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Candidate for this role can sit in Metro NY, Long Island or Connecticut
AutoZone\'s Part-Time Retail Sales Associates drive sales through superior customer service by exceeding customer expectations and providing a WOW! Customer Service experience. While assisting customers, the Retail Sales Associate will perform daily assigned duties and remain compliant with company procedures in accordance to AutoZone expectations by Living the Pledge every day.
Overview
Allied Universal®, North America’s leading security and facility services company, provides rewarding careers that give you a sense of purpose. While working in a dynamic, diverse and inclusive workplace, you will be part of a team that fuels a culture that will reflect in our communities and customers we serve. We offer medical, dental and vision coverage, life insurance, retirement plan, employee assistance programs, company discounts, perks and more for most full-time positions!
Description We are seeking an Indemnity Claims Specialist to join our team. This role is based in CENTRAL ISLIP, New York, 11722-4530, United States. The chosen candidate will manage WC Indemnity claims within established standards and practices, ensuring the best possible outcome. This role offers a short term contract employment opportunity and can be performed remotely.
Job Posting
Facilities Maintenance Technician Urgently Hiring
About CiplaCipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India\'s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.Driven by the purpose \'Caring for Life\', Cipla\'s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.InvaGen Pharmaceuticals, Inc.InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla\'s respiratory business in the United States.Job TitleQA DirectorOrganization NameInvaGen PharmaceuticalsLocation550 South Research Place Central Islip, NY 11722 7 Oser Ave, Hauppauge, NY 11788Employment Type (Hourly/ Full Time)Full Time - Salaried/Exempt Salary Range(Base/ Hourly)$165,000 - $190,000BenefitsIn addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefitsWork Hours/ Shift/ Remote8:30 AM - 5:00 PMResponsibilities/ AccountabilitiesThe general duties and responsibilities of the \"Director QA \" include but are not limited to the following: Develop, establish and maintain Quality Management System as per 21 CFR Part 11 requirements for products manufactured at Invagen New York facility. Accountable to ensure product quality of all manufactured and released products at site. Ensure compliance of products manufactured at site. Ensure the highest standard of Data integrity is maintained at site. Ensure compliance of all quality unit personnel in maintaining a safe work environment. Ensure compliance with cGMP as laid down in the procedures. Review and or approval of Deviation, change control, CAPA, complaints and Laboratory non-conformance. Accountable for Batch disposition based on its testing results. Development of talent in the Quality organization. Subject matter expert on technical and compliance issues related solid oral drug products and Drug Device combination products. Ensure and maintain the facility as per all-time audit readiness mode. Conduct management review meetings to apprise Senior management on the effectiveness of QMS for combination products and other Drug products manufactured in the facilities. Ensure compliance with all good documentation practices. Ensure adequate investigation and timely closure of QMS action items. Ensure implementation and effectiveness check of global CAPA at site. Ensure Qualification and validation of Equipment\'s, Facilities and Process for the sites, Support for submission of internal and external audit response on timely manner.Education Qualifications Minimum a bachelor\'s degree in science/pharmacy or equivalent area of Science. Master\'s degree in a science related field is preferred. ExperienceExperience in Operation Quality of Pharmaceutical drug products must include Drug Device combination products.Around 10 to 15 years of experience in areas of Operational quality including at least 5-7 years in a leadership role in a Regulated Pharmaceutical Industry environment. Should have all required regulatory compliance knowledge and competency for drug product manufacturing, environmental monitoring, area classification requirements.Skills/ CompetenciesPossess excellent Technical Writing capabilities.Proficiently communicate and understand (speak, read and write) scientific work in English.Have excellent communication and coaching skills.Ability to understand and analyze complex data sets.Strong desire towards continuous improvements.Proficient with Microsoft Office programs and other software based QMS platforms like Master control, TracwisePhysical RequirementsAble to wear appropriate personal protective equipment at all times, when required. Sitting at a desk and/or working at a computer or other \"screen\" 75% or greater of an 8-hour period.Other InformationNo remote work available. Relocation available. Equal Opportunity EmployerCipla USA & its U.S. Affiliates are committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard towithout regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected bylocal, state, or federal laws, rules, or regulations.At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact careers.northamerica@cipla.com.Pre-employment ProcessApplicants who receive a conditional offer must satisfactory complete pre-employment drug testing.Disclaimer on Pay RangesAbout the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.
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