumbnail
Food • Greentech • Agriculture • Industrial • Manufacturing
Boise, Idaho
768 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account