Supervisor Quality Control

Johnson & Johnson Innovative Medicine•Malvern, PA

About The Position

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 jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Manages all aspects of Quality Control (QC), in support of designated Innovative Medicine Supply Chain (IMSC) sites and supports Malvern Clinical Operations in full compliance with established cGMP and IMSC requirements. Activities include managing in-process testing, raw material testing, environmental monitoring sample testing, utility sample testing, validation sample testing, stability sample testing, method transfer and method validation sample testing, testing of reagents, media, and buffers, and other samples as appropriate. Develops and implements long-term strategy, and execution of Quality Control programs. Ensures department staff complies with all J&J, IMSC and government-issued environmental, health, safety, quality and regulatory policies and guidelines, including FDA, EMEA and regulatory bodies of any applicable non-EU countries This role is responsible for carrying out supervisory responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include interviewing, hiring, training employees, appraising performance, rewarding and disciplining employees, addressing complaints and resolving conflict.

Requirements

Demonstrate Ability to quickly process complex information and often make critical decisions with limited information.
Maintain a high level of strategic thinking to apply over multiple focus areas under scope of work.
Manage multiple priorities daily while being flexible and responsive to frequently shifting priorities.
Demonstrate influencing skills, partnering and collaboration skills, analytical skills, and good oral and written presentation skills.
Demonstrate ability to work across organizational boundaries.
Serve as a role model for making Credo-based decisions.
Create a trusting, collaborative, and ethical work environment.
Maintain the highest standards of quality, compliance, and accountability.
Champion programs and initiatives that support our environment and communities.
Think analytically and acts decisively.
Applies knowledge of Quality Control best practices and raises issues that may impact organizational objectives.
Complete processes to ensure the internal organization's alignment with overall quality priorities.
Implements formal escalation processes to surface issues in QC processes, regulatory compliance, and quality systems.
Maintain advanced knowledge/experience with regulatory requirements, policies and guidelines.
Maintain advanced knowledge of Laboratory Testing , Laboratory systems and current Good Manufacturing Practices (cGMP) with ability to identify/remediate gaps in processes or systems.
Understanding in responsibility of people management, development, and supervision.

Responsibilities

Ensuring adequate training (skills-based, cGMP and safety) of management and associates within the department.
Raw material, in-process, environmental/utility, product release, and stability testing.
Investigation of laboratory non-conformances (events, deviations, and invalid assays).
Maintenance, calibration and qualification of laboratory instruments and equipment.
Test method verification, qualification, validation and/or transfer activities in the QC laboratories.
Process Performance Qualification and Continued Process Verification activities associated with QC laboratory testing.
Material evaluation/testing as part of the Supplier Material Qualification (SMQ) process.
Provides expertise in troubleshooting complex laboratory issues and demonstrates strong reasoning skills in support of ongoing laboratory investigations.
Maintains detailed knowledge of industry guidelines/trends, regulatory requirements, and applicable pharmacopeia while remaining current in on-the-job training requirements.
Collaborates with Quality Assurance, Manufacturing, Technical Operations, Engineering and Maintenance to support business needs.
Contributes to global strategies related to QC laboratories which align with compliance and business objects as well as the overall J&J vision.
Carries out duties in compliance with all local, state and federal regulations and guidelines including FDA, EPA, and OSHA.
Complies with all company and site policies and procedures.
Manages departmental budget and resources; prepares staffing plans.
Makes adjustments to roles and responsibilities of department to meet business needs.
This role is responsible for carrying out supervisory responsibilities in accordance with the organization’s policies and applicable laws.
Responsibilities include interviewing, hiring, training employees, appraising performance, rewarding and disciplining employees, addressing complaints and resolving conflict.
Reviews and/or approves quality documents (standard operating procedures, specifications, test methods, work instructions, risk assessments, technical/validation protocols and reports, etc.), non-conformance investigations, CAPA, and change controls associated with the QC laboratories.
Supports internal and external audits, including external contract laboratories and GMP service providers, where required.
Escalates potential product quality issues.
Analyzes laboratory performance and quality data for quarterly site management and annual product reviews.
Provides oversight for raw material reduced testing programs.
Supports the Janssen Biotherapeutics Discovery and Supply (BTDS) group through; Characterization and/or release testing for projects related to early development, clinical, and commercial products.
Co-validation and/or transfer of new analytical test methods.
Provides input to product quality complaint investigations.
Prepares for and provides QC expertise during Health Authority inspections as required.
Influences senior leaders, and external colleagues/partners, across disciplines as well as globally in driving, and aligning, strategic and operational activities between business units/functions.
Monitors departmental metrics and delivers reports to senior management, as necessary.
Manages strategic capital projects.
Supports and leads global initiatives and implementation at the local level.
Allocating resources and confirming alignment of changes with site strategies in the change management processes within functional areas.

Benefits

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year