Scientist, QC Microbiology

ferring
Parsippany, NJ Full Time
POSTED ON 8/9/2023 CLOSED ON 9/5/2023

What are the responsibilities and job description for the Scientist, QC Microbiology position at ferring?

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. Ferring US is Great Places to Work® Certified. Earning this certification means that Ferring US is one of the best companies to work for in the country. Our people are at the core of what makes Ferring a great place to work. Putting people first, strengthening our workplace culture, and ensuring that it is a safe, equitable, and welcoming place to work is a priority at Ferring, and it always will be. 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. The Scientist position leads and/or is actively participates in experimental design, method validation/qualification, equipment qualification and technical transfer activities of compendial methods related to raw materials and finished product. Performs routine (and non-routine) quality control testing of raw materials, in-process materials, drug substance, finished goods and stability samples. Responsible for authoring development protocols, final summary reports, investigations, change controls, risk assessments, trend reports and training. Is the subject matter expert for all microbiological methods in accordance to cGMP guidelines. Highly knowledgeable with compendial requirements and familiar with lean six sigma principles. The Scientist will collaborate with the Manager, QC and Team Leaders in support of leading and providing direction to laboratory staff for maintaining effective and efficient department operations. Leads and performs experimental design, compendia method qualifications and assay transfers to ensure successful project transfer and performance in the laboratory. Executes microbiological methods using, but not limited to, Bioburden testing, Microbial Limits Testing, Antimicrobial Effectiveness Testing, Sterility Testing, and Bacterial Endotoxin Testing, and Microbial and Fungal Identification. Executes stability program including pulling, testing, submitting to external laboratories and protocol and report generation. Performs training of new hires and assists junior analysts with water sampling, environmental sampling – routine/batch, gas testing, gown qualification and media fills. Oversee environmental performance qualification of new cleanroom areas. Performs risk assessments and develops sampling plans and site maps for new cleanroom areas. Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance; performs data trending. Supports research laboratories on experimental design and method qualification of clinical or pre-clinical products. Perform configuration of new analyses, products and specifications in LIMS as necessary. Communicates with vendors for laboratory needs. Creates, reviews, and performs authorization of GMP data on paper, logbooks and in LIMS, including but not limited to test results and records, validation protocols/reports, method transfer protocols/reports, test methods, equipment records, process transfer activities, etc. Ensures adherence to regulatory agency requirements, ICH guidelines, Ferring standards and procedures. Monitors the life cycle microbiology instruments for preventative maintenance and calibration - ensuring conformance to specifications. Ensures lab equipment conforms to specifications. Oversees the execution of IQ/OQ/PQ of new purchased instruments in a timely manner. Troubleshoots instruments in the lab when necessary. Issues deviations, laboratory investigations, corrective actions change controls, and monitors effectiveness checks in LIMS and in QA-Track. Oversees QC document management and archival and inventory control of consumables, media and garments. Assist with the budget requests, processes purchase orders and capital acquisitions requests (CAR’s). Authors SOPs, test method, specifications, developmental protocols, method qualification protocols/reports, annual product reviews and technical reports as needed. Trains junior analysts and develops training plans and/or oversee training activities for groups. Trains Micro Associates on Technical Concepts and Methods. Develops new training materials for microbiological test methods. May perform other duties as assigned by QC Micro Management. Work weekends, overtime, on-call and holidays, as needed. Requirements: Bachelor of Science Degree in Biological or Environmental Sciences from an accredited College or University is required. Master of Science degree preferred. A minimum of 8 years of QC laboratory (pharmaceutical or biopharmaceutical industry) with a Bachelor’s Degree or 4 years of industry experience with a Masters degree. Strong preference for experience in the following: Cell/Gene Therapy (CarT) TT Activities Cell-Based Assay (ELISA, PCR) Rapid Microbial Methods Working knowledge of Standard Operating Procedures (SOPs), analytical test methods, and generally accepted laboratory practices Expertise with performing laboratory investigations, change controls, and associated CAPA under limited guidance Knowledgeable in Labware LIMS configuration of new analyses and product specification. Microbiological method development, transfer, and validation experience is highly preferred. Subject matter expert for all microbiological methods in accordance to cGMP guidelines and compendial requirements and familiar with lean six sigma principles Knowledge of USP/EP/cGMP and ICH guidelines; Microbiology techniques and instrumentation; Laboratory Information Management System (LIMS); Global Quality Tracking System (TrackWise); Microsoft Office; Lean Six Sigma concepts; Lean Labs; project management; formal Quality Change Control, Investigations, and Documentation systems, and Quality Risk Management including risk assessments. Physical Requirements: Ability to stand on feet for up to four hours at a time, Be able to lift, push, and /or pull up to 25 pounds, and Meet minimal visual acuity requirements necessary for quality assessments. 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 and perform pre-employment substance abuse testing. Ferring offers a competitive total compensation package inclusive of but not limited to the following benefits: medical, dental, vision, 401(k), vacation policy, paid holidays, sick days, paid maternity/paternity leave, tuition reimbursement, flexible savings accounts, short-term disability, long-term disability, life and AD&D insurance. Location: Parsippany, New Jersey Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group committed to helping people around the world build families and live better lives. Ferring is a leader in reproductive medicine and maternal health, and in specialty areas within gastroenterology and urology. Ferring employs over 7,000 people worldwide. The company has operating subsidiaries in more than 50 countries and markets its products in over 100 countries. Learn more at www.ferring.com, or connect with us on us on Twitter, Facebook, Instagram, LinkedIn and YouTube. 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. Empowerment We create leaders and entrepreneurs We empower, we boost our teams, we incite learning. Innovation We experiment and build our future We search for new solutions, we take risks for innovation, we learn. Accountability We own everything we do with courage We seize responsibilities, we are accountable for our decisions. Collaboration We are in this together We work together across teams, functions and geographies. Transparency We listen and share We communicate honestly, we do it often, we make it simple. Purpose We share one Mission, we are guided by the Ferring Philosophy We know why we are here, we inspire each other. 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!
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