Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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MCS Associate Quality Control
Posted: 09/27/2024
2024-09-27
2024-11-12
Employment Type:
Contract
Job Category: Quality and Compliance
Job Number: 614772
Is job remote?: No
Country: United States
Job Description
Target PR Range: 19-25/hr
*Depending on experience
Job Details: Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Preferred Qualifications
? Ability to adhere to regulatory requirements, written procedures and safety guidelines
? Ability to evaluate documentation/data according to company and regulatory guidelines
? Ability to organize work, handle multiple priorities and meet deadlines
? Strong written and oral communication skills
? Must be detail orientated
? Must be flexible and adaptable to changing priorities and requirements
? Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
? Demonstrates understanding of when and how to appropriately escalate.
? May identify, recommend and implement improvements related to routine job functions.
? Must learn and comply with safety guideline and cGMPs.
*Depending on experience
Job Details: Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Preferred Qualifications
? Ability to adhere to regulatory requirements, written procedures and safety guidelines
? Ability to evaluate documentation/data according to company and regulatory guidelines
? Ability to organize work, handle multiple priorities and meet deadlines
? Strong written and oral communication skills
? Must be detail orientated
? Must be flexible and adaptable to changing priorities and requirements
? Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
? Demonstrates understanding of when and how to appropriately escalate.
? May identify, recommend and implement improvements related to routine job functions.
? Must learn and comply with safety guideline and cGMPs.
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Ready to take your career to the next level in the vibrant city of Thousand Oaks, California? Nestled in the heart of Ventura County, this bustling city offers a perfect blend of suburban charm and urban amenities. With a strong job market, top-notch schools, and breathtaking views of the Santa Monica Mountains, Thousand Oaks is an ideal location for professionals seeking growth and fulfillment. Explore job opportunities near iconic sites like the Gardens of the World, catch a show at the Fred Kavli Theatre, or indulge in the local culinary scene featuring dishes from around the world. Join this dynamic community and unlock your potential in Thousand Oaks! Start your job search now to find your perfect fit in this captivating city.
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