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Gmp Pharmaceuticals Jobs (NOW HIRING)

ICON

GMP Equipment Validation Specialist

Lenexa, KS · On-site

As a GMP Equipment Validation Specialist at ICON you will be responsible for the ongoing qualification of equipment and controlled environments supporting 2 GMP pharmacies and a QC Laboratory. This ...

Careers at RK Pharma Inc.

GMP Cleaning

Pearl River, NY · On-site

$18 - $22/hr

RK Pharma Inc. is hiring Cleanroom Technicians to support GMP cleaning , cleanroom sanitation , and visual inspection in our pharmaceutical manufacturing facility. This role is essential to ...

GMP Pros

GMP Pros General Application

Omaha, NE · On-site

$91K - $125K/yr

At GMP Pros, Inc., we're not here to do things the way they've always been done. We're here to ... Join an innovative, fast-growing company supporting the world's top pharmaceutical, medical device ...

GMP Pros

GMP Pros General Application

Omaha, NE · On-site

At GMP Pros, Inc. ® , we're not here to do things the way they've always been done. We're here to ... Join an innovative, fast-growing company supporting the world's top pharmaceutical, medical device ...

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How much do gmp pharmaceuticals jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for gmp pharmaceuticals in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $25.72 per hour, depending on experience, location, and employer.

What are some common challenges faced in GMP Pharmaceuticals roles, and how can new employees best prepare for them?

One common challenge in GMP pharmaceutical roles is maintaining strict compliance with regulatory standards while meeting production targets. Employees must pay close attention to detailed protocols, documentation, and quality checks, as even small errors can have significant consequences. New staff can best prepare by familiarizing themselves with GMP guidelines, actively participating in training sessions, and developing strong organization and communication skills to work efficiently within cross-functional teams. Staying proactive about continuous learning and adhering to established procedures is key to success in this environment.

What are the key skills and qualifications needed to thrive in a GMP Pharmaceuticals role?

To thrive in a GMP Pharmaceuticals role, you need a strong background in pharmaceutical sciences, quality control, and regulatory compliance, often supported by a degree in pharmacy, chemistry, or related fields. Familiarity with Good Manufacturing Practice (GMP) guidelines, laboratory information management systems (LIMS), and relevant certifications such as GMP or ISO is typically required. Attention to detail, strong organizational skills, and effective team communication are crucial soft skills in this field. These skills ensure product safety, regulatory adherence, and efficient operations in pharmaceutical manufacturing environments.

What is GMP Pharmaceuticals?

GMP Pharmaceuticals are companies that manufacture pharmaceutical products in compliance with Good Manufacturing Practice (GMP) regulations. These regulations are standards set by health authorities to ensure the quality, safety, and efficacy of medicines and supplements. GMP covers all aspects of the production process, from raw material sourcing and facility hygiene to staff training and product packaging. By adhering to GMP guidelines, pharmaceutical companies help guarantee that consumers receive products that are consistently high in quality and free from contamination or errors.

What is the difference between Gmp Pharmaceuticals vs Pharmaceutical Quality Control Analyst?

AspectGmp PharmaceuticalsPharmaceutical Quality Control Analyst
CertificationsGMP certification, relevant pharmaceutical trainingGMP certification, laboratory skills certification
Work EnvironmentManufacturing facilities, quality assurance labsLaboratories, quality testing environments
Industry UsageManufacturing, quality assurance in pharmaQuality testing, analysis, and validation

Gmp Pharmaceuticals professionals focus on ensuring manufacturing processes comply with GMP standards, overseeing production quality. Pharmaceutical Quality Control Analysts primarily perform laboratory testing and analysis to verify product quality. Both roles require GMP knowledge and are integral to pharmaceutical manufacturing, but Gmp Pharmaceuticals roles are broader, encompassing production oversight, while Quality Control Analysts focus on testing and data analysis.

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Gmp Pharmaceuticals jobs near you
Infographic showing various Gmp Pharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Nights. Highlights an 100% In-person job distribution, with an average salary of $47,496 per year, or $22.8 per hour.

Senior GMP Equipment Technician

Frontage Laboratories

Exton, PA • On-site

Full-time

Medical, Dental, Life, Retirement

Re-posted 10 days ago

Job description

Senior GMP Equipment Technician

Title: Senior GMP Equipment Technician

Location: Exton, PA

Full-time

Frontage Laboratories:

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position/Job Summary:

We are seeking a highly hands-on Senior Equipment Technician to support the installation, maintenance, troubleshooting, and emergency repair of GMP pharmaceutical manufacturing equipment used in Sterile and non-sterile dosage manufacturing operations within a GMP-regulated, ISO-classified cleanroom environment.

This role is ideal for an experienced maintenance professional who enjoys working directly on equipment, solving mechanical and electrical problems, and responding quickly to critical manufacturing issues in a GMP-regulated environment.

Roles & Responsibilities:

Equipment Installation & Setup

  • Lead installation, setup, and commissioning of GMP manufacturing equipment, including FAT/SAT (Factory/Site Acceptance Testing) and IQ/OQ support.
  • Support equipment startup, change parts setup, alignment, calibration, and mechanical adjustments.
  • Execute and document annual calibration, preventive maintenance (PM), and emergency repairs on production machinery.
  • Coordinate with OEM vendors during major installations and repairs.
  • Perform hands-on preventive maintenance (PM), corrective maintenance, and emergency troubleshooting on pharmaceutical manufacturing equipment.
  • Rapidly diagnose and repair mechanical, electrical, pneumatic, hydraulic, and automation-related equipment failures.
  • Support on-call and off-shift emergency maintenance activities when required.
  • Minimize equipment downtime and restore manufacturing operations safely and efficiently.
  • Complete maintenance documentation, work orders, logbooks, and calibration records accurately.
  • Ensure all work complies with cGMP, safety, and company procedures.
  • Support deviation investigations and corrective actions related to equipment issues.
  • Maintain equipment in inspection-ready condition.
  • Identify recurring equipment problems and recommend reliability improvements.
  • Support spare parts inventory and preventive maintenance optimization.
  • Assist in equipment upgrades and process improvement projects.

Required Equipment Experience

  • Hands-on experience maintaining and troubleshooting pharmaceutical manufacturing equipment such as, Rotary tablet press, Fluid bed dryer/coater, Encapsulator, High shear granulator, Blender, Mixer, Aseptic filling line, Lyophilizer, Packaging line, CIP/SIP system, HVAC and clean utility system.
  • Experience with OEM equipment such as Fette, Korsch, Bosch, IMA, Glatt, GEA, MG2, or similar equipment is strongly preferred.

Qualifications

  • Technical school certification, technical training, or equivalent hands-on maintenance experience preferred.
  • 5+ years of hands-on maintenance experience in pharmaceutical, biotech, or GMP-regulated manufacturing.
  • Experience with electrical systems, motors, sensors, PLCs, and automation troubleshooting is highly desirable.
  • Ability to read mechanical drawings, wiring diagrams, and equipment manuals.
  • Experience working in cleanroom and GMP manufacturing environments preferred.

Required Skills

  • Strong hands-on mechanical aptitude.
  • Emergency troubleshooting and repair capability.
  • Familiarity with GMP documentation practices.
  • Ability to work independently with minimal supervision.
  • Strong sense of urgency and ownership.
  • Ability to lift equipment/heavy parts/tools and work around manufacturing equipment.
  • Ability to work in cleanroom and gowning environments.
  • May require weekend, overtime, or on-call support during critical operations.
  • Ability to stand and work on the manufacturing floor for extended periods.

Salary and Benefits:

Frontage Laboratories offer a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.