KAZTRONIX jobs in NEW JERSEY, United Kingdom

and packaging validation activities prior to introduction of any new or change in components/processes. Kaztronix is an equal...

validation activities prior to introduction of any new or change in components/processes. Kaztronix is an equal opportunity...

Documentation Associate Documentation Associate support the site(s) documentation system and ancillary support systems. This role will contribute to MSTG's efforts that aim to support development and validation program at Sun Pharma. The ...

Documentation Associate Documentation Associate support the site(s) documentation system and ancillary support systems. This role will contribute to MSTG's efforts that aim to support development and validation program at Sun Pharma. The ...

Training Coordinator (Onsite) Provides documentation support for all operations, related to the SOP trainings and maintains all document related Training module (LMS) to ensure regulatory compliance in accordance to 21 CFR Part 820.25 (P...

Scientist I, MSTG = Manufacturing Science and Technology Group Job Summary Scientist I performs process development studies, Exhibit batch and process qualification activities. This position also prepares technical documentation to suppo...

Scientist I, MSTG = Manufacturing Science and Technology Group Job Summary Scientist I performs process development studies, Exhibit batch and process qualification activities. This position also prepares technical documentation to suppo...

Training Coordinator (Onsite) Provides documentation support for all operations, related to the SOP trainings and maintains all document related Training module (LMS) to ensure regulatory compliance in accordance to 21 CFR Part 820.25 (P...

Contract Manufacturing Associate Job Summary Support Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality oversight. Accomplish quality objectives by planning and evaluating project a...

Contract Manufacturing Associate Job Summary Support Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality oversight. Accomplish quality objectives by planning and evaluating project a...

Compliance Associate II The Compliance Associate II is responsible for conducting activities to ensure site compliance to cGMP regulations as well as internal quality procedures. The Associate II Compliance is responsible for managing and...

Compliance Associate II The Compliance Associate II is responsible for conducting activities to ensure site compliance to cGMP regulations as well as internal quality procedures. The Associate II Compliance is responsible for managing and...

Manufacturing Operator- Raw Materials Dispensing Summary: To perform dispensing of raw materials for manufacturing as well as warehouse functions. Must have PHARMA EXPERIENCE Duties and Responsibilities: Under limited supervision: A...

Manufacturing Operator- Raw Materials Dispensing Summary: To perform dispensing of raw materials for manufacturing as well as warehouse functions. Must have PHARMA EXPERIENCE Duties and Responsibilities: Under limited supervision: A...

IPQA Associate I The IPQA Associate I is responsible for identifying deviations in the processes and ensure that all activities are cGMP compliant, identifying corrective actions, establishing path forward activities, and appropriate docum...

IPQA Associate I The IPQA Associate I is responsible for identifying deviations in the processes and ensure that all activities are cGMP compliant, identifying corrective actions, establishing path forward activities, and appropriate docum...