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Pharmaceutical Manufacturing Tablet Jobs (NOW HIRING)

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Production Operator II / III

Cranbury, NJ · On-site

$20 - $26/hr

Pharmaceutical Manufacturing - Oral Solid Dosage. We are seeking an experienced Production Operator II / III with hands-on experience in oral solid dosage/tablet pharmaceutical manufacturing within a ...

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Pharmaceutical Manufacturing Tablet information

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How much do pharmaceutical manufacturing tablet jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for pharmaceutical manufacturing tablet in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a pharmaceutical manufacturing tablet operator?

Pharmaceutical manufacturing tablet operators are professionals responsible for running machines that produce tablets, such as pills or capsules, in pharmaceutical manufacturing facilities. They oversee the tablet press machines, ensure the correct formulation and quality of the product, and monitor the production process for efficiency and safety. Operators also conduct routine maintenance on equipment, perform quality checks, and follow strict regulatory guidelines to ensure the tablets meet industry standards. Their work is crucial in ensuring that medications are produced safely and consistently.

What are the key skills and qualifications needed to thrive as a pharmaceutical manufacturing tablet operator?

To thrive as a Pharmaceutical Manufacturing Tablet Operator, you need a solid understanding of GMP (Good Manufacturing Practices), quality control, and basic mechanical skills, usually supported by a high school diploma or associate degree in a relevant field. Familiarity with manufacturing equipment, tablet press machines, and electronic batch record systems is typically required, along with any necessary safety certifications. Attention to detail, problem-solving abilities, and strong teamwork help operators maintain product quality and safety standards. These skills and qualities are essential for ensuring consistent production, regulatory compliance, and the safe delivery of pharmaceutical products.

What are some common challenges faced by professionals working in pharmaceutical tablet manufacturing?

Professionals in pharmaceutical tablet manufacturing often encounter challenges such as maintaining strict quality standards, adhering to Good Manufacturing Practices (GMP), and managing documentation for regulatory compliance. There can also be difficulties in troubleshooting equipment malfunctions or process deviations, which require quick problem-solving skills. Additionally, working as part of a cross-functional team—often with engineers, quality assurance, and research staff—means effective communication and collaboration are essential for timely and accurate production.

What is the difference between Pharmaceutical Manufacturing Tablet vs Pharmaceutical Manufacturing Capsule?

AspectPharmaceutical Manufacturing TabletPharmaceutical Manufacturing Capsule
Required CredentialsTypically requires GMP training, technical skills, and sometimes certifications in pharmaceutical manufacturingSimilar credentials as tablets, including GMP compliance and technical knowledge
Work EnvironmentManufacturing plants, cleanrooms, production linesSimilar manufacturing environments, often in the same facilities
Employer & Industry UsagePharmaceutical companies producing solid oral dosage formsSame industry, producing capsules as alternative dosage forms
Common Search & Comparison IntentUnderstanding roles in tablet productionUnderstanding roles in capsule production

Both pharmaceutical manufacturing tablets and capsules involve similar skills, certifications, and work environments. The main difference lies in the dosage form produced: tablets are compressed solid forms, while capsules are filled containers. Professionals in both roles often work in the same facilities and require comparable qualifications, but their specific tasks focus on different product types.

What are popular job titles related to Pharmaceutical Manufacturing Tablet jobs?

For Pharmaceutical Manufacturing Tablet jobs, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Manufacturing Tablet job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Manufacturing Operations Manager (Tablet manufacturing)

Pittsburg, CA • On-site

Nivagen Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees
Learn more about Nivagen Pharmaceuticalsexternal

Full-time

Re-posted 15 days ago

Job description

Company
Nivagen pharmaceuticals Inc. located in Sacramento CA, we are engaged in the development, acquisition and sales of generic prescription drugs and over the counter products for the North American market. Our vision is to deliver high-quality products at affordable prices by leveraging global partnerships with the best FDA approved manufacturing facilities across the world.
Nivagen is focused in three areas of product development: development/co-development, acquisition/in-licensing, and providing sales and marketing services.
Role Purpose:
Responsible for performing tasks to specifications related to oral solid pharmaceutical manufacturing. The process includes tablet manufacturing.
Key Duties & Responsibilities:
  • Responsible for hands-on operation of production equipment including but not limited to: Blenders, Tablet Press, High Shear Granulator, Tray Dryer, Fluid Bed Processing Units, Mixers, Pumps, Vacuum and Loading machines, Labeling machines, Imprinting machines, Sealers, Bottle filling machines, Cappers, Induction sealers as Production Supervisor / Team Lead to manufacture oral dosage forms in a cGMP manufacturing facility.
  • Draft and manage daily/weekly production schedule
  • Ensure compliance with regulatory requirements such as Good Manufacturing Practices (GMP), Occupational Safety and Health Administration (OSHA) guidelines, and Environmental Health and Safety (EHS) regulations. You will stay updated with industry regulations and implement necessary changes to maintain compliance.
  • Manage workload of all the technicians and support staff in various departments such as mixing, granulation, drying, blending, compression, coating, packaging, receiving and warehouse.
  • Coordinate with relevant functional groups to ensure adherence to the production protocol and target volume requirements. Collaborate with cross-functional teams, such as R&D, engineering, and quality control, to support product launches, process validations, and technology transfers.
  • Troubleshoot and investigate deviations, actively participate in process optimization, support QA and other functional groups during internal and external audits including FDA, and actively support change control process.
  • Draft SOPs, training manual, qualification documents, protocols, and other controlled documents.
  • Manage receiving and warehouse personnel, inventory management, and ordering of supplies.
  • Performs all job duties in compliance with current Good Manufacturing Practices (cGMPs), following Nivagen Pharmaceuticals Quality Manual and Facility Standard Operating Procedures (SOPs).
  • Records all pertinent operations in packaging records, logbooks, and controlled documents.
  • Performs assembly, disassembly, operation, and cleaning of production and equipment.
  • Assists in routine preventive maintenance of all the utilities, production and packaging equipment.
  • Cleans and maintains production environments.
  • Performs line clearances prior to initiation of production orders to ensure materials and documents pertaining to the previous order have been appropriately removed from the production area.
  • Promote a culture of continuous improvement by encouraging suggestions and ideas from the team, implementing best practices, and monitoring key performance indicators (KPIs) to drive operational excellence.

Education
  • Requires Bachelor's Degree with 5 to 10 years in the pharma/Nutraceutical/Supplement environment
  • Requires experience with and an in-depth knowledge of cGMP regulatory requirements as they relate to the production of pharmaceutical products
  • Must be able to operate pharmaceutical manufacturing machinery
  • Solid mechanical aptitude and troubleshooting skills
  • Must have excellent communication skills
  • Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements, GMP
  • 5 to 10 years in Pharmaceuticals production

Technical competencies
  • Excellent written and verbal communication skills
  • Excellent math skills
  • Ability to read and comprehend SOP's, Batch Records and training documents.
  • Ability to multi-task effectively
  • Excellent interpersonal skills and ability to effectively interact with different functional groups

Apply