Senior Associate QA (GMP)

Location Breda, Netherlands
Discipline: Biotechnology
Contact name: Michelle Terraneo

Contact email: m.terraneo@panda-int.com
Job ref: 11133
Published: about 1 month ago
Do you want to work for a Fortune 500 company based in Breda? then keep on reading!

For our client, we are looking for a motivated QA Associate! 

Your Tasks consist of: 

- Provide QA guidance and support in the production area
- To perform batch record review of batches assembled, packaged and labeled at ABR and contract manufacturers.
- To establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person

- Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions.
- Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.
- Review and approve batch production record data entries before production activities take place
- Perform finished product checks during (commercial) production runs
- Compile and review batch records for lots assembled, packaged and labeled at ABR and contract manufacturers in preparation for disposition by QP.
- Review of operational SOP’s and Work Instructions as needed
- Review and approve deviation records
- Initiate and own QA deviations as needed.
- Perform GMP compliance checks in production
- Assist in development and delivery of GMP training activities for QA and production staff
- Participate in QA production related projects as needed
- Assist in various investigations as needed
- Assist in ABR projects and improvement efforts as needed
- Responsible for preparation of weekly/monthly metrics
- Own and maintain departmental performance boards

Knowledge
Understanding and application of principles, concepts, theories and standards of technical/scientific field
Specialized knowledge within own specialty area
Deepens technical knowledge through exposure and continuous learning
Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
Problem Solving
Applies research, information gathering, analytical and interpretation skills
to problems of diverse scope
Ensures compliance within regulatory environment
Develops solutions to technical problems of moderate complexity
Screens, categorizes, evaluates, reconciles, reports and resolves data integrity issues
Interprets generally defined practices and methods
Autonomy
Works under general direction
Work is guided by objectives of the department or assignment
Refers to technical standards, principles, theories and precedents as needed
May set project timeframes and priorities based on project objectives and ongoing assignments
Recognizes and escalates problems
Contribution
Contributes to work group/team by ensuring the quality of the tasks/services provided by self
Contributes to the completion of milestones associated with specific projects or activities within own department or workgroup
Provides training/guidance to others and acts as a technical/scientific resource within work group/team
Establishes working relationships with others outside area of expertise

Minimum Requirements

- Master’s degree in Life Sciences or related field or the equivalent combination of education and/or experience.
-Typically 3 years of related Quality Assurance or manufacturing -- --experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.
Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
Manufacturing and/or Quality analytical processes and operations.

Interested? 

Then send me your CV + Motivation and i will call you ASAP!