QA Process Microbiologist

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function

Quality

Job Sub Function

Quality Assurance

Job Category

Professional

All Job Posting Locations:

Malvern, Pennsylvania, United States of America

Job Description

Johnson & Johnson is recruiting for a Quality Control Supervisor, located in Raritan, NJ!

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are currently seeking a highly qualified individual to join our Quality team as a Lead Process Microbiologist at our Clinical and Commercial Large Molecule Drug Substance Manufacturing facility. In this key role, you will be responsible for leading the Process Microbiology team in the development and/or improvement and maintenance of the contamination prevention programs and microbiological hygiene programs. Acting as a microbiological SME and working with investigators on microbiological contamination issues in the facility and providing pragmatic advice to production operators, team leaders and management on topics concerning contamination risk prevention. If you are passionate about quality/microbiological positions in the pharmaceutical industry and possess the necessary skills and experience, we invite you to apply for this exciting opportunity as a Lead Process Microbiologist. Join our team and contribute to the development of life-saving therapies in a dynamic and rewarding environment!

Key Responsibilities

• Supports improvements and preventative actions related to the reduction of contamination risks and the improvement of microbiological hygiene as a result of risk analysis, and ensures that these improvements are realized and implemented.
• Provides meaningful input on the aseptic techniques involved in process steps and other areas related to contamination control such as equipment/facility design, cleaning & disinfection, gowning and transport of man & materials into and throughout the facility.
• Participates in and supports technical investigations of products or processes
• Analyzes environmental monitoring, water system and utility data for trends.
• Reviews and/or approves technical documents, reports and procedures.
• Maintains a presence on the shop floor where he/she will work closely together with the operators and management of the Manufacturing, and Maintenance departments.
• Works closely with other key stakeholders including the QC Microbiology SME, QC personnel, Quality Assurance, Quality Systems, Compliance groups and Operations.
• Represents the QA department in meetings or cross-functional teams, as requested.
• Prepares for and provides microbiological expertise during regulatory inspections as required.
• Develops technical knowledge of site personnel in the area of microbiology
• Responsible for creating/improving training and training curricula related to microbiological hygiene and contamination prevention as needed.
  
  

Qualifications

Education:

• Minimum of a B.S. in Biology, Biochemistry, Microbiology, or a related discipline is required
• An MS or PhD in Biology, Biochemistry, Microbiology, or a related discipline is preferred
  
  

Required

Experience and Skills:

• Minimum of 6 years of experience is required
• Requires thorough knowledge of applicable cGMP requirements.
• Must have a detailed understanding of Large Molecule production processes and critical process steps in relation to contamination control.
• Experience on the shop floor in a pharmaceutical or biotechnological manufacturing environment.
• Advanced knowledge and understanding of regulatory requirements, including Safety, QA and QC functions, compliance requirements and experience in regulatory inspections.
• Must possess solid knowledge of routine and non-routine environmental testing and sampling methods, techniques and related equipment.
• Must be able to effectively don and wear required primary and secondary gowning materials (one-piece jumpsuits, head covers, gloves, overshoes, sterile frocks, etc.).
  
  

Preferred

• Knowledge of microbiological methods, including endotoxin, bioburden and microbial identification methods.
• Biochemical and chemical concepts, theories.
• Ability to deal with large amounts of complex information and often make critical decisions with limited information.
  
  

Other

LANGUAGE SKILLS:

• Must be able to communicate effectively, clearly and accurately in verbal and written English.
• Must be able to write accurate, grammatically correct reports, business correspondence and procedure manuals in English.
• Must be able to clearly and effectively present information and respond to questions from groups of managers and employees.
• Provide effective and timely communication to all levels in the organization, as appropriate, within and outside of department and to interact with external contacts.
• Ability to make effective and persuasive speeches and presentations on controversial or complex topics to top management, public groups and/or boards of directors.
  
  

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.