Quality Manager

Posted 8 Hours Ago
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Freeport, TX, USA
In-Office
Expert/Leader
Information Technology • Utilities • Big Data Analytics
The Role
Lead site quality and compliance to GMP and ISO standards; manage QA lab operations, testing, audits, supplier quality, customer complaints, CAPAs, MOC, and continuous improvement to ensure product quality and regulatory compliance.
Summary Generated by Built In

The Role:

The Quality Manager will ensure that the site meets GMP, compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality.

How You Will Make an Impact:

  • Ensure EHS compliance and continuous improvement in EHS performance
  • Ensure department goals and KPIs are aligned with site objectives
  • Develop budget plans following a zero-based approach and manage Quality costs
  • Provide site strategy for quality management
  • Be the Management Representative for obtaining and maintaining quality certifications (ISO 9001 etc.)
  • Oversee execution of raw material and finished good testing and COA generation
  • Provide site strategy and procedures for maintenance of analytical data and document control
  • Provide strategy for in-process quality control
  • Oversee laboratory, analytical equipment and facilities
  • Review customer specifications and ensure that processes are capable
  • Analyze and lead improvement efforts related to process capabilities (CpK) of production processes to eliminate product defects
  • Focal point for site customer complaint investigation and response processes
  • Ensure EHS compliance and continuous improvement in EHS performance
  • Assure a compliant quality operation (incl. e.g. Responsible Care, ISO 9001/14001)
  • Manage QA aspects of the site MOC process for pharma and non-pharma operations.
  • Create and improve customer engagement touchpoints for matters related to product quality and regulatory compliance
  • Assess and evaluate supplier quality processes to ensure alignment with SI quality standards; apply corrective action accordingly
  • Oversee audit and investigation processes related to quality and for corrective measures to achieve and maintain compliance
  • Evaluate and improve quality process work plans to reduce product rejection rates
  • Assure the operation, maintaining, and improvements of the site's GMP and MOC processes
  • Maintain FDA export certifications for regulatory bodies world-wide (US, Canada, EU, Mexico, Brazil, Japan) when applicable
  • Active participation in any regional QA associated initiatives (internal/external)
  • Serve as member of Site Leadership Team
  • Work with other functional leaders to identify and solve problems to support achievement of site goals
  • Anticipate future requirements for site and develop strategic plans to meet them

Creating Extraordinary Starts With:

  • Bachelor's degree in Chemistry or Chemical Engineering, or other STEM discipline
  • Minimum of ten years' experience in process industry manufacturing
  • Minimum of five years Supervisory experience
  • Deep level of chemistry knowledge with training in analytical chemistry and experience in raw material and finished good testing, in-process quality control, Quality Certification Management, quality auditing quality statistics
  • ISO 9001, 1400, RC1400 knowledge certification; ISO Auditor; cGMP certifications preferred

What We Value:

We strive for all employees to nurture physical, mental and emotional health both personally and professionally. Our commitment to health and wellness centers around prevention, early detection and embracing a healthy lifestyle. Some offerings may vary by role or region, but may include: 

  • Physical Health benefits including competitive Medical, Dental, and Vision packages, company contribution to Health Savings Account, cash incentive for Annual Physical and reimbursement
  • Financial Wellness opportunities including company paid life insurance and disability plans, 401(k) Retirement Plan with generous company match, and certified Financial Planning & Investment services
  • Mental Health benefits including generous Paid Time Off and 10 Paid Holidays, Paid Parental Bonding Leave, and much more!   
About UsEssential Solutions with Extraordinary Results

SI Group is a global leader in the innovative technology of performance additives, process solutions, active pharmaceutical ingredients, and chemical intermediates. Our solutions are essential to many diverse industries and applications, creating extraordinary results. We drive value by enhancing the quality, performance, and durability of countless items we use every day. 

We are on a journey to captivate our customers at every level. Whether that means expanding our capabilities, global reach, or providing new innovations and technologies that create value. Our approach is customized to exceed customer needs and deliver superior performance.

Skills Required

  • Bachelor's degree in Chemistry, Chemical Engineering, or other STEM discipline
  • Minimum of ten years' experience in process industry manufacturing
  • Minimum of five years supervisory experience
  • Training in analytical chemistry and experience in raw material and finished good testing
  • Experience in in-process quality control and maintaining GMP processes
  • Experience in quality certification management, quality auditing, and quality statistics (process capability CpK)
  • Knowledge/certification in ISO 9001, ISO 14001, Responsible Care; ISO Auditor and cGMP certifications

Oracle Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Oracle and has not been reviewed or approved by Oracle.

  • Healthcare Strength Health coverage is described as broad and highly subsidized, with multiple plan choices, immediate eligibility, and added services like telehealth and mental health support. Benefits include company HSA contributions and fully subsidized options for some dental and vision plans.
  • Leave & Time Off Breadth Time off options span accrued vacation, flexible vacation for salaried roles, a winter break, and a wide range of leaves including parental, caregiver, bereavement, military, and jury duty. Feedback suggests paid sick time and volunteer hours further support balance beyond core vacation.
  • Parental & Family Support Family supports include paid parental leave, caregiver leave, elder‑care resources, and assistance for fertility, surrogacy, and adoption. These programs indicate structured support for major life events alongside core medical benefits.

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The Company
HQ: Austin, TX
211,840 Employees
Year Founded: 1977

What We Do

We’re a cloud technology company that provides organizations around the world with computing infrastructure and software to help them innovate, unlock efficiencies and become more effective. We also created the world’s first – and only – autonomous database to help organize and secure our customers’ data. Oracle Cloud Infrastructure offers higher performance, security, and cost savings. It is designed so businesses can move workloads easily from on-premises systems to the cloud, and between cloud and on-premises and other clouds. Oracle Cloud applications provide business leaders with modern applications that help them innovate, attain sustainable growth, and become more resilient. The work we do is not only transforming the world of business--it's helping defend governments, and advance scientific and medical research. From nonprofits to companies of all sizes, millions of people use our tools to streamline supply chains, make HR more human, quickly pivot to a new financial plan, and connect data and people around the world.

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