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Quality Assurance Associate I

Catalent Pharma Solutions, Inc.

This is a Full-time position in Harmans, MD posted February 23, 2021.

Job DescriptionPosition Overview:Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent’s advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start herePosition SummaryCatalent Pharma Solutions is looking to recruit a Quality Assurance Associate I-Operations to join our growing team in Harmans, MD.The Quality Associate I (QA Operations) continuously monitor systems and procedures to ensure compliance. The Quality Associate I (QA Operations) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed.The Quality Assurance Associate I (Operations) role is critical to our patients. The on the floor quality associate is responsible for making sure the process and documentation records are compliant with patient safety in mind, executing with efficiency always. Quality, safety and on-time delivery is a must to be successful in this role!The Role* Performs QA On-the-Floor activities supporting client projects, including room release, auditing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing.* Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and industry best practices.* Review and dispositions executed batch records and supporting documentation for completeness, accuracy and compliance.* Act as first responder for on the floor quality issues in a timely manner, documentation of all events/investigations and required immediate corrective actions.* Works cross-functionally with Project Management, Manufacturing, Facilities, and Quality Control in meeting project deliverables in a compliant and efficient manner* Guides personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices.The Candidate* Minimum of a B.S. in a Life Sciences discipline* +2 years’ experience within the biologic, biopharmaceutical, or regulated pharmaceutical industry* +1 years’ experience in Quality Assurance/Quality Control function* Familiarity with Good Manufacturing Practices (GMPs), 21 CFR 210/211/600s, USP and ICH GuidelinesMust possess Catalent’s standard leadership competencies that are used to interview and for Performance & Development:* Leads with Integrity and Respect* Delivers Results* Demonstrates Business Acumen* Fosters Collaboration and Teamwork* Champions Change* Engages and Inspires* Coaches and DevelopsPosition Benefits* Potential for career growth within an expanding team* Defined career path and annual performance review & feedback process* Cross functional exposure to other areas of within the organization* Medical, Dental, Vision, and 401K are all offered from day one of employment* 19 days of paid time off annually + 8 paid holidaysCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.personal initiative. dynamic pace. meaningful work.Visit www.catalent.com/careers to explore career opportunities.Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.