Technical Assistant
- Recruiter
- Confidential
- Location
- Blackpool
- Salary
- Competitive
- Posted
- 03 Jun 2021
- Closes
- 16 Jun 2021
- Sectors
- Manufacturing & Industrial
- Contract Type
- Permanent
- Hours
- Full Time
Technical Assistant
Blackpool
Competitive salary
The technical assistant will be responsible for assisting the technical director in ensuring that technical, quality assurance and departmental tasks are completed in a timely manner to support the technical director and the department as a whole in the delivery of specific pieces of work or projects.
Responsibilities of the job include:
Entering and updating raw material information and new product specifications onto the technical MRP system
Regular monitoring of approved specifications of raw materials against materials from new suppliers
Approving new raw materials and entering onto the system
Completing customer documentation or questionnaires
Developing and entering new customer formulations onto the system and issuing relevant documentation
Responding to customer enquiries giving complete and accurate information within 3 working days
Involvement in laboratory based trials for new raw materials and/or product formulations
Attend departmental meetings and training as and when required
Help investigation of customer complaints in a timely manner
Assisting technical with the generation and updating of product and raw material specifications when required
Generation of Quality Attribute Sheets that comply with customer and legal specifications and requirements
Reporting any non-conformities, via the CAPA system, taking appropriate action as necessary and documenting relevant information
Review manufacturing processes and work with the production / technical teams to improve the systems when required
Any other reasonable management request
Regulatory compliance - Label Overview and approval on the system - informing customers of any changes required
Regulatory Compliance - Pharmacovigilance overview and review - Product Quality Review.
ESSENTIAL SKILLS
Time Management
Computer Skills
Knowledge of Quality Systems and pharmaceutical working practices
Knowledge of auditing processes and procedures
DESIRABLE SKILLS
Knowledge of processes used in the manufacture of solid dosage forms and liquid formulation
Product Analysis
Validation methods
Experience/knowledge of regulatory compliance
Due to the development and changing nature of quality/technical requirements within the business it is essential that you are flexible and will carry out occasional or new tasks as required.
Due to the development and changing nature of quality/technical requirements within the business it is essential that you are flexible and will carry out occasional or new tasks as required.
If you are interested in this role and have the skills and experience required, please click 'apply now', thank you
Cordant People are an equal opportunities employer
Blackpool
Competitive salary
The technical assistant will be responsible for assisting the technical director in ensuring that technical, quality assurance and departmental tasks are completed in a timely manner to support the technical director and the department as a whole in the delivery of specific pieces of work or projects.
Responsibilities of the job include:
Entering and updating raw material information and new product specifications onto the technical MRP system
Regular monitoring of approved specifications of raw materials against materials from new suppliers
Approving new raw materials and entering onto the system
Completing customer documentation or questionnaires
Developing and entering new customer formulations onto the system and issuing relevant documentation
Responding to customer enquiries giving complete and accurate information within 3 working days
Involvement in laboratory based trials for new raw materials and/or product formulations
Attend departmental meetings and training as and when required
Help investigation of customer complaints in a timely manner
Assisting technical with the generation and updating of product and raw material specifications when required
Generation of Quality Attribute Sheets that comply with customer and legal specifications and requirements
Reporting any non-conformities, via the CAPA system, taking appropriate action as necessary and documenting relevant information
Review manufacturing processes and work with the production / technical teams to improve the systems when required
Any other reasonable management request
Regulatory compliance - Label Overview and approval on the system - informing customers of any changes required
Regulatory Compliance - Pharmacovigilance overview and review - Product Quality Review.
ESSENTIAL SKILLS
Time Management
Computer Skills
Knowledge of Quality Systems and pharmaceutical working practices
Knowledge of auditing processes and procedures
DESIRABLE SKILLS
Knowledge of processes used in the manufacture of solid dosage forms and liquid formulation
Product Analysis
Validation methods
Experience/knowledge of regulatory compliance
Due to the development and changing nature of quality/technical requirements within the business it is essential that you are flexible and will carry out occasional or new tasks as required.
Due to the development and changing nature of quality/technical requirements within the business it is essential that you are flexible and will carry out occasional or new tasks as required.
If you are interested in this role and have the skills and experience required, please click 'apply now', thank you
Cordant People are an equal opportunities employer