Planet Pharma
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Location: West Greenwich, RI; Salary: $38.00-$42.00; Posted: 4 days ago
Responsibilities
Execute routine work orders and interact routinely with end customers and vendors, ensuring reliable QC equipment support in a fast-paced environment.
Own change controls for new and/or replacing of QC equipment.
Manage the procurement of new QC equipment. Work autonomously to lead cross-functional stakeholders to identify end-user requirements, establish validation requirements and Change Control strategy.
Supports inspection readiness activities across Quality Control, and site audits and inspections.
Monitor and trouble shoot analytical benchtop equipment.
Lead projects and project planning responsibilities to ensure on time implementation of analytical instruments. Responsible to implement projects on time and on budget.
Complete all assigned tasks on time, in collaboration with key stakeholders.
Provide oversight of vendor PMs.
Create new assets and PM scheduling in Maximo.
Obtain end user requirement and vendor quotes for lifecycle replacement of equipment.
Qualifications
Min of 1+ years of experience in the biotech, pharma or medical device industry OR 1+ years of QC experience in a regulated industry
Seniority Level Associate
Employment Type Contract
Job Function Other
Industries Biotechnology Research and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Planet Pharma by 2x
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr
Location: West Greenwich, RI; Salary: $38.00-$42.00; Posted: 4 days ago
Responsibilities
Execute routine work orders and interact routinely with end customers and vendors, ensuring reliable QC equipment support in a fast-paced environment.
Own change controls for new and/or replacing of QC equipment.
Manage the procurement of new QC equipment. Work autonomously to lead cross-functional stakeholders to identify end-user requirements, establish validation requirements and Change Control strategy.
Supports inspection readiness activities across Quality Control, and site audits and inspections.
Monitor and trouble shoot analytical benchtop equipment.
Lead projects and project planning responsibilities to ensure on time implementation of analytical instruments. Responsible to implement projects on time and on budget.
Complete all assigned tasks on time, in collaboration with key stakeholders.
Provide oversight of vendor PMs.
Create new assets and PM scheduling in Maximo.
Obtain end user requirement and vendor quotes for lifecycle replacement of equipment.
Qualifications
Min of 1+ years of experience in the biotech, pharma or medical device industry OR 1+ years of QC experience in a regulated industry
Seniority Level Associate
Employment Type Contract
Job Function Other
Industries Biotechnology Research and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Planet Pharma by 2x
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr