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Full Time Pharmaceutical Manufacturing Jobs (NOW HIRING)

$20 - $24/hr

Full-Time, Non-Exempt/Hourly Professional, Over-time elgibleWork Location:Fall River, MA Work Hours ... Minimum one (1) year of manufacturing experience with pharmaceutical or aerosol products.

Manufacturing Operator

Baudette, MN · On-site

$22 - $26/hr

NEW $2,500 SIGN ON BONUS for Full Time! Key Responsibilities (Vary by Level) All levels contribute to safe, efficient, and compliant pharmaceutical manufacturing. Responsibilities may include ...

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S.-based sterile manufacturing facility designed to meet the highest FDA and global cGMP standards ... • Full-time, on-site position in Langhorne, Pennsylvania • Monday-Friday schedule, with ...

Job Type Full-time Description The Pharmaceutical Manufacturing Technician is responsible for dispensing prescribed amounts of raw material for use in manufacturing; granulating, drying, blending ...

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Full Time Pharmaceutical Manufacturing information

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How much do full time pharmaceutical manufacturing jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for full time pharmaceutical manufacturing in the United States is $27.12, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.73 per hour, depending on experience, location, and employer.

What is the difference between Full Time Pharmaceutical Manufacturing vs Full Time Pharmaceutical Quality Control?

AspectFull Time Pharmaceutical ManufacturingFull Time Pharmaceutical Quality Control
CredentialsTypically requires a degree in pharmacy, chemistry, or related fieldRequires similar degrees, often with additional certifications in quality assurance
Work EnvironmentProduction floors, manufacturing plants, laboratoriesLaboratories, testing facilities, quality assurance departments
Employer & Industry UsageManufacturing companies, pharmaceutical plantsQuality control labs, pharmaceutical companies
Common Search & Comparison IntentUnderstanding manufacturing roles in pharmaComparing quality assurance roles in pharma

Full Time Pharmaceutical Manufacturing involves producing medications on the production line, focusing on assembly, processing, and packaging. In contrast, Full Time Pharmaceutical Quality Control emphasizes testing and ensuring the quality and safety of pharmaceutical products. Both roles require relevant degrees and are integral to the pharmaceutical industry, but they focus on different stages of the drug development and production process.

What is full time pharmaceutical manufacturing?

Full time pharmaceutical manufacturing involves working in facilities that produce medications and other pharmaceutical products on a regular, full-time schedule. Employees in this field may operate machinery, oversee production processes, ensure quality control, and adhere to strict safety and regulatory standards. The goal is to manufacture safe, effective, and high-quality pharmaceuticals for distribution to healthcare providers and patients. Full time roles typically offer standard benefits and require a commitment of around 40 hours per week.

What are some typical challenges faced by professionals in full-time pharmaceutical manufacturing roles?

Professionals in full-time pharmaceutical manufacturing often encounter challenges such as maintaining strict compliance with Good Manufacturing Practices (GMP), adapting to rapidly changing production schedules, and ensuring product quality under tight deadlines. Additionally, they must collaborate closely with cross-functional teams—including quality assurance, engineering, and research departments—to troubleshoot equipment issues and implement process improvements. Staying updated with regulatory requirements and technological advancements is also essential for long-term success in this role.

What are the key skills and qualifications needed to thrive as a Full Time Pharmaceutical Manufacturing professional, and why are they important?

To succeed in Full Time Pharmaceutical Manufacturing, you need a solid understanding of GMP (Good Manufacturing Practices), quality control, and safety protocols, often supported by a background in chemistry, biology, or a related field. Familiarity with manufacturing equipment, batch record systems, and regulatory compliance software is typically required, along with certifications like GMP or Six Sigma. Attention to detail, teamwork, and strong problem-solving abilities are crucial soft skills for this role. These competencies ensure safe, efficient production of high-quality pharmaceuticals that meet strict regulatory standards.
What cities are hiring for Full Time Pharmaceutical Manufacturing jobs? Cities with the most Full Time Pharmaceutical Manufacturing job openings:
What are the most commonly searched types of Pharmaceutical Manufacturing jobs? The most popular types of Pharmaceutical Manufacturing jobs are:
What states have the most Full Time Pharmaceutical Manufacturing jobs? States with the most job openings for Full Time Pharmaceutical Manufacturing jobs include:
Pharmaceutical Manufacturing Technician

Pharmaceutical Manufacturing Technician

Eurofins Scientific

Groton, CT

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted yesterday


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

57th of 105 rated laboratories


Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description
  • Generate, assist and execute documentation associated with manufacture, Batch Documents, Log Books, Labels, check sheets , protocols, Change control, QTS etc
  • Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product
  • Complete complex processing of intermediate bulk to convert this to a final patient ready final presentation
  •  Set up complex manufacturing equipment, manage and check documentation generated.
  • Complete activities associated with the operation and maintenance of a classified manufacturing space
  • Complete activities identified as operator care tasks associated with the maintenance and operation of complex manufacture equipment.
  • Generate, manage and report operational performance associated data
  • Identify, own and lead continuous improvement based projects
Qualifications
  • High school diploma 
  • Must hold a valid driver's license
  • Pharmaceutical manufacturing experience is a plus
  • The role requires a Groton site presence. The job requires the operation of manufacturing equipment in the Groton manufacturing area. Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required. Personal Protective Equipment, such as gloves, a full Tyvek suit, breathable air, and/or a filtering face piece, is often required.
  • Must be able to wear appropriate PPE (i.e,. daily uniform, safety glasses, respirator,s and full protective suits) when necessary
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to perform heavy lifting (up to 55lbs)
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • Strong computer, scientific, and organizational skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
  • Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed
  • May be requested to work on weekends, overtime, and holidays based on business needs.
  • Candidates currently living within a commutable distance of Ridgefield, CT are encouraged to apply.
  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.


What Eurofins employees say

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Benefits

Hours and flexibility

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US