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Part Time Pharmaceutical Manufacturing Jobs (NOW HIRING)

Senior Process Engineer

Chandler, AZ

$102K - $132K/yr

Telework Type: Part-Time Telework * Work Location: Chandler, AZ Extraordinary teams building ... Industry experience in semiconductor or pharmaceutical manufacturing environments. * Familiarity ...

Senior Process Engineer

Chandler, AZ · On-site

$102K - $132K/yr

Telework Type: Part-Time Telework * Work Location: Chandler, AZ Extraordinary teams building ... Industry experience in semiconductor or pharmaceutical manufacturing environments. * Familiarity ...

Pharmacist Intern (Part-time)

Richmond, VA · On-site

$16.50 - $20.50/hr

We cultivate, manufacture, and sell a broad portfolio of high-quality cannabis products, proudly ... part-time role operates under the direct, on-premises personal supervision of a licensed Pharmacist ...

Pharmacist Intern (Part-time)

Richmond, VA · On-site

$16.50 - $20.50/hr

We cultivate, manufacture, and sell a broad portfolio of high-quality cannabis products, proudly ... part-time role operates under the direct, on-premises personal supervision of a licensed Pharmacist ...

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Staff Pharmacist

Houston, TX · On-site

$50 - $60/hr

Employment Type: Part-Time Address: 7515 S. Main St., Houston, TX 77030 Website: www ... Scripts Rx is a fast-growing, specialty pharmacy company that helps patients and drug manufacturers ...

Past experience in a highly regulated field producing pharmaceutical or nutraceutical products ... Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or ...

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Job Summary We are seeking a part-time Staff Pharmacist with hands-on non-sterile compounding ... Counsel patients on both commercially manufactured and compounded medications, including usage ...

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Part Time Pharmaceutical Manufacturing information

See salary details

$18

$27

$40

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

As of Jun 12, 2026, the average hourly pay for part 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 are some common responsibilities and challenges faced by part-time employees in pharmaceutical manufacturing roles?

Part-time employees in pharmaceutical manufacturing typically assist with tasks such as operating equipment, maintaining cleanliness, packaging products, and supporting quality control processes. One common challenge is adapting to varying shifts and quickly learning standard operating procedures to ensure product safety and regulatory compliance. Since part-time roles often involve working alongside full-time staff, strong communication and teamwork skills are essential for smooth handovers and collaboration. Additionally, attention to detail is crucial, as the industry is highly regulated and even minor errors can have significant consequences.

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

To excel in a Part Time Pharmaceutical Manufacturing role, you need a basic understanding of Good Manufacturing Practices (GMP), attention to detail, and a high school diploma or equivalent. Familiarity with production equipment, batch record systems, and sometimes certifications like GMP training are typically required. Strong teamwork, reliability, and effective communication are essential soft skills in this environment. These abilities ensure adherence to quality standards, efficient production processes, and the safety of both products and personnel.

What are part time pharmaceutical manufacturing jobs?

Part time pharmaceutical manufacturing jobs involve working in the production or packaging of medications and related products, but on a reduced hours schedule compared to full-time roles. These positions support various stages of the manufacturing process, such as operating equipment, quality control, and maintaining safety standards. Part time roles can appeal to students, parents, or individuals seeking flexible work hours, and usually require attention to detail, good organizational skills, and adherence to strict regulations. The responsibilities and required qualifications may vary depending on the employer and specific position within the manufacturing process.

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

AspectPart Time Pharmaceutical ManufacturingPart Time Pharmaceutical Quality Control
CredentialsHigh school diploma or equivalent; technical training often preferredHigh school diploma or equivalent; laboratory or quality assurance training beneficial
Work EnvironmentManufacturing plants, production linesLaboratories, testing facilities
Industry UsageProduction of pharmaceutical productsInspection, testing, and ensuring product quality
Common Search IntentManufacturing roles, production jobsQuality assurance, testing positions

Part Time Pharmaceutical Manufacturing involves working on the production line to create medications, focusing on assembly and packaging. In contrast, Part Time Pharmaceutical Quality Control emphasizes testing and inspecting products to ensure they meet quality standards. Both roles are essential in the pharmaceutical industry and often require similar certifications, but they focus on different stages of the manufacturing process.

What cities are hiring for Part Time Pharmaceutical Manufacturing jobs? Cities with the most Part 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:

Document Specialist (Part-TIme)

Ursitti Enterprises LLC

Portage, IN

$19 - $20/hr

Part-time

Posted yesterday


Job description

Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their Portage Facility! If you meet the qualifications below, APPLY NOW!

$20.00/Hour


Job Description:

We seek a meticulous and organized Document Specialist to join our client's team in Portage. As a Document Specialist, you will be crucial in managing and maintaining various documents critical to their operations, including regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other essential records.

Responsibilities:

  • Document Management: Ensure the accurate and timely creation, revision, and maintenance of documents, adhering to established guidelines and regulatory requirements.
  • Quality Control: Perform thorough quality checks on documents to ensure accuracy, consistency, and compliance with internal standards and regulatory guidelines.
  • Document Review: Review documents for completeness, correctness, and clarity, collaborating with relevant stakeholders to address discrepancies or issues.
  • Version Control: Manage document versions effectively, maintaining a clear and organized version history to facilitate tracking and retrieval.
  • Documentation Support: Support various departments by assisting in preparing, formatting, and distributing documents as needed.
  • Training and Compliance: Assist in training employees on document management processes and procedures to ensure compliance with company policies and regulatory standards.
  • Continuous Improvement: Identify opportunities for process improvements and efficiency enhancements within the document management system.

Qualifications:

  • Bachelor's degree or equivalent experience in a relevant field of life sciences, business administration, or related discipline).
  • Previous experience in document management, preferably within the pharmaceutical or healthcare industry.
  • Strong attention to detail and excellent organizational skills, with the ability to effectively manage multiple tasks and priorities.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and document management software.
  • Familiarity with regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GCP, GMP) preferred.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.