Sr Associate Quality Control Support
Sr Associate Quality Control Support
Trispoke Managed Services Pvt. Ltd.
Holly Springs, NC
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Basic Qualifications
High 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 Qualifications
Degree 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
High 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 Qualifications
Degree 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
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Seniority level
Associate -
Employment type
Full-time -
Job function
Research, Analyst, and Information Technology -
Industries
Outsourcing and Offshoring Consulting
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