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Title:  Quality Control Lead

Requisition ID:  70101
Date:  Jun 9, 2025
Location: 

Jersey Shore, Pennsylvania, US

Department:  Quality
Description: 

 

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  

 

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.  

 

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.  

Job Summary

 

Schedule-12 hr-night shift ( D shift)

The QC (Shift Leader) will help lead and develop the QC team. This is a working lead position performing all duties of the Quality Inspector.  The QC lead is an acting point of contact for the plant when QA supervisors/management is not present. The QC lead will communicate product and work-related issues to the site so necessary actions may be taken.

Essential Duties and Responsibilities

  • Lead the QC team and coordinate their daily activities to ensure optimum resource planning and a fully motivated, competent workforce. Take corrective action when necessary.
  • Carry out QC tasks as required, ensuring all QC functions are performed accurately and effectively.
  • Monitor and enforce compliance to a high level of work standards across the QC functions. Ensure that jobs are carried out efficiently. Paperwork is maintained accurately in accordance with Company policies, Regulatory standards and Training.
  • Ability to inspire action by working closely with their team. Lead with confidence, may face difficult challenges, but solves them and help maintain Team morale.
  • Ensure that technical equipment is regularly checked, appropriate paperwork is maintained and corrective action taken when necessary.
  • Monitor the care of all department equipment and company property.
  • Provide as a central point of communication for all departments in respect to product quality issues ensuring that all direct communication is cascaded to the Production Area Manager, Leads and the QC team.
  • Actively engage in problem solving, solution finding and escalate process abnormalities.
  • Ensure West’s processes are operating at the highest Quality.  Support process improvement activities.
  • Guide and coach inspectors on their team. Support QC team personnel while working in a team-oriented environment.
  • Advise production staff on product information, usage and rejections as required.
  • Provide second opinions and check standards for consistency against specifications.
  • Maintain consistent standards of operation in readiness for customer visits to the site at all times.
  • Ensure that QC areas are kept clean at all times and cleaning schedules are followed.
  • Exhibits reliable and punctual attendance.
  • Conforms with and abides with work procedures, instruction, and all safety rules.
  • Maintain a high level of confidentiality when applicable.

Education

  • High school diploma or required

Work Experience

  • Prefer at least 3 years of related experience analyzing information, documentation skills, promoting process improvement and safety,management #L

Preferred Knowledge, Skills and Abilities

  • Familiarity with a variety of Quality concepts, practices, AQL sampling plans for attribute and dimensional inspection.
  • Experience with DR/NC initiation, bracketing requirements, investigation process and corrections to take.
  • Understanding processes from Extrusion to Final Pack and Westar, manufacturing methods and procedures; support innovation, Quality Engineering and Operations research.
  • Familiarity with Stopper knowledge, West drawings, configurations, formulations, coatings and use of the product.
  • Support Intermixes and work with the Intermix Site Champions.
  • Relies on extensive experience and judgment to plan and accomplish goals.
  • Performs a variety of tasks, able to communicate and pay attention to detail.
  • Wide degree of creativity and latitude is expected.
  • Functional understanding of cGMPs
  • Basic computer skills (Excel and SAP experience preferred)
  • Willing and able to work as a team to make general decisions within authorized responsibility
  • Willing and able to work overtime within the department as necessary or advised
  • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute in Lean Sigma programs and activities towards delivery of the set target
  • Able to comply with the company’s safety policy at all times
  • Able to comply with the company’s quality policy at all times.

Travel Requirements

None: No travel required

Physical Requirements

Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.

 

 

 

West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.  

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