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Specialist Manufacturing
full-timeJuncos

Summary

Location

Juncos

Type

full-time

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About this role

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

Summary of Role: 

With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
 

Responsibilities:

Applied Process Expertise

  • Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.

  • Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.

  • Provide troubleshooting support.

  • Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.

Process Monitoring

  • Support establishment of process monitoring parameters and control limits. Collect process-monitoring data and support the assessment of deviations.

  • Provide support of timely execution of the process monitoring quarterly reports.

Non-Conformance and CAPA

  • Ensure that all Non-conformances are triaged within the established goal.

  • Responsible for authoring investigation reports.

  • Responsible for execution of corrective actions.

  • Responsible for managing NC/CAPA closure within established goal.

  • Monitor and communicate incidents trends.

  • Review equipment/system Root Cause Analysis investigations and support trend evaluations.

Process Validation

  • Assist with generation of process validation protocols and reports.

  • Assist with the execution of the process validation.

  • Support collection and analysis of process validation data.

Regulatory

  • May participate in regulatory inspections

New Product Introductions & Process or Equipment Modifications

  • Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.

  • 2. Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.

Change Control

  • Assist manufacturing change owner on CCRB packages impacting the process.

Projects and Initiatives

  • Participate on the assessment or implementation of special projects or initiatives.

Shift: Administrative 

Location: Juncos, PR 
 

Education:

Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience OR Bachelor's degree and 5 years of Manufacturing Operations experience or Associate’s degree and 10 years of Manufacturing Operations experience or High school diploma / GED and 12 years of Manufacturing Operations experience.
 

Preferred Qualifications: 

  • Bachelor's in Science or Engineering is preferred
  • Manufacturing Experience
  • Hands on experience managing CAPA & Change Controls
  • Document revisions
  • VEEVA

Skills:

  • Detailed technical understanding of bioprocessing unit operations.
  • Skilled in performance of GMP production operations.
  • Regulatory knowledge and interactions.
  • Participate and help lead cross-functional teams.
  • Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
  • Organizational, technical writing and presentation skills.
  • Basic project management skills.
  • Basic knowledge of control charting.


This position is for a fixed term contract supporting one of ECHO Consulting Group (a Cencora company) partners on site at their facility.

What Cencora offers

We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit https://www.virtualfairhub.com/cencora

Full time

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [email protected]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned

Affiliated Companies

Affiliated Companies: Echo Consulting Group Inc

Other facts

Tech stack
Manufacturing Operations,Process Validation,Troubleshooting,Regulatory Knowledge,Technical Writing,Project Management,GMP Production Operations,Cross-Functional Team Leadership,Change Control,CAPA Management,Process Improvement,Data Analysis,Document Management,Training Development,Root Cause Analysis,Process Monitoring

About Cencora

Cencora, a company building on the legacy of AmerisourceBergen, is a leading global pharmaceutical solutions organization centered on improving the lives of people and animals around the world. We connect manufacturers, providers, and patients to ensure that anyone can get the therapies they need, where and when they need them. We also help our partners bring their innovations to patients more efficiently to accelerate positive outcomes.

Becoming Cencora has allowed us to combine all the companies and services of AmerisourceBergen. Now, as a unified and internationally inclusive brand, we’re continuing to invest in and focus on our core pharmaceutical distribution business, while also growing our platform of pharma and biopharma services to support pharmaceutical innovation and access. Our 51,000 worldwide team members are shaping the future of healthcare through the power of our purpose: We are united in our responsibility to create healthier futures.

AmerisourceBergen, now Cencora, is ranked #10 on the Fortune 500 and #24 on the Global Fortune 500 with more than $290 billion in annual revenue.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Hospitals and Health Care

What you'll do

  • The Specialist Manufacturing role involves supporting the execution of manufacturing and quality systems, including process validation and non-conformance management. The position requires troubleshooting support and the generation of training materials.

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Frequently Asked Questions

What does a Specialist Manufacturing do at Cencora?

As a Specialist Manufacturing at Cencora, you will: the Specialist Manufacturing role involves supporting the execution of manufacturing and quality systems, including process validation and non-conformance management. The position requires troubleshooting support and the generation of training materials..

Why join Cencora as a Specialist Manufacturing?

Cencora is a leading Hospitals and Health Care company.

Is the Specialist Manufacturing position at Cencora remote?

The Specialist Manufacturing position at Cencora is based in Juncos, Puerto Rico. Contact the company through Clera for specific work arrangement details.

How do I apply for the Specialist Manufacturing position at Cencora?

You can apply for the Specialist Manufacturing position at Cencora directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Cencora on their website.