2

Entry Level Cdmo Jobs (NOW HIRING)

QC Chemist I

San Diego, CA · On-site

$68K - $71K/yr

... CDMO), and Catalent's San Diego facility focuses on early-stage development of small molecule and ... This entry level position gives opportunities to broaden analytical understanding and learn the ...

QC Chemist I

San Diego, CA · On-site

$68K - $71K/yr

... CDMO), and Catalent's San Diego facility focuses on early-stage development of small molecule and ... This entry level position gives opportunities to broaden analytical understanding and learn the ...

QC Technician (Weekend Shift)

Fishers, IN · On-site

$18.50 - $23.50/hr

This entry-level role focuses on accurate execution, strong Good Documentation Practices (GDP), and ... At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture ...

Technician I Staging - Supply Chain

Madison, WI · On-site

$42.30K - $51.90K/yr

... CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and ... This is an entry level non-laboratory role that will allow you to acquire the skills to work in a ...

next page

Showing results 1-20

Entry Level Cdmo information

What are the key skills and qualifications needed to thrive as an Entry Level CDMO (Contract Development and Manufacturing Organization) professional, and why are they important?

To thrive as an Entry Level CDMO professional, you generally need a bachelor’s degree in life sciences, chemistry, or a related field, along with a solid understanding of laboratory techniques and GMP (Good Manufacturing Practice) principles. Familiarity with analytical instruments, LIMS (Laboratory Information Management Systems), and regulatory documentation is typically required. Attention to detail, teamwork, and strong communication skills help you excel in collaborative, compliance-driven environments. These skills and qualities are crucial for ensuring product quality, regulatory adherence, and smooth workflow in pharmaceutical development and manufacturing.

What are some common challenges faced by entry-level professionals in a CDMO (Contract Development and Manufacturing Organization) environment?

Entry-level professionals in a CDMO often encounter challenges such as adapting to fast-paced project timelines, learning to work with strict regulatory guidelines, and collaborating with cross-functional teams from diverse backgrounds. Since CDMOs serve multiple clients with varying requirements, priorities can shift quickly, requiring flexibility and strong organizational skills. However, these challenges also provide excellent opportunities for rapid learning and professional growth, as new hires are exposed to a wide variety of projects and industry practices.

What are entry level CDMO positions?

Entry level CDMO positions are jobs at Contract Development and Manufacturing Organizations (CDMOs) that are suitable for candidates with little to no prior experience in the pharmaceutical or biotechnology industry. These roles may include positions in quality control, manufacturing, laboratory support, or administrative assistance. Entry level CDMO jobs provide a valuable opportunity to learn about drug development and manufacturing processes while gaining hands-on experience in a regulated environment. They often serve as a stepping stone to more specialized or advanced roles within the industry.

What is the difference between Entry Level Cdmo vs Entry Level Contract Manufacturing Organization (CMO)?

AspectEntry Level CdmoEntry Level Contract Manufacturing Organization (CMO)
Required CredentialsBachelor's in life sciences, chemistry, or related fieldBachelor's in sciences or engineering, relevant certifications
Work EnvironmentPharmaceutical or biotech labs, manufacturing facilitiesManufacturing plants, production lines, client sites
Employer & Industry UsagePharmaceutical companies, biotech firmsContract manufacturing companies serving pharma/biotech
Common Search & ComparisonYesYes

Entry Level Cdmo roles typically involve supporting drug development and manufacturing processes within a CDMO, focusing on laboratory work and process optimization. Entry Level CMO positions are more centered on manufacturing and production activities within a contract manufacturing organization. Both roles require similar educational backgrounds and are used within the pharmaceutical and biotech industries, but they differ mainly in their focus areas—development versus manufacturing.

More about Entry Level Cdmo jobs
What cities are hiring for Entry Level Cdmo jobs? Cities with the most Entry Level Cdmo job openings:
What are the most commonly searched types of Cdmo jobs? The most popular types of Cdmo jobs are:
What job categories do people searching Entry Level Cdmo jobs look for? The top searched job categories for Entry Level Cdmo jobs are:
Infographic showing various Entry Level Cdmo job openings in the United States as of May 2026, with employment types broken down into 21% Locum Tenens, 8% Full Time, 17% Temporary, 50% Contract, and 4% Summer. Highlights an 99% Physical, and 1% Remote job distribution.
Technician - Biomanufacturing, Central Services

Technician - Biomanufacturing, Central Services

Catalent Pharma Solutions

Madison, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 70 rated pharmaceutical


Job description

Technician - Biomanufacturing, Central Services

Position Summary:

  • Work Schedule: 6am-4pm (Sunday-Wednesday or Wednesday-Saturday shift availability)
  • 100% on-site

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

This is an entry level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment. The position is expected to follow detailed instructions and established procedures with frequent supervision.

The Role:

  • Perform basic buffer preparation activities, including weighing raw materials for production
  • Accurately follows manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on "right first time" execution
  • Documents all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation
  • Recognizes deviations from the intended procedure and raises awareness through the Rapid Response process
  • Proactively identifies safety, quality, and efficiency improvements; Actively participates in the Catalent Way (Continuous Improvement Culture)
  • May lead "Just Do It" (JDI) Continuous Improvement (CI) activities and engage in implementation of CI projects
  • May coach more junior team members on basic execution activities and act as an "onboarding buddy" to facilitate bringing new team members quickly up to speed on culture and basic workplace expectations
  • Performs general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards
  • Other duties as assigned

The Candidate:

  • Must have High School Diploma or equivalent. No additional experience required
  • GMP manufacturing experience preferred
  • Ability to use Microsoft Word and Excel, and other Office systems
  • GMP manufacturing experience preferred
  • Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software
  • Physical requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed.

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 hours of PTO + 8 paid holidays
  • Generous 401K match
  • Medical, dental and vision benefits
  • Tuition Reimbursement- Let us help you finish your degree or start a new degree!

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Catalent logo

About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media