Operations GMP Cleaning Specialist

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Division

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

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.

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.