What are the responsibilities and job description for the Validation Engineer Senior position at ACL Digital?
Job Details
Responsibilities:
Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
Work with project teams to develop the commissioning and qualification strategy and document in qualification plans.
Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment.
Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equipment.
Ensure that Qualification/Validation plans are generated and updated for all ongoing projects.
Prepare, evaluate and approve technical and GMP linked documentation such as URS, FMEA, impact/risk assessment, master plans, qualification/validation documentation.
Arrange and implement FAT/SAT, commissioning activities for new GMP systems in collaboration with both internal and external partners.
Other duties may be assigned to this role.
Key Skills and Requirements:
Educated to a degree level in a technical or natural scientific field.
Demonstrable experience in a pharma organization within a C&Q/CQV corresponding role.
Knowledge of qualification needs to cGMP guidelines.
Familiarity with Kneat Gx Platform or other digital C&Q systems.
Familiarity working with cross-department stakeholders.
Knowledge of quality assurance principles.
Experience working within project teams and various projects in parallel.
Prior involvement working with ISPE baseline guide vol 3, vol 4 and vol 5 would be beneficial.
Effective communication skills, both verbally and in writing.
Able to think analytically with the ability to resolve issues.
Able to manage own time efficiently.
Position could be extended to up to 3 years
Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
Work with project teams to develop the commissioning and qualification strategy and document in qualification plans.
Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment.
Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equipment.
Ensure that Qualification/Validation plans are generated and updated for all ongoing projects.
Prepare, evaluate and approve technical and GMP linked documentation such as URS, FMEA, impact/risk assessment, master plans, qualification/validation documentation.
Arrange and implement FAT/SAT, commissioning activities for new GMP systems in collaboration with both internal and external partners.
Other duties may be assigned to this role.
Key Skills and Requirements:
Educated to a degree level in a technical or natural scientific field.
Demonstrable experience in a pharma organization within a C&Q/CQV corresponding role.
Knowledge of qualification needs to cGMP guidelines.
Familiarity with Kneat Gx Platform or other digital C&Q systems.
Familiarity working with cross-department stakeholders.
Knowledge of quality assurance principles.
Experience working within project teams and various projects in parallel.
Prior involvement working with ISPE baseline guide vol 3, vol 4 and vol 5 would be beneficial.
Effective communication skills, both verbally and in writing.
Able to think analytically with the ability to resolve issues.
Able to manage own time efficiently.
Position could be extended to up to 3 years
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
