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Formulation PET Process Coordinator (Training Coordinator)

3.00 to 8.00 Years   Bangalore   18 May, 2022
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other SoftwareTechnical / Process Training
EmploymentTypeFull-time

Job Description

    Formulation PET Process Coordinator (Training Coordinator)Location: Mt. Vernon, INDo you have expertise in, and passion for, manufacturing in a high performing pharmaceutical environment Would you like to apply your expertise to impact the well-being of patients in a company that follows the science and turns ideas into life changing medicines We have a Process Coordinator opportunity in Formulation focused on Training. See below for specific responsibilities and qualifications.At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our peoples exceptional skills with those of people from all over the globe.The Mt. Vernon site was established in 1972 and is the flagship site delivering innovative, life changing oral solid medicines. At the site we formulate and pack OSD tablets, capsules for over 60+ markets. The Mt Vernon site is the largest AZ production site in the US and is located in the southwest corner of the state of Indiana, approximately 15 miles from Evansville, Indiana the third largest city in the state of Indiana. The Mt. Vernon site is dedicated to creating a culture of inclusion and collaboration. We host yearly Inclusion and Diversity conferences and have an employee resource group devoted to promoting diversity and inclusion and enhancing employees professional development through interactive and engaging events and initiatives.The Formulation PET Process Coordinator - Training will work closely with Process Facilitators and Operators within the Formulation PET to ensure production requirements are met or exceeded, following company policies/procedures to ensure product quality and compliance standards are met and performing all activities in a safe environment.Job Responsibilities:Advanced knowledge and understanding of equipment and manufacturing processes.Create, revise, and assist with preparation of documentation regarding training activities, actions, and/or results using GDP where applicable.Communicate policies/procedures to employees and collaborate effectively with Process Facilitator.Guide team on SOPs (Standard Operating Procedures), work instructions, and MBRs (Master Batch Records).Lead training on all document modifications prior to effective date.Review completed production documentation (for example: batch records, log books, etc.) for quality, completeness, and cGMP compliance.Author/Approve/Review/Revise/Audit SOPs, Work Instructions, and MBRs, for cGMP (Good Manufacturing Practices) manufacturing of commercial product.Coordinate cross-functionally with other departments as required.Attend team meetings to discuss progress, initiatives, and/or other matters.Read, understand, and comply with cGMP and SOPs, including general safety, lock outs, etc.Complete duty-based packets by reading SOPs and excerpts from technical documentation.Gather, organize, and communicate operational information to others.Create training modules and/or resources to ensure that SOPs are covered.Monitor key performance indicators to meet strategic goals.Monitor training of employees to ensure compliance.Required Skills and Capabilities:Experience in documentation in a cGMP environment.3 Years of experience in a pharmaceutical or cGMP regulated environment.High School diploma or equivalent.Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language.Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations.Desirable:Experience in a production environment.Bachelors degree or equivalent.Experience working in a LEAN manufacturing environment.Knowledge of cGMPs and FDA policies/procedures.Why AstraZenecaAt AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial -finding those moments and recognizing their potential. Interested Come and join our journey!Next Steps Apply today!To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.,

Keyskills :
traininglogisticsschedulingtraining programs

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