IS Applications Analyst for Manufacturing Systems

Ferring Pharmaceuticals, Inc.

Parsippany, NJ

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JOB DETAILS

SALARY

$76,831–$105,000 Per Year

SKILLS

Acceptance Testing, Artificial Intelligence (AI), Automation, Biotech and Pharmaceutical, Change Control, Chemical Engineering, Code of Federal Regulations, Communication Skills, Computer Science, Computer Terminals, Computer Workstations, Corrective Action, Cross-Functional, Data Analysis, Data Collection, Data Entry, Data Quality, Desktop Virtualization, Detail Oriented, Disease, Disease Prevention and Control, Document Scanners, Documentation, ERP (Enterprise Resource Planning), Electronic Data Capture (EDC), Entrepreneurship, FDA (Food and Drug Administration), FDA Requirements, Facebook, GMP (Good Manufacturing Practices), Gastroenterology, Gene Therapy, Genetics, Healthcare, Identify Issues, Information Technology & Information Systems, Insurance Regulations, LinkedIn, MES Software, Maintain Compliance, Manufacturing, Manufacturing Analysis, Manufacturing Audit, Manufacturing Execution Systems (MES), Manufacturing Management, Manufacturing Software, Manufacturing Systems, Manufacturing/Industrial Processes, Medical Products, Medicine, Microsoft Excel, Microsoft Office, Microsoft Word, Multitasking, Oncology, Operational Support, Organizational Skills, Philosophy, Physical Demands, Printers, Process Improvement, Process Validation, Production Support, Project/Program Management, Quality Assurance, Recipe Testing, Record Keeping, Regulatory Compliance, Regulatory Requirements, Rockwell Automation, Safety Compliance, Scientific Research, Software Administration, Staff Training, Standard Operating Procedures (SOP), System Validation, Systems Administration/Management, Systems Analysis, Systems Maintenance, Team Player, Technical Support, Technical Writing, Test Scripts, Training/Teaching, Trend Analysis, Urology, Validation Documentation, Validation Plan, Validation Testing, YouTube

LOCATION

Parsippany, NJ

POSTED

4 days ago

Job Description: As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. 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. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world’s oldest enemy: disease. As the IS Applications Analyst for Manufacturing Systems, you will be responsible for the management and support of Manufacturing Systems including Rockwell PharmSuite Electronic Batch Record system (eBR) and Antares Serialization System. Responsibilities will include front-line application support, project management, validation, and end-user training. In addition, the role will need to support design, implementation, and maintenance of Electronic Batch Records (eBR). This role is critical in ensuring compliance with regulatory standards, optimizing batch manufacturing processes, and enhancing data integrity. The IS Applications Analyst for Manufacturing Systems works closely with cross-functional teams to support production operations and be comfortable analyzing data and looking at opportunities to utilize AI tools to enhance processes. 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. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country. 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. Oversee -User -Acceptance Testing of MES recipes to ensure business requirements are achieved. Plan and execute validation tests (IQ, OQ, PQ) to demonstrate compliance with regulatory requirements. Provide training to personnel on how to use eBR and Antares Serialization systems effectively. Analyze batch data and historical records to identify trends, deviations, and opportunities for process improvement. Coordinate changes to Enterprise Resource Planning (ERP) system master data, including, but not limited to, items, specifications, lookups, list of values, recipes, routings, and formulas. 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. Identify opportunities for process improvements or automation utilizing IT systems. Maintain ThinManager or VDI for deploying software such as eBR. Authoring QMS records including deviations, CAPAs (Corrective and Preventative Actions), and change controls. Co-ordinate with Product Vendor in presenting incidents and follow-up in getting solutions. Requirements: Bachelor’s degree in relevant field (computer science, chemical engineering, or pharmaceutical sciences) Minimum 5 years of experience in Pharmaceuticals Industry. Certificate/ASC/ BS in science-related discipline preferred. Proficiency in MES eBR software platforms, preferably in Rockwell Automation PharmaSuite. Knowledge of data integrity principles and strategies to prevent data corruption and maintain data accuracy and consistency. 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. Excellent communication skills to collaborate with cross-functional teams, and auditors. Ability to manage eBR projects, including planning, execution, validation, and documentation. Attention to detail and strong data-entry skills. Strong organizational skills and ability to manage multiple tasks and priorities. Proficiency in Microsoft Office Suite (Word, Excel) or equivalent software. Physical Requirements: Ability to move around the manufacturing plant, including walking, standing, and sitting for extended periods. Occasional bending, stooping, or kneeling may be required to access equipment or systems in different locations. Prolonged periods of sitting and working at a computer terminal. Repetitive motions related to keyboarding, data entry, and mouse usage. Occasionally lifting and carrying equipment or documents weighing up to 25 pounds. Ability to work in a manufacturing environment, which may include exposure to noise, dust, chemicals, or varying temperatures. Compliance with safety protocols, including the use of personal protective equipment (PPE) as required in specific plant areas. Periodic movement between different sections of the plant to liaise with production staff, review processes, or validate records. May involve climbing stairs or accessing elevated workstations. Role will be in Parsippany, NJ. Ferring + you At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. From working hours that respect your lifestyle, a culture that is welcoming and equitable, and the chance to work with the industry’s most impressive people, these are just some of the ways we live our "People First" philosophy. Our Compensation and Benefits 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. The actual amount paid may differ based on non-discriminatory factors such as experience, knowledge, skills, abilities, education and primary work location. 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. Benefits for this role include comprehensive healthcare (medical, dental, and vision) with a premium differential, inverse to base salary, to be paid by employees, a 401k plan and company match, short and long-term disability coverage, basic life insurance, wellness benefits, reimbursement for certain tuition expenses, sick time of 1 hour per 30 hours worked, vacation time for full time employees to accrue up to 120 hours in the first four (4) years of employment, and 160 hours in the fifth (5th) year of employment as well as 15 paid holidays per year. We are proud to offer paid parental leave subject to a minimum period of employment at Ferring. Ferring is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws. Join our team and your voice will be heard, and your contributions will be valued. If you love to come up with new ways to make a positive difference and see them through, you will fit right in. We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans). We maintain a drug-free workplace. Location: Parsippany, New Jersey Ferring Pharmaceuticals a privately owned, research-driven, specialty biopharmaceutical group committed to building families and helping people live better lives. We are leaders in reproductive medicine with a strong heritage in gastroenterology and urology, and are at the forefront of innovation in uro-oncology gene therapy. Ferring was founded in 1950 and employs more than 7,000 people worldwide. The company is headquartered in Saint-Prex, Switzerland, and has operating subsidiaries in more than 50 countries which market its medicines in over 100 countries. Learn more at www.ferring.com, or connect with us on LinkedIn, Instagram, YouTube, Facebook and X. At Ferring, we'll give you the tools to shape a career build on purpose. Join us and help People around the world to build families and live better lives. Click HERE to enlarge the picture. At Ferring, our focus on Patient Advocacy drives our commitment to create more equitable health outcomes for all, at every stage of their healthcare journey. We believe in everyone’s right to access the best treatment, pioneering into new therapeutic areas, and developing innovative ways to diagnose, treat and prevent diseases. Don't see the dream job you are looking for? Drop off your contact information and resume and we will reach out to you if we find the perfect fit!

About the Company

Ferring Pharmaceuticals, Inc.

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