Product Lifecycle Specialist

Haleon; Oak Hill (FL); On-site; USD 79,000 - 130,000; Full time

Benefits offered by this job

401(k) plan

Tuition reimbursement

Paid parental leave (6 months)

Job summary

Haleon is seeking a PPR Specialist Quality Technical Writer to oversee product lifecycle documentation, annual PPR planning, and change control reviews. You will identify improvement areas, coordinate CAPA actions, and ensure compliance with GMP and global quality requirements.

You will work with cross-functional teams to simplify processes and support regulatory expectations. The role requires a Pharmacy-related degree with 5+ years of experience, strong data and writing skills, and

Qualifications

• Bachelor’s Degree in Pharmacy, PharmD or Science related.
• 5+ years of experience in a similar quality/regulatory role.
• Experience with GMP, quality systems and regulatory compliance.
• Strong written and verbal communication skills.

Responsibilities

• Follow GMP quality system procedures for PPR in line with SOPs.
• Compile PPRs in line with site procedures and timelines.
• Collect and review data; incorporate elements into PPR reports.
• Retrieve data from VQMS and SAP for investigations, CAPA and trending.
• Escalate issues to meet regulatory expectations and timelines.
• Provide assessments of PPR data and identify gaps or trends.
• Peer review PPRs written by other specialists.
• Maintain and archive PPR reports in VQDocs.
• Raise deviations and CAPA for technical gaps.
• Ensure compliance to GMP and related policies.

Skills

Quality system knowledge

Data interpretation

Verbal communication

Team collaboration

Education

Bachelor’s Degree in Pharmacy or PharmD or related Science

Tools

SAP

Veeva QMS

VQDocs

Job description

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

About the role

Oversight of the product lifecycle for the site. This includes the redaction of Periodic Product Review as per annual plans, site-wide review of change controls, oversight of stability programs and management of complaints for the site. The purpose of this role is also to identify areas of product improvement with relevant stakeholders for necessary investigation and implementation of associated CAPA in compliance with local regulatory & Quality requirement. And areas where our processes can be simplified and adapted the type of product manufactured, with an objective to make compliance easier.

Role Responsibilities

• Follow quality system and procedures for PPR in compliance with global Standard Operating Procedure requirements.
• Compile PPRs in line with the site’s procedures and established timelines.
• Collect data perform review and incorporate PPR data elements into the PPR reports as per the established PPR annual schedules/Plan.
• Retrieve data from VQMS and/or communicate with the pertinent site groups for all investigations, CAPA, and trending records pertaining to raw material, excipients, packaging components, finished product and stability acquired within the annual review period.
• Retrieve data from SAP and/or communicate with the pertinent site groups to determine the batches manufactured, packaged, or released during the annual review period, as well as the associated active and inactive ingredients utilized for the production process.
• Escalate any issues that may prevent that PPRs are completed in time and with the necessary quality to meet regulatory expectations and global internal requirements.
• Provide an overall assessment of PPR data elements and make recommendations when gaps or trends are identified; perform any data trending needed for the PPRs, where applicable.
• Perform peer review of PPRs written by other PPR Specialist Quality Technical writers.
• Identify any out of trend issues (lower Process Capability etc.) with a product with relevant functions (Technical, Stability, Production, Compliance, QA Operations, QS and QC department) to facilitate investigation and resolution of PPRs in Veeva QMS.
• Maintain and archive PPR reports and supporting documentation in VQDocs.
• Raise deviation and CAPA, if the technical gaps observed during PPR analysis.
• Comply and ensure compliance to GMP (Good Manufacturing Practices), Quality and other related policies, guidelines and requirements as applicable by law and Corporate Guidelines.

Why you?

Basic Qualifications: Bachelor’s Degree in Pharmacy, PharmD or Science related. More than eight (5) years of experience in a similar role.

Preferred Qualifications

• Has basic general technical knowledge, and specific discipline knowledge.
• Have good verbal and written skills. Can articulate issues and solutions to the team. Can produce effective project reports and presentations. Can effectively interact and collaborate with team members.
• Demonstrates respect for others. Encourages team participation.

Salary Range

The salary range for this position is from $79,000 to 130,351.11 plus an 8% Performance Bonus.

Benefits

Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering.

Job Posting End Date

2026-10-19

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong. During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon’s compliance to all federal and state US Transparency requirements.

Accommodation Requests

If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please contact us by sending an email to [e-mail]. Please include the following in your email:• Use subject line: ‘Haleon Careers: Job Accommodation Request’• Your Name and contact information• Requisition ID and Job Title you are interested in• Location of Requisition (city/state or province/country)• Description of specific accommodation you are requestingPlease note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.