Ferring
IS Applications Analyst for Manufacturing Systems
Parsippany, New Jersey, United States · Full-time
Sponsorship not specified$77k-$105kDetected 30 days ago
Project ManagementExcelERPGMPFDA RegulatoryResearchCommunicationPublic SpeakingOrganizational SkillsMicrosoft OfficeRegulatory Affairs
About the role
- With Ferring, you will be joining a recognized leader, identified as one of "The World's Most Innovative Companies" by Fast Company, and honored by Fortune with inclusion on its "Change the World List," for addressing society's unmet needs.
Responsibilities
- Provide technical and functional support for Manufacturing applications including Rockwell PharmaSuite EBR, Antares Serialization, along with associated hardware such as tablets, printers, and scanners.
- Design and configure MES eBR systems based on business requirements to digitize and automate batch record management, ensuring compliance with industry regulations (e.g., FDA's 21 CFR Part 11).
- Create, manage, and maintain electronic batch records, including recipe management, process steps, electronic signatures, and data capture.
- Maintain comprehensive documentation of system configurations, validation records, and standard operating procedures (SOPs) related to MES eBR systems.
- Develop system technical documentation, including but not limited to, functional specifications and UAT test scripts.
- Collaborate with cross-functional teams, including manufacturing, quality assurance, and regulatory affairs, to gather information and resolve discrepancies.
- Maintain data integrity by implementing periodic system reviews and audit trails for manufacturing systems.
- Maintain ThinManager or VDI for deploying software such as eBR.
- We maintain a drug-free workplace.
Requirements
- Bachelor's degree in relevant field (computer science, chemical engineering, or pharmaceutical sciences)
- Minimum 5 years of experience in Pharmaceuticals Industry.
- Proficiency in MES eBR software platforms, preferably in Rockwell Automation PharmaSuite.
- Strong understanding of regulatory requirements in industries with batch processes, including FDA regulations (e.g., 21 CFR Part 11).
- Familiarity with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) to ensure compliance.
- Proficiency in Microsoft Office Suite (Word, Excel) or equivalent software.
- Ability to move around the manufacturing plant, including walking, standing, and sitting for extended periods.
Nice to have
- Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our 'people first' philosophy.
- This role is critical in ensuring compliance with regulatory standards, optimizing batch manufacturing processes, and enhancing data integrity.
- Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country.
- Certificate/ASC/ BS in science-related discipline preferred.
Compensation
- At Ferring, base salary is one part of our competitive total compensation and benefits package and is determined using a salary range.
- The base salary range for this role is $76,831 to $105,000 which is the reasonable estimate of the base compensation for this role.
Benefits
- We are proud to offer paid parental leave subject to a minimum period of employment at Ferring.
- Additional compensation for this role will be provided based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance.
Equal opportunity
- equal opportunity employer.
- We are proud to be an Affirmative Action/
- Equal Opportunity Employer (including Disability/Protected Veterans).
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This listing is sourced directly from Ferring's careers page and normalized into a canonical job model.