cGMP Associate
Clinton PA
Bottling Dept
Contract
6 Am to 6 PM
6 PM to 6 AM
$19-19.75 pay rate
Job Summary
The cGMP Associate Bottling supports manufacturing and packaging operations within a regulated medical device environment. This role involves hands-on bottling activities performed in a cleanroom setting while adhering to cGMP safety and quality requirements. The ideal candidate demonstrates strong manual dexterity attention to detail and the ability to work collaboratively while standing for extended periods.
Key Responsibilities
- Perform manual and semi-automated bottling labeling and packaging operations in compliance with cGMP and SOPs
- Operate within a cleanroom environment while following gowning hygiene and contamination-control procedures
- Conduct visual inspections to ensure product quality and accuracy
- Accurately complete batch records logbooks and production documentation
- Maintain a clean and organized work area in accordance with safety and quality standards
- Communicate effectively and work closely with cross-functional team members to meet production goals
- Follow all regulatory quality and EHS requirements during daily operations
Required Skills & Qualifications
- Strong manual dexterity and ability to perform repetitive tasks with precision
- Ability to stand for long hours and perform physically demanding work
- Comfortable working in a cleanroom environment
- Good communication skills and ability to interact effectively with team members
- Basic understanding of cGMP quality systems and regulatory requirements
- High attention to detail and commitment to compliance
Preferred Qualifications
- Prior experience in the medical device industry
- Experience in bottling packaging or manufacturing operations in regulated environments (pharma biotech food or similar industries)
- Familiarity with FDA regulations and quality documentation practices
Work Environment
- Cleanroom manufacturing setting
- Requires prolonged standing repetitive hand movements and use of PPE
cGMP Associate Clinton PA Bottling Dept Contract 6 Am to 6 PM 6 PM to 6 AM $19-19.75 pay rate Job Summary The cGMP Associate Bottling supports manufacturing and packaging operations within a regulated medical device environment. This role involves hands-on bottling activities performed in a cl...
cGMP Associate
Clinton PA
Bottling Dept
Contract
6 Am to 6 PM
6 PM to 6 AM
$19-19.75 pay rate
Job Summary
The cGMP Associate Bottling supports manufacturing and packaging operations within a regulated medical device environment. This role involves hands-on bottling activities performed in a cleanroom setting while adhering to cGMP safety and quality requirements. The ideal candidate demonstrates strong manual dexterity attention to detail and the ability to work collaboratively while standing for extended periods.
Key Responsibilities
- Perform manual and semi-automated bottling labeling and packaging operations in compliance with cGMP and SOPs
- Operate within a cleanroom environment while following gowning hygiene and contamination-control procedures
- Conduct visual inspections to ensure product quality and accuracy
- Accurately complete batch records logbooks and production documentation
- Maintain a clean and organized work area in accordance with safety and quality standards
- Communicate effectively and work closely with cross-functional team members to meet production goals
- Follow all regulatory quality and EHS requirements during daily operations
Required Skills & Qualifications
- Strong manual dexterity and ability to perform repetitive tasks with precision
- Ability to stand for long hours and perform physically demanding work
- Comfortable working in a cleanroom environment
- Good communication skills and ability to interact effectively with team members
- Basic understanding of cGMP quality systems and regulatory requirements
- High attention to detail and commitment to compliance
Preferred Qualifications
- Prior experience in the medical device industry
- Experience in bottling packaging or manufacturing operations in regulated environments (pharma biotech food or similar industries)
- Familiarity with FDA regulations and quality documentation practices
Work Environment
- Cleanroom manufacturing setting
- Requires prolonged standing repetitive hand movements and use of PPE
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