Manufacturing Ops Associate Job at Hewlett Packard Enterprise (Aguadilla)

Quality Systems College Co-op

We are searching for a Quality Systems Co-op to contribute to our Global Quality...

Location

United States , Three Rivers

Salary:

Not provided

American Axle & Manufacturing

Expiration Date

Until further notice

Requirements

Currently pursuing a Bachelor's degree fulltime in Engineering or related field with a graduation date of May 2027 or later
Available to work 25 hours per week year-round
Minimum 3.0 GPA
Must be able to work in the US without Visa Sponsorship

Job Responsibility

Learn about AAM Q4 Quality System
Create and follow standardize work
Utilization of Quality Systems – SharePoint, APEX, IQS, IPF
Interfaces with plant Quality, Engineering and Production Teams
Issue CARS (corrective action reporting) and track to completion
Assist with Supplier Quality engineering activities associated with manufacturing FTQ and OEE loss
Assist with troubleshooting daily production defects through root cause analysis techniques as they occur
Issue PRR’s to suppliers for defects regarding line downtime
Capture downtime, driver, and sort cost to supplier issues
Implements safety and good housekeeping standards

Parttime

QA Specialist

You will be a member of Pfizer’s dedicated and highly effective quality assuranc...

Location

Ireland , Dublin; Newbridge; Shanbally; Ringaskiddy; Little Island

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Relevant Third Level Qualification or Equivalent (Exceptions may be considered where relevant skills/experience and correct attitude and behaviours exist (this may be supplemented by further education in parallel)
Minimum 2 years experience as detailed above in the job responsibilities section, within a QA/QC GMP environment in a Pharma/Biotech company
Excellent communication and interpersonal skills
An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment
Proactive approach and strong critical thinking skills

Job Responsibility

Support operations through real time batch review ensuring all batch manufacturing records (paper / electronic) and associated manufacturing deviations are reviewed in a timely manner and in accordance with release schedules
Support issue resolution, incident routing and deviations
Complete walkthrough audits to ensure the area is maintaining cGMP compliance standards
Attend IMEx meetings and ensure timely escalation of issues to the QA Manager
Accurately communicate Supply/Operational needs/perspectives as well as Quality Operations (QO) perspectives
Review and approval of validation documents Process, cleaning & method validation
Review and approve master batch records and executed batch records to assure compliance with regulatory standards and regulatory filings
Ensure that production instructional documentation (SOPs and batch records) are up to date, compliant, and supports RFT (right first time) production, and that all in -process control limits and specifications have been met
Review all operational SOP’s, forms, protocols and reports, and any related documentation as applicable
Ensure all batch deviations are reported in accordance with Pfizer corporate standards

Fulltime

Specialist QA - Drug Substance Ops

In this vital role you will oversight on-the-floor operations, you will be respo...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
or Master’s degree and 2 years of Quality or Manufacturing support experience in pharmaceutical, GMP regulated environment
or Bachelor’s degree and 4 years of Quality or Manufacturing support experience in pharmaceutical, GMP regulated environment
or Associate's degree and 8 years of Quality or Manufacturing support experience in pharmaceutical, GMP regulated environment
or High school diploma / GED and 10 years of Quality or Manufacturing support experience in pharmaceutical, GMP regulated environment

Job Responsibility

Execute Quality disposition (approval or rejection) of bulk drug substances
Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations
Ensure that deviations from established procedures are identified, reported, and documented per procedures
Ensure that changes that could potentially impact drug substance quality are assessed according to procedures
Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements
Ensure that facilities, equipment, materials, organization, processes, and procedures align with cGMP practices and other applicable regulations
Champion continuous improvement initiatives, programs, and projects, including developing efficiency projects and supervising progress
Ensure completion of required training and maintain assigned training adherence to support successful task execution
Collaborate and partner cross‑functionally to ensure the Quality Management System (QMS) processes are completed in accordance with established procedures
Support internal and external audits and inspections as part of the audit/inspection management team, including acting as Quality Unit representative as needed

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown

Fulltime

New

Supv II, Facilities & Maintenance

The primary responsibility of the Maintenance Supervisor is to ensure the safe, ...

Location

United States , Hayward

Salary:

80000.00 - 110000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Associate degree or equivalent experience required
Bachelor's preferred
Minimum 2 years in a manufacturing environment
Familiarity with Lean Manufacturing and Six Sigma
Strong understanding of mechanical, electrical, and pneumatic systems
Proficient in reading blueprints, manuals, and SOPs
Knowledge of hazardous materials, OSHA, EPA, and FDA regulations
Excellent communication and documentation skills
Ability to simplify procedures and improve efficiency
Attributes: integrity, work ethic, judgment, innovation, accountability, and respect

Job Responsibility

Maintain a safe work environment in compliance with safety policies
Supervise maintenance and facilities activities across two shifts (up to 16 hours/day, 5 days/week)
Develop and manage predictive and preventive maintenance programs per FDA 21 CFR Part 820
Document procedures, PM work orders, reports, and validation protocols
Support CAPA investigations using root cause analysis tools
Oversee contract services (cleaning, security, pest control, outsourced PM)
Schedule and coordinate CM and PM work via CMMS
Monitor equipment OEE and reliability data
troubleshoot failures
Analyze downtime and spare part usage to optimize reliability

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Supv II, Facilities & Maintenance

The primary responsibility of the Maintenance Supervisor is to ensure the safe, ...

