The salary range for this role starts at $95,000-$120,000
Scope of the Role
Conduct technical assessments and provide ongoing process support for commercial Rx, OTC, and cosmetic topical products to ensure quality, efficiency, and compliance.
Lead technology transfer activities for newly developed products and transferred manufacturing processes from R&D or external manufacturing sites into commercial operations, ensuring successful scale-up and implementation.
Develop, optimize, and implement manufacturing processes for new, existing, reformulated, and transferred products to improve process robustness, efficiency, and product quality.
Investigate manufacturing issues, process deviations, and product failures; perform root cause analyses and recommend corrective and preventive actions (CAPAs).
Review, revise, and maintain Manufacturing Orders, Ingredient Disclosures, Excipient Threshold Limits, cleaning procedures, and associated documentation to support regulatory compliance and continuous improvement initiatives.
Perform laboratory-scale formulation and process development studies to support process optimization, troubleshooting, and scale-up activities.
Evaluate process performance data and identify opportunities for process improvements, cost reduction, and increased manufacturing efficiency.
Support Material Review Board (MRB) activities, including the review and disposition of nonconforming materials and products.
Participate in Process Excellence Management (PEM), Process Performance Qualification (PPQ), Continued Process Verification/Validation (CPV/CV), and other validation activities to ensure processes remain in a state of control.
Collaborate closely with Regulatory Affairs, Quality Assurance, Research & Development, Operations, and Legal teams to support product lifecycle management and maintain compliance with cGMP and FDA requirements.
Prepare technical reports, protocols, investigations, and supporting documentation required for process changes, validation activities, and regulatory submissions.
Manage multiple projects simultaneously while meeting established timelines and business objectives.
Experience Required
Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Engineering, Chemistry, or a related scientific discipline.
2–5 years of pharmaceutical manufacturing, process engineering, technical services, or process support experience in a regulated environment.
Strong understanding of pharmaceutical manufacturing processes, pharmaceutical sciences, and process engineering principles.
Knowledge of cGMP requirements, FDA regulations, and pharmaceutical quality systems.
Excellent interpersonal, organizational, and communication skills, with the ability to collaborate effectively across all levels of the organization.
Strong technical writing, documentation, and problem-solving skills.
Ability to independently manage multiple projects and priorities while meeting established timelines.
Hands-on experience with laboratory-scale manufacturing equipment and a solid understanding of commercial-scale pharmaceutical processing equipment.
Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and OneNote; experience with SAP is preferred.
Preferred Qualifications
Experience with the development, scale-up, optimization, and/or reformulation of topical pharmaceutical or cosmetic products.
Knowledge of technology transfer, process validation, and continuous improvement methodologies.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
Nearest Major Market: Bronx
Nearest Secondary Market: New York City
Apply now »
Find similar jobs
- Operations_NL,
- Operations_IT,
- Operations_ES,
- Operations_DE,
- Operations
Perrigo.com
Privacy Notice
Cookie Statement
Policies and Practices
Terms & Conditions
Opens in a new tab.
Opens in a new tab.
Opens in a new tab.
© 2022 Perrigo Company plc, All Rights Reserved.
×
Cookie Consent Manager
When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. Because we respect your right to privacy, you can choose not to allow some types of cookies. However, blocking some types of cookies may impact your experience of the site and the services we are able to offer.
Required Cookies
These cookies are required to use this website and can't be turned off.
Required Cookies
Show More Details
Required Cookies
- Provider
- Description
- Enabled
SAP as service provider
We use the following session cookies, which are all required to enable the website to function:
"route" is used for session stickiness
"careerSiteCompanyId" is used to send the request to the correct data center
"JSESSIONID" is placed on the visitor's device during the session so the server can identify the visitor
"Load balancer cookie" (actual cookie name may vary) prevents a visitor from bouncing from one instance to another
Cookies from provider SAPasserviceprovider are required and cannot be turned off
Confirm My Choices
Accept All Cookies
