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Biopharma Jobs in Tennessee (NOW HIRING)

About Sanofi We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative ...

New

Head, US E-Commerce

Morristown, TN · On-site

$200 - $250/hr

About Sanofi We're an R&D‑driven, AI‑powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative ...

New

Phlebotomist

Cleveland, TN · On-site

$13 - $16.50/hr

Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help ...

Phlebotomist

La Vergne, TN · On-site

$16.25 - $20.25/hr

Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help ...

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Biopharma information

See Tennessee salary details

$16

$48

$96

How much do biopharma jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for biopharma in Tennessee is $48.89, according to ZipRecruiter salary data. Most workers in this role earn between $31.06 and $59.93 per hour, depending on experience, location, and employer.

What is a biopharma?

A Biopharma job involves working in the biotechnology and pharmaceutical industries to research, develop, manufacture, or market biological drugs and therapies. Professionals in this field may work in roles such as research scientist, regulatory affairs specialist, manufacturing associate, or quality control analyst. Their work focuses on creating innovative treatments using biotechnology, like monoclonal antibodies, gene therapies, or vaccines. Careers in biopharma require expertise in biology, chemistry, engineering, or related fields and often involve collaboration with regulatory agencies to ensure product safety and efficacy.

What are the key skills and qualifications needed to thrive in biopharma?

To thrive in the biopharma industry, a strong background in life sciences, such as biology, chemistry, or pharmaceutical sciences, and relevant advanced degrees or experience are essential. Familiarity with laboratory techniques, regulatory compliance systems (like FDA or EMA guidelines), and specialized software for data analysis or clinical trials is typically required. Excellent analytical thinking, teamwork, and strong communication skills help professionals collaborate effectively and drive successful project outcomes. These abilities are important because the field demands rigorous scientific support, precise regulatory adherence, and effective multidisciplinary teamwork to advance new pharmaceutical products.

What are some typical career advancement opportunities in the biopharma industry?

The biopharma industry offers a range of career advancement paths, starting from entry- or associate-level scientific roles to more senior positions like project manager, lead scientist, or regulatory affairs specialist. With experience, professionals can transition into leadership roles overseeing research teams, clinical trial management, or move toward specialized areas like quality assurance, business development, or medical affairs. Many companies also support ongoing professional development through training, certifications, and opportunities to participate in high-impact projects. Advancement is often based on expanding technical expertise, strong performance, and the ability to successfully deliver results within cross-functional teams. This dynamic field rewards continuous learning and offers clear pathways for growth within both scientific and business tracks.

What are the most commonly searched types of Biopharma jobs in Tennessee?

The most popular types of Biopharma jobs in Tennessee are:

What are popular job titles related to Biopharma jobs in Tennessee?

For Biopharma jobs in Tennessee, the most frequently searched job titles are:

Infographic showing various Biopharma job openings in Tennessee as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, 3% Contract, and 1% Nights. Highlights an 77% Physical, 4% Hybrid, and 19% Remote job distribution, with an average salary of $101,696 per year, or $48.9 per hour.

Assistant Plasma Center Manager

Kedrion Biopharma GmbH

Cleveland, TN • On-site

$60 - $80/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Key responsibilities

  • Support the Center Manager in overseeing daily plasma collection operations and ensuring compliance with SOPs, FDA, EMEA, and customer specifications.

  • Assist in managing staff scheduling, training, and performance to maintain operational efficiency and team effectiveness.

  • Monitor equipment, inventory, and quality control processes, including responding to alarms and participating in deviation management.


Job description

KEDPLASMA is a subsidiary of Kedrion Biopharma Inc. KEDPLASMA specializes in the collection and procurement of high-quality plasma that is processed into plasma-based therapies. Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help treat and prevent serious diseases, including Hemophilia, Primary Immune System Deficiencies, and Rh-Sensitization.

Job Summary

Are you a proactive leader who thrives in a fast-paced, regulated environment?

Join our team as an Assistant Manager and help drive operational excellence, donor satisfaction, and team performance at our plasma collection center. In this role, you’ll support the Center Manager in overseeing daily operations, ensuring compliance, and fostering a culture of safety, quality, and care.

As Assistant Manager, you’ll be involved in every aspect of center performance—from staffing and scheduling to equipment oversight and regulatory compliance. You’ll help lead a dedicated team and ensure the center runs smoothly, efficiently, and in alignment with company standards.

What you'll do
  • Promote professional customer service and donor retention through staff coaching and support.
  • Ensure all center activities comply with SOPs, FDA, EMEA, and customer specifications.
  • Maintain operational efficiency and fiscal responsibility in accordance with cGMP and QAP standards.
  • Support special donor programs, including titer testing and antibody identification.
  • Oversee completion of daily logs and records, including temperature checks and quality control.
  • Collaborate with management to ensure appropriate staffing and coverage for donation volumes.
  • Maintain accurate personnel records, including evaluations, training, and attendance.
  • Assist in scheduling and preparing for staff changes, vacations, and absenteeism.
  • Identify and address quality or compliance issues proactively.
  • Monitor inventory levels and ensure adequate stock for production needs.
  • Manage equipment maintenance schedules and resolve equipment issues promptly.
  • Respond to freezer alarms and resolve excursions to protect product quality.
  • Participate in deviation management, including documentation, investigations, and CAPA implementation.
  • Perform opening and closing duties, including equipment checks, documentation, security protocols, etc.
Qualifications and need-to-know
  • Bachelor’s degree in healthcare, life sciences, business administration, or related field preferred (or equivalent experience).
  • Minimum 1 year of supervisory or management experience, ideally in a plasma or regulated environment.
  • Knowledge of plasma operations, FDA, CLIA, and cGMP regulations preferred.
  • Strong organizational and leadership skills.
  • Proficiency in Microsoft Office and data entry systems.
  • Ability to manage multiple priorities and maintain compliance in a dynamic setting.
  • Comfortable working in regulated environments with exposure to bloodborne pathogens and cold storage.

Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.

Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Salary ranges are determined based on relevant experience, education, and certifications.
If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at kedtalent@kedrion.com.

Employee Benefits:

At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including:

  • Health & Wellness – Full medical, dental, and vision coverage
  • Financial Security – Life insurance, AD&D, and retirement savings plans
  • Work-Life Balance – Paid time off, sick leave, and paid holidays
  • Career Growth – Training programs and development opportunities
  • Extra Perks – Employee discounts, wellness initiatives, and more!

Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.

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