Product Owner (Product Lifecycle Management)

9 Minutes ago • 5 Years + • Product Management

Job Summary

Job Description

We are Haleon, a new global consumer health company focused on improving everyday health for billions. We are seeking a Product Owner for Product Lifecycle Management to own the process knowledge of assigned products throughout their commercial lifecycle. This role involves oversight of process capability, validation activities according to the Validation Master Plan to meet cGMP requirements, data trending, and statistical analysis of critical parameters, ensuring processes are robust, validated, and continuously improving at the site and CMO. The role requires acting as the principal point of contact for product knowledge, liaising with various site functions and global technical teams to ensure proper controls, and participating in product committees for improvements. The candidate will implement and maintain continued process verification, participate in trend review meetings, and maintain product control strategies and technical risk assessments. Responsibilities also include providing information for process validation, authoring validation reports, and executing cleaning validation activities.
Must have:
  • BSc. in Pharmacy/Engineering, Pharmaceutical Technology, Chemistry or equivalent scientific degree
  • Minimum of 5 years of demonstrated experience in a Technical role
  • Strong experience in TRA, Process and cleaning validation
  • Strong experience in statistical analysis of data
Good to have:
  • Desirable MSc. Engineering Or Pharm-D

Job Details

Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question.

With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we’re uniquely placed to do this and to grow a strong, successful business.

This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.

About the role

Owns the process knowledge of the product(s) assigned throughout the commercial lifecycle, maintains the oversight on process capability, through validation activities according to Validation Master Plan to meet cGMP requirements, data trending and statistical analysis of critical parameters, ensuring process(es) are robust, in continued state of validation and continuously improving at Site and CMO.

Key responsibilities

  • Recognized as the principal point of contact for all aspects of current and previous knowledge on the product(s), performance and end to end process, including critical quality attributes (CQAs) and critical process parameters (CPPs). Accountable at site level for maintaining this knowledge and sharing on site and globally as appropriate.  

  • Liaise with Regional and Global Technical, as well as other site functions such as QA, QC, Engineering, and Operations to ensure that proper controls are established and maintained for products to be manufactured in a validated state of control.

  • Actively participate in relevant product committee (e.g. Product Technical Review Team-PTRT), where the improvements on weak point products are planned, prioritized and monitored.

  • Implement and maintain continued process verification (CPV), as appropriate, for determined products and processes on site.  Incorporate data trending and statistical analysis to verify that processes remain in a validated state of control, and to proactively identify trends which may provide risk to the product.

  • Participate in Trend review meeting and providing Technical expertise to improve product Ppk.

  • Maintains and periodically reviews product control strategies (PCS) and technical risk assessments (TRA) as required. 

  • Provide all necessary information to develop and execute process validation including BHT activities, working across multiple functions to collect the appropriate inputs for validation protocols and authoring validation reports. Validates the manufacturing and packaging process parameters necessary to assure product quality, and incorporates this into the PCS.

  • Execute cleaning validation activities on the shop floor including campaign length, Dirty Equipment Hold Time (DEHT), Clean Equipment Hold Time (CEHT) and Continued cleaning process verification to ensure that all cleaning validation data, results & information are recorded accurately followed by generation of reports

Qualifications and skills

Essential

  • BSc. in Pharmacy/Engineering, Pharmaceutical Technology, Chemistry or equivalent scientific degree.

  • Minimum of 5 years of demonstrated experience in Technical role, with strong experience in TRA, Process and cleaning validation and statistical analysis of data


Preferred

  • Desirable MSc. Engineering Or Pharm-D.

Please save a copy of the job description, as this may be helpful to refer to once the advert closes.

Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/

At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.

Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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 let your recruiter know by providing them with a description of specific accommodations you are requesting. We’ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.

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About The Company

Hello. We’re Haleon. A new world-leadingconsumer healthcarecompany. Shaped by all of us. Together, we’re improving everyday health for millions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol,Advil, Voltaren,Theraflu, Otrivin,and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re building together. In anenvironment thatwe’re co-creating. And a culture that’s uniquely ours. Care to join us.

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