ADVANCED BIO-LOGIC SOLUTIONS
Quality Assurance Senior Associate
ADVANCED BIO-LOGIC SOLUTIONS, West Greenwich, Rhode Island, us, 02817
Description:Note:This position works a rotating shift schedule, Week 1: Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday, Thursday, ~12 hours per day 6:50 AM - 7:00 PM
Ideal Candidate:
GMP experience is a must, drive, Independent but able to work within a team structure, Proficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams), Knowledge of data integrity requirements, Excellent written and verbal communication skills.
Job Details:
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities.This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.
Responsibilities Include the Following:
Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current applicable regulations.Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations.Performs review and approval of cGMP processes, procedures, documents and records. Review logbooks, batch records, attachments, work orders, and other GMP documentation.Ensure that deviations from established procedures are documented per procedures.Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.Alert management of quality, compliance, supply and safety risks.Complete required assigned training to permit execution of required tasks.Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls.Communicating and collaborating with the PQA shift to ensure required tasks are completed
Preferred Qualifications:
Bachelor's degree and 2 years of Quality/Manufacturing work experienceExperience working in a cGMP environmentExperience with decision makingExperience with analytical testing and/or general compendia testingExperience working with batch records and other GMP documentationKnowledge of data integrity requirementsProficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams)Experience collaborating within and across functional areas and demonstrated customer service focusExcellent written and verbal communication skillsAbility to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
Top 3 Must Have Skill Sets:
cGMP experienceExperience collaborating within and across functional areas and demonstrated customer service focusAbility to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
Pay Rate- between $30 - $35/Hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"
Ideal Candidate:
GMP experience is a must, drive, Independent but able to work within a team structure, Proficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams), Knowledge of data integrity requirements, Excellent written and verbal communication skills.
Job Details:
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities.This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.
Responsibilities Include the Following:
Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current applicable regulations.Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations.Performs review and approval of cGMP processes, procedures, documents and records. Review logbooks, batch records, attachments, work orders, and other GMP documentation.Ensure that deviations from established procedures are documented per procedures.Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.Alert management of quality, compliance, supply and safety risks.Complete required assigned training to permit execution of required tasks.Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls.Communicating and collaborating with the PQA shift to ensure required tasks are completed
Preferred Qualifications:
Bachelor's degree and 2 years of Quality/Manufacturing work experienceExperience working in a cGMP environmentExperience with decision makingExperience with analytical testing and/or general compendia testingExperience working with batch records and other GMP documentationKnowledge of data integrity requirementsProficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams)Experience collaborating within and across functional areas and demonstrated customer service focusExcellent written and verbal communication skillsAbility to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
Top 3 Must Have Skill Sets:
cGMP experienceExperience collaborating within and across functional areas and demonstrated customer service focusAbility to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
Pay Rate- between $30 - $35/Hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"