Manager Quality Control Microbiology Lab - 2407017739W

Manager Quality Control Microbiology Lab - 2407017739W

12 Mar 2024
Pennsylvania, Lititz, 17543 Lititz USA

Manager Quality Control Microbiology Lab - 2407017739W

Manager Quality Control Microbiology Lab - 2407017739WDESCRIPTION/RESPONSIBILITIES:

Description

Kenvue is currently recruiting for:

Manager Quality Control Microbiology LabThis position will report into the Quality Director, and is based in Lititz, PA.Role reports to: Quality DirectorLocation: 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 requirementsKey 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 s rong organizational and analytical skill to comprehend technical data/information and convert them into value-added actionable items is required

10 % Travel is requiredDesired 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 desirableWhat'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/regionNote: 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.

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