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Entry Level Cdmo Jobs (NOW HIRING)

Tissue Processing Tech 1

West Lafayette, IN · On-site

$17 - $20/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in ... from entry-level to highly skilled technician. New team members start with hands-on, one-on-one ...

Associate Process Technician

High Point, NC · On-site

  • Medical

  • Life

  • Retirement

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Job Overview The Associate Process Technician is an entry level role that will assist with ...

People & Culture Operations Partner

Holly Springs, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Overview The People and Culture (P&C) Operations Associate provides entry-level ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

Technician- Biomanufacturing, Upstream

Madison, WI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and ... This is an entry level position in the Manufacturing team and is the starting point to acquiring ...

Showing results 21-40

Entry Level Cdmo information

What is an entry level CDMO?

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 skills and qualifications are needed for an entry level CDMO?

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 challenges do entry level CDMO professionals face?

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 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:

Infographic showing various Entry Level Cdmo job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution.

Visual Inspection Technician I - 2nd Shift

Alcami Corporation

Charleston, SC • On-site

$18 - $23/hr

Full-time

Re-posted 21 days ago


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Visual Inspection Technician I is accountable for results in a fast-paced environment and responsible to perform tasks for the quality inspection of sterile injectable products for commercial distribution and clinical trials. The Visual Inspection Technician handles and inspects manufactured products by following standard operation procedures (SOPs) and batch records in accordance with current Good Manufacturing Practices (cGMPs). In addition, the Visual Inspection Technician employs acceptable techniques while working in manufacturing environments, including PPE gowning.

On-Site Expectations
  • 100% on-site position.
  • 2nd Shift: Monday - Friday, 2:00pm - 10:30pm.
Responsibilities
  • Follows applicable SOPs and cGMPs to perform assigned duties and tasks.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Conducts visual inspection of sterile liquids in accordance with regulatory agency guidelines.
  • Visually identifies debris, air lines, and other defects in sterile liquids.
  • Documents activities in real time on controlled documentation and legibly, per SOPs and cGMPs.
  • Performs component counting and basic math calculations.
  • Performs cleaning of rooms, tools, and equipment.
  • Performs specific visual inspections per SOPs.
  • Ensures product meets appearance specifications before sending the product for packaging.
  • Performs bulk packaging for product vials for shipment to another facility.
  • Operates material handling equipment.
  • Works occasional hours outside of scheduled shift based on business needs, which may include weekend work.

  • Other duties as assigned.
Qualifications
  • High school diploma or GED required. Associate degree preferred.
  • Entry level, 1+ years of relevant work experience strongly preferred OR BioWork certification from an accredited institution.
  • Relevant work experience in roles with visual inspection in regulated environments (i.e. medical field, electronics, aerospace, automotive production) are applicable. 
  • cGMP or prior work experience in a regulated environment preferred.
  • Prior pharmaceutical or CDMO experience preferred.
Knowledge, Skills, and Abilities
  • 20/20 correctable near-sighted vision in both eyes, tested annually required.
  • Ability to see and distinguish colors required.
  • Ability to perform basic math calculations, including product accountability calculations and rounding required.
  • Ability to read and comprehend detailed written instructions required.
  • Ability to move materials throughout the facility using appropriate methods and equipment required.
  • Excellent verbal and written communication, documentation, detail orientation and organizational skills required.
  • Proficiency in basic computing skills required.
  • Awareness of or prior experience with cGMP practices and procedures preferred.
Travel Expectations
  • Up to 5% domestic travel.
Physical Demands and Work Environment

The physical demands and work environment characteristics described here are representative of those that must be met or encountered by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to walk; climb or balance and stoop, kneel, crouch or crawl. The employee is required to sit for extended periods. The employee must regularly lift and/or move up to 50 pounds with assistance. Specific vision abilities required by this job include correctable 20/20 near vision, 20/20 distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions, risks of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

Employment Type: FULL_TIME

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