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13 days ago
Piramal Pharma·Pharma·13 days ago
13 days ago

Pharmaceutical Process Operator

Mid · 2-5 years

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About this role

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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

Pharmaceutical Process Operator

Job Description

Job Summary:**

Piramal Pharma Solutions - Morpeth is seeking a dedicated Pharmaceutical Process Operator to execute and monitor manufacturing processes for pharmaceutical products, ensuring adherence to quality standards and safety protocols.

Job Responsibilities:**

* Operate, monitor, and troubleshoot production equipment according to Standard Operating Procedures (SOPs) and batch records.
* Perform in-process checks and document all manufacturing activities accurately and thoroughly.
* Clean and sanitize production equipment and facilities in compliance with Good Manufacturing Practices (GMP).
* Identify and report equipment malfunctions, deviations, and quality issues to supervisors.
* Follow all safety regulations and participate in safety training programs.
* Collaborate with team members to optimize production efficiency and quality.
* Maintain a clean and organized work environment.

Job Qualifications:**

* Some experience in a pharmaceutical manufacturing environment, or a related regulated industry is preferable but not required.
* Familiarity with GMP and other regulatory guidelines.
* Ability to read and interpret technical documents, including SOPs and batch records.
* Strong attention to detail and accuracy in documentation.
* Basic mathematical skills for calculations and measurements.
* Excellent communication and teamwork skills.
* Proficiency in basic computer applications.

Good Manufacturing Practices (GMP), Standard Operating Procedure (SOP)
PharmaH1B sponsor likely
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