About the Company
The firm has more than 130 years of history and one of the largest health care company, this keeps its products in every stages of life. Johnson & Johnson strives to improve the quality of medicine by improving the access and affordability of medicine to the people all over the world. Foundation to vibrant lives is their main motto in the delivery of medicines. 1.3 million employees work with united heart to change the health of the humanity. Diversity is a core part of the company’s culture. Women empowerment is one of the key pillar in the company, encouraging women employee’s since 1886.
3 amazing principles in the Alzheimer’s disease. Debuts the new devise medical center at Texas. Numerous products starting from baby care products, Health care, healing products, orthopedics, surgery, interventional solutions and vision.
Pharmaceutical products including immunology, Cardio vascular, Pulmonary, Neurosciences & Metabolic diseases along with oncological drugs plays a vital role in improvising patients lives for a better society.
Recently it started in Global preventive HIV vaccine which brings an exciting milestone. The company named fortune 2019 as the most admired company, bagged top rank in linked index. Branches includes all over the world established a giant root in the pharmaceutical industry.
Right from 1887 with the introduction of Papoid tablets to band aids introduces many products in the market for mankind.
About the Job
Qualification : Bachelors in Micro or Biology or related discipline of science
Need to have 8-10 years of experience in Micro and sterile assurance role
Required to have experience in minimum 2 modes of sterilization like moist, dry/ Gamma, electronic beam with a specialization in micro practices and in a manufacturing environment is preferred.
MS or PhD is Preferred
Should have hands on experience with Operational sterilization and dealing with technical problems of process
Required to have experience in sterilization non- conformance dealing and providing robust resolutions
Should have experience in working with regulated industry and handing the query associated with cosmetics, medical devices and supplements.
Support and lead the investigations associated with the micro practices and able to provide the effective CAPA.
Required to review the generated data and handle the problems/ process from end to end
Need to train the colleagues on the regular practices of manufacturing and sterile areas support in implementation of quality assurance practices at site which are new and updated
Handling of Audits and support the external partners or audit the suppliers including the raw material, contract labs and the practices at contract labs.
Handling the micro and sterile assurance experts for the launch of new products and dealing the product life cycle management.