What are the responsibilities and job description for the Process Technician position at Piramal Group?
Business: Pharma Solution
Department: Operations
Location: Lexington
Job Overview
The primary purpose of the role is to support the Operations team with documentation and processes to meet production needs.
Reporting Structure
Reports to Manufacturing Manager
Key Responsibilities
- Assist engineers in developing, building, or testing prototypes/new products, processes, validations or procedures.
- Adhere to all applicable regulations, policies, and procedures for health, safety and environmental compliance Monitor and adjust production processes or equipment for quality and productivity gains.
- Provide training to operators as needed
- Assist in providing information to Transfer Tech and Validation Crew on investigations
- Assist/Support OPS Management and QA: Open, Follow up, and close deviations, CAPAs, QA Investigations and TA’s.
- Assist work team in the achievement of goals/commitments and achieves own goals/commitments regardless of obstacles
- Update Operation’s SOP’s, as needed, and perform periodic review of procedures.
- Assist in driving continuous improvement activities
Education
- High School education or equivalent
Experience
- At least 2 years working within a manufacturing environment, cGMP/pharmaceutical manufacturing preferred
- Operational capacity working with batch records
- Experience with technical writing
Competencies
- Demonstrated ability to work collaboratively with others
- Excellent oral/written communications
- Skilled at conflict resolution and decision making
- Ability to read and follow written instructions, keen attention to detail
- Excellent organizational skills and ability to multi-task
Department: Operations
Location: Lexington
Job Overview
The primary purpose of the role is to support the Operations team with documentation and processes to meet production needs.
Reporting Structure
Reports to Manufacturing Manager
Key Responsibilities
- Assist engineers in developing, building, or testing prototypes/new products, processes, validations or procedures.
- Adhere to all applicable regulations, policies, and procedures for health, safety and environmental compliance Monitor and adjust production processes or equipment for quality and productivity gains.
- Provide training to operators as needed
- Assist in providing information to Transfer Tech and Validation Crew on investigations
- Assist/Support OPS Management and QA: Open, Follow up, and close deviations, CAPAs, QA Investigations and TA’s.
- Assist work team in the achievement of goals/commitments and achieves own goals/commitments regardless of obstacles
- Update Operation’s SOP’s, as needed, and perform periodic review of procedures.
- Assist in driving continuous improvement activities
Education
- High School education or equivalent
Experience
- At least 2 years working within a manufacturing environment, cGMP/pharmaceutical manufacturing preferred
- Operational capacity working with batch records
- Experience with technical writing
Competencies
- Demonstrated ability to work collaboratively with others
- Excellent oral/written communications
- Skilled at conflict resolution and decision making
- Ability to read and follow written instructions, keen attention to detail
- Excellent organizational skills and ability to multi-task
