Associate Specialist, Quality Product Release - Disposition

Company: Eclaro
Location: Summit
Posted on: May 28, 2023

Job Description:

Associate Specialist, Quality Product Release - DispositionJob Number: 23-01398 Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Associate Specialist, Quality Product Release - Disposition for our client in Summit, NJ.Eclaro's client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you're up to the challenge, then take a chance at this rewarding opportunity!Position Overview:Responsible for activities in accordance with corporate policies, standards, procedures, and Global cGMP in support of the QA Disposition group. Functional responsibilities include but are not limited to, ensuring accurate and timely maintenance and review of quality records and manufacturing documentation, inventory management for quality records and manufacturing documentation. Additionally, supports the receipt of executed batch records and the scanning and uploading of documents and may also support document redaction and document printing.Responsibilities:Supports the receiving of executed batch records . Supports the scanning and uploading of quality records. Contributes to the goals within the work group. Teamwork and ability to work effectively across functional groups and teams to ensure requirements are met. Work is self-directed. Confident in making decisions for non-routine issues. Proposes solutions for issues and works with management to resolve. Follows established procedures and performs work as assigned. Understands continuous improvement and improves efficiency and productivity within the group or project. Builds relationships internally within and with cross functional teams. Able to prepare written communications and communicate problems to Supervisors with clarity and accuracy. Able to effectively multi-task.Required Skills:Must be skilled in planning and organizing, decision-making, and building relationships. Must have knowledge and experience with cGMP manufacturing, Quality, and compliance. Must possess an independent mindset. Able to effectively multi-task. Knowledge of US and global cGMP requirements. Excellent verbal and written communication skills.Qualifications:B.S. degree with 1-3 years GMP experience in the Pharmaceutical or related industry or equivalent combination of education and experienceIf hired, you will enjoy the following Eclaro Benefits:401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through EclaroIf interested, you may contact:Sofia Dela Torresofia.delatorre@eclaro.com 3322060779Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.PDN-993f6384-bc8b-4399-8628-bceaeb4e704f

Keywords: Eclaro, New York , Associate Specialist, Quality Product Release - Disposition, Other , Summit, New York