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Weekend Pharmaceutical Manufacturing Jobs in Texas

Sterile Manufacturing Operator

Houston, TX · On-site

$16.75 - $20/hr

As the nation's most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility, we're redefining what's possible in personalized medicine and pharmaceutical manufacturing. We're ...

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Weekend Pharmaceutical Manufacturing information

What is a weekend pharmaceutical manufacturing job?

A Weekend Pharmaceutical Manufacturing job involves working in a facility that produces pharmaceutical products, such as medications or vaccines, primarily during the weekend shifts. Employees in this role are responsible for operating machinery, monitoring production processes, ensuring quality control, and adhering to safety and regulatory standards. Weekend shifts are often offered to maintain continuous production and may appeal to those seeking flexible or part-time schedules. These positions typically require attention to detail, the ability to follow strict protocols, and sometimes experience or training in manufacturing or pharmaceuticals.

What are the key skills and qualifications needed to thrive as a weekend pharmaceutical manufacturing professional?

To thrive in Weekend Pharmaceutical Manufacturing, you need a solid understanding of Good Manufacturing Practices (GMP), attention to detail, and a high school diploma or relevant technical certification. Familiarity with manufacturing equipment, batch record systems, and safety protocols is essential, often supported by on-the-job training or certifications like OSHA. Strong teamwork, reliability, and effective communication are vital soft skills for ensuring smooth operations during off-peak hours. These skills and qualities are crucial for maintaining production quality, safety, and efficiency in a highly regulated environment.

What are some common challenges faced in a weekend pharmaceutical manufacturing role, and how can they be managed?

One common challenge in weekend pharmaceutical manufacturing is maintaining consistent communication with weekday teams, as production must remain seamless across shifts. Additionally, weekend staff may encounter unexpected equipment issues or deviations with limited on-site support. Proactively documenting processes, participating in thorough shift handovers, and utilizing digital communication tools can help address these challenges. Staying adaptable and resourceful is important, as weekend teams often take on broader responsibilities to ensure production targets and quality standards are met.

What is the difference between Weekend Pharmaceutical Manufacturing vs Weekend Pharmaceutical Packaging?

AspectWeekend Pharmaceutical ManufacturingWeekend Pharmaceutical Packaging
CertificationsPharmaceutical manufacturing certifications, GMP trainingPackaging certifications, GMP training
Work EnvironmentProduction floors, manufacturing labsPackaging lines, labeling areas
Job FocusProducing active ingredients, formulationAssembling, labeling, and packaging products
Industry UsageManufacturing plants, pharmaceutical companiesPackaging facilities, pharmaceutical companies

Weekend Pharmaceutical Manufacturing involves producing drugs and active ingredients, focusing on formulation and production processes. In contrast, Weekend Pharmaceutical Packaging centers on preparing finished products for distribution, including labeling and packaging tasks. Both roles require GMP training and are essential in pharmaceutical production, but they differ in daily tasks and work environment.

What are the most commonly searched types of Pharmaceutical Manufacturing jobs in Texas?

The most popular types of Pharmaceutical Manufacturing jobs in Texas are:

What cities in Texas are hiring for Weekend Pharmaceutical Manufacturing jobs?

Cities in Texas with the most Weekend Pharmaceutical Manufacturing job openings:

Solid Dose Manufacturing Technician

Sovereign Pharmaceuticals

Fort Worth, TX • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

SUMMARY/OBJECTIVE
The Solid Manufacturing Technician I is an entry-level role responsible for supporting the manufacturing of solid-dose pharmaceutical products, including granulation, blending, compression, encapsulation, and coating. The technician performs cleaning, equipment setup, material handling, and basic operation under direct supervision. This position ensures all activities follow cGMP requirements, SOPs, and safety standards to support consistent product quality and efficient production flow.

