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Full Time Pharmaceutical Manufacturing Jobs (NOW HIRING)

Cipla

$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.

Laser Photonics

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Sales Manager- Pharmaceutical Manufacturing (Capital Equipment)

Lake Mary, FL · On-site

$55K - $65K/yr

Sales Manager - Pharmaceutical Manufacturing (Capital Equipment) Laser Photonics Corporation ... Lake Mary, FL (On-Site) Employment Type: Full-Time About Laser Photonics Corporation Laser ...

ANI Pharmaceuticals

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 ...

Penn Life Sciences

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Industrial Maintenance Mechanic (Pharmaceutical)

Langhorne, PA · On-site

$30 - $40/hr

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 ...

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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 27, 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:
Full Time Pharmaceutical Manufacturing jobs near you
Pharmaceutical Manufacturing Technician

Pharmaceutical Manufacturing Technician

SHINE Technologies LLC

Janesville, WI • On-site

$25 - $32/hr

Full-time

Posted 11 days ago

Job description

Job Type
Full-time
Description
SHINE Technologies is seeking a Pharmaceutical Manufacturing Technician - 1st Shift, to perform production of medical radioisotopes and play a major part in growing our manufacturing operations as we start with clinical production and move into commercial production. The Pharmaceutical Manufacturing Technician will perform operations with focus on efficiency, quality and safety standards while using remote manipulators in cleanrooms to produce Lu-177.
Shift: Monday - Friday 6:00am - 2:30pm
The base salary range for this position is $25.00 - $32.00 per hour plus a comprehensive compensation package. Our salary ranges are determined by role, level, and location.
Duties and Responsibilities:
All below listed responsibilities must be completed in compliance with federal, state, local, and company-specific regulations related to quality of product, employee and customer safety, and to the proper performance of day-to-day operations. The essential functions of this position include, but are not limited to:
  • Maintain complete and accurate batch records and related documentation in accordance with cGMP/cGDP.
  • Prepare materials/consumables for the manufacturing processes of active pharmaceutical ingredient Lutetium Chloride and perform cleaning activities, line clearances, and system checks on equipment before use in aseptic processes.
  • Perform production tasks such as receiving raw materials, processing radioisotopes in production hot cells, preparing the sterile API and shipping the API to our customers.
  • Perform routine maintenance under direction or supervision of Manufacturing Engineer.
  • Support leadership team in identifying operational opportunities for continuous improvement, initiating changes to processes as needed.
  • Maintain general cleanliness of work area and assist other work areas as needed to ensure a clean and professional environment.
  • Utilize Quality Management System to document maintenance, investigations and change control actions.
  • Assist in writing deviations, investigations and initiate unscheduled work orders.
  • Strict adherence to cGMP at all times.
  • Assist in training and development of other technicians.
  • Assist other projects and departments and perform other duties as requested or assigned.

Requirements
  • Ability to follow and observe all radiation safety and pharmaceutical requirements, including successfully passing all gown qualifications.
  • Associate degree plus a minimum of one year experience or high school diploma with 2 or more years of experience in areas such as pharmaceutical or API manufacturing, equipment operator, and food processing.
  • Strong mathematical skills including algebra.
  • Experience drafting documents such as SOPs and batch records required
  • Experience working with radioactive materials and/or radioisotope production is a plus.
  • Aseptic experience preferred
  • Willingness to learn and understand new technology, instrumentation and technical processes.
  • Ability to read from engineering drawings or schematics.
  • Ability to follow written procedures and accurately record test data.
  • Ability to work safely within an industrial and radiation environment.
  • The position will require non-standard work hours and shift work, on a periodic, rotational or ongoing basis. Overtime may sometimes be necessary to complete required work assignment with little or no advance notice.
  • Some travel may be required.

Eligibility for employment is conditioned on the applicant's ability to qualify for access to information subject to U.S. Export Controls. Additionally, applicant's eligibility may be conditioned based upon meeting the Nuclear Regulatory Commission requirements for access to Safeguards Information, which typically requires a pre-employment drug screen, fingerprinting and criminal background check.
SHINE values diversity in all its forms as a critical component of innovation, which is fundamental to our success. Every member of the SHINE community benefits from the talents and experiences of our peers, from the mutual respect we exercise, and from the responsibility we take for our actions.
SHINE Technologies, LLC maintains affirmative action plans for individuals with disabilities and protected veterans. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Pay Transparency Policy
Employee Rights Under the NLRA
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