Job Information
J&J Family of Companies Manager Quality Control Microbiology Lab in Lititz, Pennsylvania
Manager Quality Control Microbiology Lab - 2407017739W
Description
Kenvue is currently recruiting for:
Manager Quality Control Microbiology Lab
This position will report into the Quality Director, and is based in Lititz, PA.
Who we are
At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here (https://www.youtube.com/watch?v=XhsbOsBiX_M) .
Role reports to: Quality Director
Location: Lititz, PA.
Travel %: 10%
Pay: $99,000 to $170,200.
What you will do
The Manager Quality Control Microbiology Lab is responsible for managing and coordinating the activities of the Microbiology Laboratory personnel engaged in the testing and evaluation of raw materials, finished products, USP Purified Water and environmental monitoring samples. Partners with other groups to align with production schedules, plant resources and corporate requirements. Ensures that Microbiology Laboratory activities are performed in full compliance with cGMPs and safety requirements
Key Responsibilities
Mentor, coach, and develop the Microbiology Laboratory staff.
Evaluate performance and provide opportunities for growth.
Develop an environment of continuous Microbiology Laboratory improvement.
Communicate department objectives and metrics and measure results.
Participate in planning and implementing changes in testing, methodology and instrumentation to support the business and maintain compliance with cGMPs.
Ensure development of sampling and testing schedules to support the business, in full compliance with cGMPs.
Oversee investigation of questionable and out-of-alert results originating from laboratory sources, and ensure that appropriate corrective actions are implemented, as needed.
Participate in Investigation and CAPA activities associated with microbiological activities.
Actively endeavor to reduce microbiological-related Investigations.
Provide data, support and resources to remediate or improve the microbiological environment at the Site.
Escalate issues as necessary to Management.
Ensure full cGMP and safety compliance in the Microbiology Laboratory.
Prepare, review and/or approve written reports, SOPs and other types of communication.
Prepare and administer budget.
Ensure quality and compliance through actions by:
All employees
Attending GMP training on the schedule designated for the role.
Adhering to strict compliance with procedures applicable to the role.
Exercise the highest level of integrity in the tasks that are performed.
In a timely and prompt manner, identifying, reporting and seeking correction for deviations noted in the workplace.
Embracing a behavior of employee involvement and commitment to doing the job right the first time.
People Managers
Ensuring employees under the scope of responsibility are trained in required procedures for the execution of their role and remain current with training requirements during the year.
Promoting an environment of employee involvement and inclusion in the workplace.
Seeking prompt identification, reporting and correction of deviations in the workplace as noted by employees.
Actively participate in regulatory inspections and audits.
Qualifications
What we are looking for
Required Qualifications
Bachelor's degree in technical, scientific, or related/equivalent discipline is required
10 years responsibility and experience in a GMP product manufacturing plant environment required including a broad and deep working knowledge of the OTC drug product operating functions of quality and compliance, supply chain, material supply and material handling and control, product manufacturing and product packaging is required.
An understanding and application of current Good Manufacturing Practices experience is (cGMP) and Agency compliance expectations is required
Demonstrated leadership skills to achieve results through others- with and without direct authority is required
An ability to develop and implement strategy/initiatives based on required needs is required
Demonstrated strong organizational and analytical skill to comprehend technical data/information and convert them into value-added actionable items is required
10 % Travel is required
Desired Qualifications
Masters Degree is desirable
Prior experience with regulatory inspections is desirable
Experience with Six Sigma Process Excellence tools, training and/or certification is desirable
Demonstrated competency as a Supervisor or Team Leader is desirable
Energetic, with strong interpersonal, organizational and communication skills is desirable
Ability to perform in a leadership role and to effectively manage people is desirable
Self Motivated is desirable
What’s in it for you
Annual base salary for new hires in this position ranges from $99,000 to $170,200 . This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
Competitive Total Rewards Package
-
+
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups
This list could vary based on location/region
Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
#LI-LB2
Primary Location NA-US-Pennsylvania-Lititz
Job Function Quality Control
Organization : Johnson & Johnson Consumer Inc.
Req ID: 2407017739W