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Evening Biopharmaceutical Science Jobs (NOW HIRING)

Eli Lilly and Company

TSMS- Sr. Scientist

Richmond, VA · On-site

$90K - $123K/yr

A minimum of 3 years of experience within the biopharmaceutical or GMP industry * Qualified ... As a manufacturing support function, the need for occasional evening or weekend support can arise.

Eli Lilly and Company

TSMS- Sr. Scientist

Richmond, VA · On-site

$90K - $123K/yr

A minimum of 3 years of experience within the biopharmaceutical or GMP industry * Qualified ... As a manufacturing support function, the need for occasional evening or weekend support can arise.

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How much do evening biopharmaceutical science jobs pay per year?

As of Sep 12, 2026, the average yearly pay for evening biopharmaceutical science in the United States is $48,391.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,500.00 and $52,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Biopharmaceutical Science jobs?

The most popular types of Biopharmaceutical Science jobs are:

Evening Biopharmaceutical Science jobs near you
Infographic showing various Evening Biopharmaceutical Science job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 72% Full Time, 23% Part Time, and 3% Contract. Highlights an 76% Physical, 3% Hybrid, and 21% Remote job distribution, with an average salary of $48,391 per year, or $23.3 per hour.

Technical Services & Manufacturing Science (TSMS) Scientist - Nights

Elwood, KS • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 13 days ago

Job description

Technical Services & Manufacturing Science (TSMS) Scientist, NightsResponsibilities
  • Provide technical and on-floor support for the commercialization, manufacture, and lifecycle management of monoclonal antibody products.
  • Collaborate with R&D, Manufacturing, and Quality to execute technical studies, validation activities, and technology transfer programs.
  • Support real-time troubleshooting; participate in investigations (root cause analysis for deviations, complaints, and OOS/OOE). Ensure proper documentation, CAPA development, and resolution within quality systems.
  • Serve as a subject matter expert for product and process in cross-functional teams, projects, and governance forums.
  • Use scientific and statistical tools to improve process understanding, maintain process control, and identify optimization/continuous improvement opportunities.
  • Lead and execute projects addressing process performance issues and driving measurable improvements.
  • Support resolution of technical and compliance-related issues, including preparing technical assessments/responses for internal audits and regulatory agencies.
Minimum Qualifications
  • Bachelor’s degree (or equivalent) in Bio/Pharmaceutical Technology, Microbiology, Engineering, or related discipline.
  • Working knowledge of biopharmaceutical production processes/technologies and experience in a cGMP-regulated environment.
  • Strong analytical and problem-solving skills; ability to provide technical troubleshooting and collaborate cross-functionally.
Preferred Qualifications
  • MSc or PhD in related discipline; 3+ years in biotech/pharma.
  • Experience with monoclonal antibody or recombinant protein manufacturing.
  • Experience in tech transfer, scale-up, and validation.
  • Familiarity with SAP, JMP, Veeva Vault; technical writing.
  • Experience applying RCI, FMEA, QRM.
  • Knowledge of USDA and/or EU GMP regulations for veterinary biologics.
Additional Information
  • Location: Elwood, Kansas; Night shift with weekend/evening rotation; Travel: minimal.
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