Johnson & Johnson companies are equal opportunity employers.
ASSOCIATE BIOTECHNICIAN-00000SUI
Description
Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies is currently recruiting for an Associate Bio-Technician located in Malvern, PA.
For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of individuals with serious disease. Built upon a rich legacy of innovative firsts, Janssen Biotech, Inc. pursues innovative solutions in the therapeutic areas of immunology, oncology, urology and nephrology. With the same unwavering passion for new challenges, we dedicate ourselves to delivering solutions for these disease states where unmet needs continue to exist. Rooted in rich scientific collaborations and community-based relationships, we have access to some of the top minds in science today, allowing us to advance the treatment of patients through our innovative medicines. Our discoveries lead us not only to new treatments, but also to new ways to empower patients and expand their access to quality care. For more about Janssen Biotech, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit www.janssenbiotech.com.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion Janssen Biotech, is proud to be an equal opportunity employer.
POSITION SUMMARY:
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a cGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Responsible for fostering site pride and J&J citizenship
Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum. Support schedule adjustments to meet production, material receipt and shipping requirements; Review visual schedule. Retrieve and analyze trend charts and process data on trained procedures. Verify and enter production parameters per SOP and Batch Records. Accurately complete documentation in SOP’s, logbooks and other GMP documents. Maintain equipment and instruments. Demonstrate training progression through assigned curriculum. Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations. Wear the appropriate PPE when working in manufacturing and other hazardous working environments. Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors. Ensure materials are available for production.
Offer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity. Carry out duties in compliance with all state and federal regulations and guidelines including FDA, EPA and OSHA. Adhere to the safety code of Conduct & J&J EHS policies and attend all required EHS training. Follow Global Leadership Profile (GLP) competencies based on their leadership level within the organization (individual leader). Responsible for audit preparation and participation. Review and understand non-conformances
Qualifications
Qualifications:
This position requires a minimum of a High School Diploma or equivalent, with a minimum of 1 year of related Industry experience OR a Bachelor’s degree with no years of industry experience. Ability to work a Night Shift (7:pm- 7:30am) with a rotating weekend and holiday schedule is required. This position will utilize basic technical knowledge of Cell Growth Medium Preparation and Buffer Preparation operations which include charging of raw material components to vessels, operation of filtration skids and component addition skids as well as CIP, SIP. A working knowledge of basic cGMP requirements is preferred. Manufacturing Execution System (MES) experience is preferred.
Primary Location:North America-United States-Pennsylvania-Malvern
Organization: Janssen Biotech, Inc. (6014)
Job Function: Production
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
ASSOCIATE BIOTECHNICIAN-00000SUI
Description
Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies is currently recruiting for an Associate Bio-Technician located in Malvern, PA.
For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of individuals with serious disease. Built upon a rich legacy of innovative firsts, Janssen Biotech, Inc. pursues innovative solutions in the therapeutic areas of immunology, oncology, urology and nephrology. With the same unwavering passion for new challenges, we dedicate ourselves to delivering solutions for these disease states where unmet needs continue to exist. Rooted in rich scientific collaborations and community-based relationships, we have access to some of the top minds in science today, allowing us to advance the treatment of patients through our innovative medicines. Our discoveries lead us not only to new treatments, but also to new ways to empower patients and expand their access to quality care. For more about Janssen Biotech, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit www.janssenbiotech.com.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion Janssen Biotech, is proud to be an equal opportunity employer.
POSITION SUMMARY:
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a cGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Responsible for fostering site pride and J&J citizenship
Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum. Support schedule adjustments to meet production, material receipt and shipping requirements; Review visual schedule. Retrieve and analyze trend charts and process data on trained procedures. Verify and enter production parameters per SOP and Batch Records. Accurately complete documentation in SOP’s, logbooks and other GMP documents. Maintain equipment and instruments. Demonstrate training progression through assigned curriculum. Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations. Wear the appropriate PPE when working in manufacturing and other hazardous working environments. Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors. Ensure materials are available for production.
Offer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity. Carry out duties in compliance with all state and federal regulations and guidelines including FDA, EPA and OSHA. Adhere to the safety code of Conduct & J&J EHS policies and attend all required EHS training. Follow Global Leadership Profile (GLP) competencies based on their leadership level within the organization (individual leader). Responsible for audit preparation and participation. Review and understand non-conformances
Qualifications
Qualifications:
This position requires a minimum of a High School Diploma or equivalent, with a minimum of 1 year of related Industry experience OR a Bachelor’s degree with no years of industry experience. Ability to work a Night Shift (7:pm- 7:30am) with a rotating weekend and holiday schedule is required. This position will utilize basic technical knowledge of Cell Growth Medium Preparation and Buffer Preparation operations which include charging of raw material components to vessels, operation of filtration skids and component addition skids as well as CIP, SIP. A working knowledge of basic cGMP requirements is preferred. Manufacturing Execution System (MES) experience is preferred.
Primary Location:North America-United States-Pennsylvania-Malvern
Organization: Janssen Biotech, Inc. (6014)
Job Function: Production
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement