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Pharmaceutical Manufacturing Tablet Jobs (NOW HIRING)

Pharmaceutical Manufacturing Benefits: * Competitive compensation * Health, Dental & Vision ... Hands-on experience with pharmaceutical equipment such as Fette tablet presses, MG2 encapsulation ...

Production Operator

Chantilly, VA · On-site

$47K - $70K/yr

Hands-on experience in Oral Solid Dosage (OSD) manufacturing. * Proficiency in set-up, operation, and cleaning of pharmaceutical equipment (e.g., tablet press, encapsulation, coating systems)

Manufacturing Intern

Myerstown, PA · On-site

$24 - $43.25/hr

Learn the basics of pharmaceutical Manufacturing and Packaging processing and equipment including dispensing, mixing, wet granulation, tablet compression, coating, and tablet printing; Be able to ...

Manufacturing Intern

Myerstown, PA · On-site

$24 - $43.25/hr

Learn the basics of pharmaceutical Manufacturing and Packaging processing and equipment including dispensing, mixing, wet granulation, tablet compression, coating, and tablet printing; * Be able to ...

Learn the basics of pharmaceutical Manufacturing and Packaging processing and equipment including dispensing, mixing, wet granulation, tablet compression, coating, and tablet printing; * Be able to ...

Manufacturing Intern

Myerstown, PA · On-site

$24 - $43.25/hr

Learn the basics of pharmaceutical Manufacturing and Packaging processing and equipment including dispensing, mixing, wet granulation, tablet compression, coating, and tablet printing; * Be able to ...

Learn the basics of pharmaceutical Manufacturing and Packaging processing and equipment including dispensing, mixing, wet granulation, tablet compression, coating, and tablet printing; * Be able to ...

Showing results 21-40

Pharmaceutical Manufacturing Tablet information

See salary details

$14

$19

$25

How much do pharmaceutical manufacturing tablet jobs pay per hour?

As of Sep 10, 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.

Senior Production Operator - OSD Pharma Tablet Compression

Middletown, DE

WuXi AppTec
Health Care and Social Assistance

$15.75 - $19/hr

Full-time

Re-posted 6 days ago


Key responsibilities

  • Execute manufacturing steps per approved batch records and record results contemporaneously.

  • Set up, operate, and monitor designated equipment within validated parameters, and support changeovers to minimize downtime.

  • Complete batch records, logbooks, and forms accurately, and support investigations and audits related to deviations or atypical events.


Job description

Operator I supports cGMP pharmaceutical manufacturing activities by executing batch operations, cleaning and setup, in-process checks, and documentation with a strong focus on safety, quality, and right-first-time performance. This role is fully trained to operate designated equipment and to work effectively within a cross-functional team in a regulated environment.

This job is at our new, state-of-the-art OSD plant in Middletown, DE.  Relocation assistance will be considered.  


Production Operations
  • Perform manufacturing steps per approved batch records (e.g., dispensing, measuring, charging, mixing, filtration, filling, capping, packaging etc.) and record results contemporaneously.
  • Set up, operate, and monitor assigned equipment (e.g., tablet presses, roller compactors, etc.) within validated parameters.
  • Conduct and document in-process checks (pH, weight/volume, torque, visual inspection etc.) and make routine adjustments under supervision.
  • Execute line clearances and support changeovers, including equipment assembly and disassembly between production batch runs to minimize downtime.
  • Work in classified areas (ISO 8–7) following aseptic techniques and environmental monitoring practices.
  • Complete initial and periodic gowning qualifications; perform routine interventions per procedure.
  • Perform equipment and area cleaning (CIP/SIP/manual) and document to meet cleanliness status/line clearance.
  • Assist with basic troubleshooting; partner with Maintenance/Engineering for repairs and PMs.

Documentation & Quality

  • Complete batch records, logbooks, and forms accurately and legibly; reconcile materials and yields.
  • Initiate notifications for deviations, OOS/OOT, or atypical events; support investigations and CAPAs as needed.
  • Participate in audits, room/equipment release, and lot sampling activities.
  • Meet or exceed KPIs (Right-First-Time, schedule adherence, yield, 5S audit scores etc.).
  • Suggest and help implement process and documentation improvements (lean, 5S, SMED).
  • Collaborate with QA, QC, MSAT/Process Engineering, Supply Chain, Facilities, and EHS.

  • Bachelor’s or technical certificate in a science/technical field preferred.
  • Experience working with tablet presses, encapsulators, fluid bed dryers, roller compactors, blenders, coaters and/or other pharmaceutical manufacturing equipment is required.
  • Minimum of 3 years in GMP manufacturing, food/beverage, biotech, medical device, or similar regulated/industrial setting preferred (new-grad friendly).
  • Experience assisting in regulatory inspections and audits.
  • Ability to work in a fast-paced, highly regulated environment. 

Knowledge / Skills / Abilities:

  • Fundamental understanding of cGMPs, cleanroom behaviors, and data-integrity expectations.
  • Ability to learn and operate production equipment and read P&IDs, batch records, and SOPs.
  • Basic math and measurement skills; able to use scales, pH meters, and hand tools.
  • Computer literacy; experience with MES/LIMS/ERP and electronic logbooks a plus.

Physical & Work Environment Requirements:
• Stand/walk for extended periods (8–12 hour shifts); lift/push/pull up to 50 lbs.
• Work in controlled environments; wear PPE (gowning, gloves, safety glasses, face coverings, hearing protection as applicable).
• Exposure to chemicals, sanitizers/disinfectants, and routine noise levels within regulated limits

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.