Location

United States , Hayward

Salary:

80000.00 - 110000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Associate degree or equivalent experience required
Bachelor's preferred
Minimum 2 years in a manufacturing environment
Familiarity with Lean Manufacturing and Six Sigma
Strong understanding of mechanical, electrical, and pneumatic systems
Proficient in reading blueprints, manuals, and SOPs
Knowledge of hazardous materials, OSHA, EPA, and FDA regulations
Excellent communication and documentation skills
Ability to simplify procedures and improve efficiency
Attributes: integrity, work ethic, judgment, innovation, accountability, and respect

Job Responsibility

Maintain a safe work environment in compliance with safety policies
Supervise maintenance and facilities activities across two shifts (up to 16 hours/day, 5 days/week)
Develop and manage predictive and preventive maintenance programs per FDA 21 CFR Part 820
Document procedures, PM work orders, reports, and validation protocols
Support CAPA investigations using root cause analysis tools
Oversee contract services (cleaning, security, pest control, outsourced PM)
Schedule and coordinate CM and PM work via CMMS
Monitor equipment OEE and reliability data
troubleshoot failures
Analyze downtime and spare part usage to optimize reliability

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Supply Planning Specialist

Reality Labs (RL) at Meta is a pioneer in the development and manufacturing of i...

Location

United States , Sunnyvale

Salary:

114000.00 - 168000.00 USD / Year

Material Planning Manager

The Material Planning Manager is responsible for leading material planning activ...

Location

United States , Tampa

Salary:

Not provided

AEVEX Aerospace

Expiration Date

Until further notice

Requirements

Strong working knowledge of MRP/ERP systems (e.g., SAP, Oracle, NetSuite, Microsoft Dynamics)
Experience in a manufacturing or regulated production environment
Strong analytical, problem-solving, and decision-making skills
Strong background in continuous improvement methodologies (Lean, Six Sigma)
Bachelor’s degree in Supply Chain Management, Business, Operations, Engineering, or related field
10+ years of experience in material planning, supply chain, or manufacturing operations
5+ years of people management or team leadership experience
Experience with S&OP / IBP processes
Experience managing materials in a complex, multi-product or program-based environment
Ability to obtain/maintain a Secret DoD clearance, U.S. Citizenship required

Job Responsibility

Develop and execute material plans to support production schedules, customer demand, and business objectives
Ensure timely availability of raw materials, components, and subassemblies to support manufacturing and program requirements
Monitor and optimize inventory levels to balance service levels, cash flow, and storage constraints
Establish and maintain safety stock policies and planning parameters
Translate production schedules and forecasts into accurate material requirements using MRP/ERP systems
Identify and mitigate material constraints, shortages, and risks to production continuity
Partner with Procurement and Material Program Managers to manage lead times, capacity constraints, and material availability
Work cross-functionally with Manufacturing, Quality, Engineering, and Finance to resolve material issues and support program execution
Drive continuous improvement initiatives to enhance material planning accuracy, efficiency, and visibility
Support ERP/MRP system enhancements, data accuracy initiatives, and planning tool implementations

What we offer

401(k)-retirement plan
comprehensive Medical, Dental, Vision, Disability and Life insurance group coverage with a portion of the premiums paid by the company
professional development funds
an Employee Assistance Plan (EAP) with counseling, legal help, child and elder care support

Fulltime

Associate Director, CMC Operations

Manage the flawless execution of Kailera’s CMC activities, spanning departmental...

Location

United States , Waltham

Salary:

160000.00 - 200000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

10+ years of experience in pharmaceutical drug development, clinical and/or commercial manufacturing familiarity, and track record of success supporting multiple projects or programs simultaneously
Excellent communication/presentation skills and proficiency in Smartsheet software
Proven track record of creativity, problem solving, and productivity, particularly when no or minimal precedent is in place
Demonstrated successful experience with working in interdisciplinary and cross-cultural teams
Bachelor’s degree in a scientific discipline preferred

Job Responsibility

Support execution of CMC-related projects, culminating in the successful preparation of regulatory submissions and product approvals
Actively support Tech Ops strategies and goals by participating in and/or leading cross-functional CMC sub-teams
Work closely and collaboratively with Tech Ops, Quality, Regulatory, and Finance colleagues to maintain highly efficient practices for pharmaceutical product development and budget management activities
Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team members
Ensure quality, quantity, and timelines in all assigned projects
Update team members on project target dates and priorities. Proactively contributes to budget forecasts and tracking expenses

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Manufacturing Ops Associate

Hewlett Packard Enterprise

Location:
Puerto Rico , Aguadilla

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
September 04, 2025

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