What are the responsibilities and job description for the QC Associate I position at Planet Pharma?
Description
Job Description
The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the RTP Drug Product site. This includes performing incoming sampling and inspections for various raw materials. The Raw Material Associate I’s responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, container closures, and packaging components, while maintaining, robust and compliant cGMP documentation practices. Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments. This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers. The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor. The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.
Pay ranges between $25-32/hr and is based on experience
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Description
The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the RTP Drug Product site. This includes performing incoming sampling and inspections for various raw materials. The Raw Material Associate I’s responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, container closures, and packaging components, while maintaining, robust and compliant cGMP documentation practices. Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments. This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers. The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor. The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.
- Must be able to move 50 lbs with assistance of equipment.
- Ability to communicate with peers and management; GMP/GDP experience
- Effective organizational skills
- Ability to multi-task and coordinate multiple activities in parallel
- Demonstrated problem solving skills
- Solid technical writing skills
Pay ranges between $25-32/hr and is based on experience
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Salary : $25 - $32