ESSENTIAL FUNCTIONS

Equipment Preparation & Operation

  • Learns to operate and monitor solid-dose manufacturing equipment, including:
    • Granulators, blenders, oscillators, Fitzmill/Comill systems
    • Tablet presses (e.g., Kikusui Libra, Gemini, Rotapress, Nova)
    • Encapsulation equipment
    • Tablet coating equipment (e.g., coating pans, spray systems)
    • Dedusters, metal detectors, hardness testers, thickness gauges and scales
  • Assists in assembling, disassembling, and cleaning equipment according to SOPs.
  • Prepares rooms and equipment before and after manufacturing operations.
  • Assists in charging materials into equipment under supervision, including coating solutions and slurry.
  • Performs basic machine adjustments as directed to maintain product quality.

Material Handling

  • Weighs and verifies raw materials with QA present, including excipients, and APIs
  • Safely handles raw powders, granulated product, intermediates, and coating materials.
  • Ensures materials are properly labeled, stored, and staged for production.

Product Quality & Compliance

  • Follows detailed batch record steps and SOP instructions for all unit operations, including coating parameters.
  • Conducts in-process checks with guidance, such as:
    • LOD testing
    • Tablet weight, hardness, thickness, friability
    • Coating weight gain and visual appearance checks
  • Ensures all work requiring verification is checked by authorized personnel.
  • Reports deviations or abnormal conditions immediately to section lead and supervisor.

Documentation

  • Accurately documents all work in batch records, logbooks, and cleaning logs, including coating activities.
  • Records measurements, observations, and process adjustments in real time.
  • Ensures documentation complies with cGMP, GDP, and site requirements.
  • Ensures all MasterControl training requirements are completed within the required timeframe and maintains proficiency in printing SOPs, cleaning checklists, and other controlled documents.

Cleaning & Maintenance

  • Performs A, B, and S cleans of equipment and production rooms, including coating pans, spray guns, and solution tanks.
  • Assists with minor preventive maintenance under supervision.
  • Maintains clean and organized work areas to prevent contamination.

Safety Compliance

  • Follows all safety procedures and PPE requirements, including those specific to handling solvents or coating materials.
  • Reports unsafe conditions, equipment issues, or near-misses immediately to section lead and supervisor.
  • Participates in required safety training.

Troubleshooting & Reporting

  • Assists in basic troubleshooting of equipment issues across all areas, including coating systems.
  • Escalates complex mechanical or process-related concerns to senior staff.

Other Responsibilities

  • Participates in on-the-job training to progress toward independent operation in all manufacturing areas.
  • Performs additional related duties to support departmental goals

REQUIRED SKILLS/ ABILITIES

  • Ability to follow detailed written and verbal instructions.
  • Strong attention to detail and documentation accuracy.
  • Basic math and mechanical aptitude.
  • Dependable and able to work effectively in a team environment.
  • Ability to safely lift up to 50 lbs and perform extended physical activity.

REQUIRED EDUCATION AND EXPERIENCE

  • High school diploma or GED equivalent.
  • No prior pharmaceutical experience required.
  • Minimum of 1 year of experience in pharmaceutical, food, or other regulated manufacturing environments.

PREFERRED EDUCATION AND EXPERIENCE

  • Experience in manufacturing, production, or mechanical work environments.
  • Familiarity with cGMP, batch records, or regulated industry practices.
  • Experience with solid-dose equipment or mechanical systems is a plus.

position type/expected hours of work
Employment Type: Full-Time

Shift Schedule:

  • First Shift: Monday - Friday, 6:00 AM - 2:30 PM

?Flexibility for overtime or weekend work may be required.

physical demands

Ability to lift and handle up to 50 lbs frequently.

Prolonged standing, walking, bending, and reaching during operations.

Manual dexterity for equipment adjustments and coating spray components.

work environment

Pharmaceutical manufacturing environment with exposure to powders, solvents, and moving machinery.

Required PPE includes safety glasses, gloves, hearing protection, and appropriate garments.

Temperature and humidity may vary depending on processes.