Specialist, Data Review

West Pharmaceutical Services, Inc; Exton (PA); Hybrid; USD 85,000 - 110,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

West Pharmaceutical Services, Inc. is seeking a Specialist, Data Review in Exton, PA, to independently review analytical data for GMP compliance and data integrity. The role requires mentoring others and applying knowledge of laboratory data review and regulatory requirements.

The position is hybrid, onsite at least 3 days per week with no relocation offered. Collaboration with Quality, Laboratory Services, and Project Management is essential to ensure accurate data interpretation and reporting.

Qualifications

• Bachelor's degree in Chemistry or a related scientific field.
• 3+ years of experience in data review, laboratory, and/or cGMP environment.

Responsibilities

• Perform cGMP Data Review on analytical data from various materials and tests.
• Review data from analytical techniques and ensure compliance to procedures.
• Review Electronic Data and Audit Trails for Data Integrity.
• Collaborate with Laboratory Services, Project Management and Quality.
• Maintain knowledge of MS Office, Master Control, LIMS, Empower and LMS.
• Manage projects from Protocol to final report.

Skills

Independent work

Multitasking

Communication

Problem-solving

Interpersonal skills

Team collaboration

Education

Bachelor's degree in Chemistry or related field

Tools

Master Control

SAP/ERP

SharePoint

Microsoft Office

Excel

Word

PowerPoint

Job description

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Title: Specialist, Data Review

Requisition ID: 75682

Date: Sep 8, 2026

Location:

Exton, PA, US, 19341

Department: Quality

Description:

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. No relocation is provided for this opportunity.

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

In this role, you will be responsible to independently provide review of analytical data for GMP compliance, accuracy, completeness, and adherence to applicable procedures and regulatory requirements. This role also requires a working knowledge of common analytical techniques and laboratory testing practices, including familiarity with laboratory data review and interpretation of analytical test results. In addition, mentor others and provide quality-minded direction as needed.

Essential Duties and Responsibilities

• Perform cGMP Data Review on the analytical data generated in WSS which may include raw materials and finished goods, product performance, container closure integrity, particle analysis, and/or microscopy/investigation.
• Review data from various analytical techniques in the laboratory including but not limited to CCI testing, USP/EP/JP/YBB Compendia Testing, ISO Testing, Instron and Zwick, ICP, DSC, TGA, IR, UV, AA.
• Review the analytical raw data generated by first and second shift laboratory operations according to established methods, protocols, compendia and work Instructions for cGMP compliance.
• Review Electronic Data and Audit Trails for Data Integrity compliance.
• Support new GMP compliance guidance and data integrity initiatives.
• Collaborate with Laboratory Services, Project Management, and Quality.
• Maintain working knowledge of computer software packages including MS Office suite, Adobe, Master Control, LIMS, Empower and LMS.
• Collaborate with analysts on proposed path forward regarding documentation questions.
• Review Internal and External Client Reports generated from lab operations from multiple analysts utilizing multiple techniques for cGMP compliance and Data Integrity.
• Review Lab Operations Methods, Protocols, and Work Instructions for cGMP Compliance.
• Manage projects from Protocol to final report.
• Review and comment on Work Instructions, Preformatted Notebooks, and Forms for Lab Operations.
• Keep current with new GMP compliance guidance and internal QA procedures.
• Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.
• Willingness to learn and review new analytical techniques.
• Meet individual and departmental goals as required.
• Conforms with and abides by all regulations, policies, work procedures, instructions, and safety rules.
• Exhibits regular, reliable, punctual, and predictable attendance.
• Other duties as assigned. #LI-AP1 #LI-ONSITE

Education

• Bachelor's degree in Chemistry or a related scientific field, preferred.

Work Experience

• 3+ years of experience in data review, laboratory, and/or cGMP environment.

Preferred Knowledge, Skills and Abilities

• Ability to work independently, multitask and thrive in fast-paced environment.
• Experience with managing Document Control activities within a regulated industry.
• Excellent written and verbal communication skills.
• Proficient in Windows OS, Microsoft Office Suite including Word, Excel, and PowerPoint.
• Familiarity with Master Control, SAP/ERP system, and SharePoint.
• Must have effective problem-solving and interpersonal skills.

Travel Requirements

None: No travel required

Additional Requirements

• Adaptable to changes in the work environment, manage competing demands and deal with frequent change, delays or unexpected events.
• Must maintain the ability to work well with others in a variety of situations.
• Effectively communicate and interface with various levels internally and with customers.

What We Offer

Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities. Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives. Generous Paid Time Off (PTO):Flexible vacation, personal, and holiday leave ensures employees can maintain a healthy work-life balance and recharge effectively. Global Career Opportunities: With facilities across North America, Europe, and Asia-Pacific, employees have opportunities for international exposure and cross-functional collaboration. Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment. Recognition & Rewards:Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.

Shift

Monday - Friday

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in orderto apply to West, please send an email to [e-mail] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.