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Evotec WD

IT Specialist III, GMP Systems

Redmond, WA · On-site

$115 - $126.50/hr

## IT Specialist III, GMP SystemsApplylocations: Redmondtime type: Full timeposted on: Posted Todayjob requisition id: JOB ID-14252**Job Title:** IT Specialist III, GMP Systems **Department:

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...

Evotec

IT Specialist III, GMP Systems

Redmond, WA · On-site

$115K - $126K/yr

Job Title: IT Specialist III, GMP Systems Department: Information Systems Location: Redmond, WA Reports to: Senior IT End User Services Manager About Us: At Just-Evotec, we believe that curiosity is ...

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How much do gmp specialist jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for gmp specialist in the United States is $23.32, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $26.44 per hour, depending on experience, location, and employer.

What is a GMP specialist?

GMP Specialists are professionals who ensure that manufacturing processes and products comply with Good Manufacturing Practice (GMP) regulations. They are responsible for developing, implementing, and monitoring quality standards in industries such as pharmaceuticals, biotechnology, and food production. Their work helps ensure that products are consistently produced and controlled according to quality standards to protect consumer safety. GMP Specialists often conduct audits, review documentation, train staff, and assist in resolving compliance issues.

What are some common challenges faced by GMP specialists when ensuring compliance in a manufacturing environment?

GMP Specialists often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation accuracy, and ensuring all staff adhere to proper procedures. They may need to address gaps in employee training, respond to audit findings, and coordinate corrective actions across multiple departments. Collaboration with quality assurance, production, and regulatory teams is crucial to maintain compliance and implement process improvements effectively.

What are the key skills and qualifications needed to thrive as a GMP specialist, and why are they important?

To thrive as a GMP Specialist, you need a thorough understanding of Good Manufacturing Practices, quality assurance protocols, and relevant scientific or engineering backgrounds, often supported by a bachelor’s degree in life sciences or a related field. Familiarity with industry-specific regulatory systems (such as FDA or EMA guidelines), laboratory information management systems (LIMS), and quality management software is crucial. Attention to detail, problem-solving abilities, and strong communication skills help ensure compliance and foster effective teamwork. These competencies are vital for maintaining product quality, regulatory adherence, and minimizing risks in pharmaceutical or biotech manufacturing environments.

What is the difference between Gmp Specialist vs Quality Assurance Associate?

AspectGmp SpecialistQuality Assurance Associate
CertificationsGMP certification, relevant industry trainingGMP training, QA certifications
Work EnvironmentManufacturing, laboratories, compliance-focused settingsQuality control labs, manufacturing sites, documentation roles
Employer & IndustryPharmaceutical, biotech, medical device companiesPharmaceutical, biotech, healthcare industries
Primary FocusEnsuring GMP compliance, documentation, and proceduresSupporting quality assurance processes, audits, and documentation

Gmp Specialists focus on maintaining GMP compliance through documentation and procedures, often working directly in manufacturing or labs. Quality Assurance Associates support QA processes, audits, and quality control activities. While both roles require GMP knowledge and certifications, Gmp Specialists typically have a more technical and compliance-oriented focus, whereas QA Associates concentrate on supporting overall quality systems.

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Gmp Specialist jobs near you
Infographic showing various Gmp Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $48,504 per year, or $23.3 per hour.

Operations GMP Cleaning Specialist

Sellersville, PA

Piramal Pharma Limited
See more jobs at Piramal Pharma Limitedexternal

Full-time

Posted 6 days ago

Job description

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Operations GMP Cleaning Specialist

Job Description

Piramal Pharma Solutions (Sellersville, PA) is seeking an Operations GMP Cleaning Specialist to support manufacturing operations by maintaining the cleanliness and organization of production areas, cleanrooms, equipment, and facility spaces in accordance with GMP requirements, company procedures, safety standards, and regulatory expectations.
The Operations GMP Cleaning Specialist will execute cleaning and sanitation activities, maintain accurate documentation, support contamination control practices, and ensure operational areas remain inspection-ready. This position may also support inventory replenishment of cleaning supplies and materials to maintain a safe and compliant work environment. Occasional evening and weekend work may be required to support business needs.

Piramal Pharma Solutions (Sellersville, PA) is seeking an Operations GMP Cleaning Specialist to support manufacturing operations by maintaining the cleanliness and organization of production areas, cleanrooms, equipment, and facility spaces in accordance with GMP requirements, company procedures, safety standards, and regulatory expectations.

The Operations GMP Cleaning Specialist will execute cleaning and sanitation activities, maintain accurate documentation, support contamination control practices, and ensure operational areas remain inspection-ready. This position may also support inventory replenishment of cleaning supplies and materials to maintain a safe and compliant work environment. Occasional evening and weekend work may be required to support business needs.

Essential Duties and Responsibilities

  • Perform cleaning and sanitation activities in accordance with approved SOPs and validated cleaning procedures.
  • Conduct and document line clearance activities before and after cleaning operations.
  • Maintain equipment and area status labels (e.g., Cleaned, To Be Cleaned, In Use).
  • Prepare, label, and manage cleaning solutions according to approved concentrations, contact times, and expiration requirements.
  • Execute cleaning activities in compliance with cleaning validation requirements and support swab and rinse sampling activities.
  • Complete all documentation in accordance with Good Documentation Practices (GDP) and ALCOA principles.
  • Initiate and support deviations, investigations, and corrective actions related to cleaning or documentation issues.
  • Follow contamination control procedures, including proper segregation of equipment and materials.
  • Adhere to cleanroom behaviors, gowning requirements, and approved cleaning techniques.
  • Maintain inspection and audit readiness and support internal and external audits as required.
  • Replenish and maintain cleaning supplies and operational consumables.
  • Follow all safety policies, procedures, and PPE requirements.
  • Perform other duties as assigned.

Education and Experience

Education

  • High School Diploma or GED required.
  • Equivalent combinations of education, training, and experience will be considered.

Experience Preferred

  • 0-1 years of commercial, industrial, pharmaceutical, GMP, or regulated-environment cleaning experience preferred.
  • Experience working in a manufacturing, pharmaceutical, or cleanroom environment is a plus.
  • Entry-level candidates with a strong work ethic and willingness to learn are encouraged to apply.

Physical Requirements

  • Ability to lift up to 40 pounds.
  • Ability to occasionally move drums weighing up to 300 pounds using appropriate equipment and safe work practices.
  • Ability to stand, walk, bend, stoop, reach, and perform repetitive movements for extended periods.
  • Ability to safely work around manufacturing equipment and cleaning chemicals.
  • Must be able to wear required Personal Protective Equipment (PPE).
  • Must not have allergies to chemicals or biological substances commonly found in manufacturing environments.

Travel Requirements

No regular travel required.

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