Join to apply for the QA Technician role at Piramal Pharma Ltd
4 days ago Be among the first 25 applicants
Join to apply for the QA Technician role at Piramal Pharma Ltd
Get AI-powered advice on this job and more exclusive features.
* Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
* Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
* Identify and escalate any identified cGMP areas of concern.
* Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
* Participate in the audits of suppliers, production and support functions as required.
* Be involved in the preparation for MHRA/FDA and other regulatory body audits.
* Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
* Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
* Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied.
* Good communication skills, both verbal and written
* Good organisation skills
* Ability to work effectively individually and as part of a team
* Ability to analyse data and information to make considered decisions
* The ability to identify root cause of problems to determine appropriate solutions
* Ability to prioritise workload to ensure timelines are met
* Ability to follow instruction accurately
* Ability to escalate issues as appropriate
Job Description
Key Roles and Responsibilities:-
* Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
* Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
* Identify and escalate any identified cGMP areas of concern.
* Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
* Participate in the audits of suppliers, production and support functions as required.
* Be involved in the preparation for MHRA/FDA and other regulatory body audits.
* Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
* Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
* Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied.
Competencies:-
* Attention to detail
* Good communication skills, both verbal and written
* Good organisation skills
* Ability to work effectively individually and as part of a team
* Ability to analyse data and information to make considered decisions
* The ability to identify root cause of problems to determine appropriate solutions
* Ability to prioritise workload to ensure timelines are met
* Ability to follow instruction accurately
* Ability to escalate issues as appropriate
Qualifications
Essential Qualifications:-
* BSc in a relevant Scientific discipline or equivalent.
Essential Experience:-
* A minimum of 3 years’ experience within a cGMP environment manufacturing Active Pharmaceutical Ingredients is required.
* A College/University qualification in a scientific subject is required.
* Experience in dealing with quality assurance, analytical chemistry, development, and manufacturing groups is beneficial
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Piramal Pharma Ltd by 2x
Sign in to set job alerts for “Quality Assurance Technician” roles.
Quality Assurance Technician Pharma (graduates)
Grangemouth, Scotland, United Kingdom 1 month ago
Glasgow City, Scotland, United Kingdom 4 weeks ago
Livingston, Scotland, United Kingdom £28,000.00-£32,000.00 3 weeks ago
Bathgate, Scotland, United Kingdom 2 weeks ago
East Kilbride, Scotland, United Kingdom 6 hours ago
Edinburgh, Scotland, United Kingdom 2 days ago
Edinburgh, Scotland, United Kingdom 5 days ago
Stirling, Scotland, United Kingdom 1 week ago
Senior Quality Assurance Automation Engineer
Glasgow, Scotland, United Kingdom 1 week ago
Glasgow, Scotland, United Kingdom 2 weeks ago
Glasgow, Scotland, United Kingdom 1 week ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr