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Clinical Manufacturing Jobs (NOW HIRING)

3 Key Consulting

$32 - $34/hr

Associate Engineer, Clinical Mfg. and Lab Support Drug Delivery Devices - (JP14416) Location: Thousand Oaks, CA. 91320 Employment Type: Contract Business Unit: CPO Process Engineering Duration: 2+ ...

GeneFab

Sr. Manager/Manager, Manufacturing

Alameda, CA · On-site

Support capacity planning for clinical and commercial manufacturing campaigns; proactively identify and escalate resourcing or scheduling risks that could impact client program delivery. * Build and ...

GeneFab

Sr. Manager/Manager, Manufacturing

Alameda, CA · On-site

Support capacity planning for clinical and commercial manufacturing campaigns; proactively identify and escalate resourcing or scheduling risks that could impact client program delivery. * Build and ...

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Clinical Manufacturing information

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$14

$34

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How much do clinical manufacturing jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for clinical manufacturing in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What are some typical challenges faced in a Clinical Manufacturing role and how can they be addressed?

Professionals in Clinical Manufacturing often encounter challenges related to strict regulatory compliance, tight production timelines, and the need for precise documentation. These roles require close collaboration with quality assurance and regulatory teams to ensure that all processes meet Good Manufacturing Practice (GMP) standards. Addressing these challenges involves maintaining clear communication, thorough training, and a proactive approach to problem-solving, especially when scaling up production or introducing new clinical batches. Being detail-oriented and adaptable helps ensure product consistency and regulatory readiness.

What are the key skills and qualifications needed to thrive in Clinical Manufacturing, and why are they important?

To thrive in Clinical Manufacturing, you need a solid understanding of Good Manufacturing Practices (GMP), bioprocessing techniques, and quality assurance, often supported by a degree in life sciences or engineering. Familiarity with manufacturing execution systems (MES), aseptic processing equipment, and regulatory compliance tools is typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills in this role. These competencies ensure the reliable production of clinical materials that meet strict regulatory standards and support patient safety.

What is clinical manufacturing?

Clinical manufacturing refers to the specialized process of producing pharmaceutical or biotechnological products, such as drugs or vaccines, in quantities needed for clinical trials. This involves adhering to strict regulatory standards, such as Good Manufacturing Practices (GMP), to ensure product quality, safety, and consistency. Clinical manufacturing is a crucial step in drug development, bridging the gap between laboratory research and large-scale commercial production. It often includes activities like formulation, production, packaging, and labeling of investigational products used in human clinical studies.

What is the difference between Clinical Manufacturing vs Pharmaceutical Manufacturing?

AspectClinical ManufacturingPharmaceutical Manufacturing
CredentialsTypically requires GMP training, relevant science or engineering degreesRequires GMP training, degrees in pharmacy, chemistry, or related fields
Work EnvironmentLaboratories, small-scale production facilities, controlled environmentsLarge-scale production plants, extensive quality control labs
Industry UsageUsed in early-stage drug development, clinical trial material productionUsed in mass production of approved drugs for market distribution
Job FocusDeveloping and manufacturing small batches for clinical trialsMass production, quality assurance, and distribution of finished products

Clinical Manufacturing and Pharmaceutical Manufacturing share core GMP knowledge and work environments but differ mainly in scale and purpose. Clinical Manufacturing focuses on small-scale production for clinical trials, while Pharmaceutical Manufacturing involves large-scale production for commercial sale.

More about Clinical Manufacturing jobs
What cities are hiring for Clinical Manufacturing jobs? Cities with the most Clinical Manufacturing job openings:
What states have the most Clinical Manufacturing jobs? States with the most job openings for Clinical Manufacturing jobs include:
What job categories do people searching Clinical Manufacturing jobs look for? The top searched job categories for Clinical Manufacturing jobs are:
Clinical Manufacturing jobs near you
Infographic showing various Clinical Manufacturing job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 51% Full Time, 29% Part Time, and 15% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $72,002 per year, or $34.6 per hour.

Clinical Trial Labeling Specialist

Alsinova

Collegeville, PA • On-site, Remote

Other

Posted 3 days ago

Job description

ALSINOVA is hiring a Clinical Trial Labeling Specialist on hybrid model (remote + on-site)

Sites : Raleigh, NC or Greater Philadelphia, PA


Job Responsibilities

  • Work within a global team. Create master label content according to existing processes and procedures, designing Clinical Trial labels.
  • Perform quality critical checks of label content produced in various languages to required timelines.
  • Perform quality critical checks of externally produced vendor label proofs prior to receipt.
  • Creation of label documentation, required for in-country regulatory submissions, in a timely manner.
  • Highlight label quality issues.
  • Work with external vendors (translation service provider, component suppliers etc).
  • Participate in GPM team meetings. [GPM stands for Global Pack Management]
  • Liaise with other groups within Clinical Manufacturing & Supply Chain.
  • Work in key IT systems – SMARTLS Compliance Author, Adobe InDesign, Prisym 360.


Experience Required

  • Able to follow written instructions, shows a good degree of accuracy and attention to detail.
  • Good knowledge of Clinical Supply requirements, standards and GMP regulations.
  • Good understanding of Clinical Supplies packaging, labeling and distribution plus related paperwork.
  • Self-assign core tasks, prioritizing and completing as part of a wider team with minimal supervision/input.
  • Bachelor degree
  • 2 years of pharmaceutical experience including cGMP environment or compliance role or auditing role.
  • Experience with clinical trials is preferred.

Apply