15 Sr Associate Quality Control Support Jobs in Holly Springs, NC
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Sr Associate Quality Control Support
$75k-102k (estimate)
Full Time
3 Weeks Ago
Trispoke Managed Services Pvt. Ltd. is Hiring a Sr Associate Quality Control Support Near Holly Springs, NC
Basic QualificationsHigh School/GED 4 years of Quality work experience OR
Associate’s degree 2 years of Quality work experience OR
Bachelor’s degree 6 months of Quality work experience OR
Master's degree
Preferred QualificationsDegree in a related scientific field such as Chemistry, Microbiology, Molecular Biology, Physics or Engineering or Information Systems.
3 years of relevant experience in the GMP commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry.
Previous laboratory experience.
Strong knowledge of validation of LIMS & LMES/CIMS.
Experience in a lead role, providing guidance to team members.
Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery.
Strong written and verbal communication skills including technical writing and presentation.
Familiar with authoring or owning change control records.
Experience with equipment and method validation, verification, and transfer including the change control process.
Interact effectively with variety of communication and working styles and ability to work well in teams.
Thrive!
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
#Chemistry #Bio #pharmaceutical #Lab #Biotech #Biopharma #chemical #LMES #CIMS #Microbiology #Molecular #GMP #laboratory #regulatory #compliance #QA #QC #Qualitycontrol #Qualityassurance #validation #For more jobs visit https://www.linkedin.com/company/trispoke-managed-services-pvt-ltd/jobs/?viewAsMember=true 12753
Associate’s degree 2 years of Quality work experience OR
Bachelor’s degree 6 months of Quality work experience OR
Master's degree
Preferred QualificationsDegree in a related scientific field such as Chemistry, Microbiology, Molecular Biology, Physics or Engineering or Information Systems.
3 years of relevant experience in the GMP commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry.
Previous laboratory experience.
Strong knowledge of validation of LIMS & LMES/CIMS.
Experience in a lead role, providing guidance to team members.
Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery.
Strong written and verbal communication skills including technical writing and presentation.
Familiar with authoring or owning change control records.
Experience with equipment and method validation, verification, and transfer including the change control process.
Interact effectively with variety of communication and working styles and ability to work well in teams.
Thrive!
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
#Chemistry #Bio #pharmaceutical #Lab #Biotech #Biopharma #chemical #LMES #CIMS #Microbiology #Molecular #GMP #laboratory #regulatory #compliance #QA #QC #Qualitycontrol #Qualityassurance #validation #For more jobs visit https://www.linkedin.com/company/trispoke-managed-services-pvt-ltd/jobs/?viewAsMember=true 12753
Job Summary
JOB TYPE
Full Time
SALARY
$75k-102k (estimate)
POST DATE
05/30/2024
EXPIRATION DATE
10/09/2024
Show more
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