Quality Control Associate

4 days ago

West Greenwich, United States SSi People Full time

Description:


The hiring manager is interested in reviewing candidates who are recent graduates, preference of candidates with a science background education wise, would like to see previous lab experience on resume.

Reporting hours for the EW's: This is a 100% onsite role and the EW's will need to report every day to the Amgen Rhode Island (USRI) location. Shift hours will be a standard 8 hour day. Need to have EW's start by 8:30 AM ET and can start/arrive an hour earlier if they wish and complete an 8 hour day following that.

What will the EW's work environment look like? Lab based work environment, although the EW's will not be doing any testing.

Interviews will be onsite interviews: 4 interviews total at 30 minutes each for 2 hours total onsite in Rhode Island.


Full time onsite - 8-5 (Flexible)


Open to a recent graduate or someone with 0-2 years of related experience.

Must Have: Baseline industry knowledge in Pharma. Possibly a candidate who took relevant coursework in college.

Nice to have: Testing or lab experience around analytical instruments in quality control testing.


QC Senior Associate:

The Amgen Rhode Island Quality Control Equipment group is responsible for the end to end life cycle of equipment in QC. This includes procurement, development, and execution of validation and change control strategy, oversight and execution of general and preventative maintenance activities, and decommissioning support as required.


This position is a full time on-site position at ARI (West Greenwich, RI location)


Responsibilities will include, but are not limited to:

• 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.


What we are looking for:

• Experience in writing and managing Change Controls

• Experience in executing general, preventative, and corrective maintenance in Maximo system.

• Validation experience (Lab equipment, computer related systems)

• Focus on data integrity and cGMP practices

• Project management

• Proficiency in Excel, Word, and PowerPoint, Outlook, and Project

• Strong interpersonal skills

• Excellent written and verbal communication skills (including technical writing and presentations)

• Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.

• Demonstrated ability to work independently and deliver right first-time results

• Commitment of 40 hour work week in West Greenwich, RI. This is a full time on-site role


Experience:

• Bachelor’s degree and 2 years of Quality/ Operations Experience

OR

• Associate's degree and 3+ years of Quality/ Operations Experience

o OR

• High school diploma/GED and 4+ years of Quality/ Operations Experience


Preferred Qualifications

• GMP and GDP experience in a laboratory setting.

• Proficient in Trackwise, Maximo, CDOCS

• Experienced in Quality systems, including Change Control, Deviations, CAPA

• Experienced in Quality processes, including validation and data integrity

• Proficient in problem solving and LEAN principles

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