Experienced Analyst, QC

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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.

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Titusville New Jersey United States of America

Job Description:

We are searching for the best talent for a Experienced Analyst QC to be based in Titusville NJ.

Purpose: We are seeking a highly skilled and experienced analyst whose primary responsibilities will include conducting comprehensive data reviews and approvals on stability testing in accordance with analytical methodologies. Additionally this individual should be prepared to perform select analytical tests independently adhering to established testing schedules to ensure seamless and efficient workflow. We require a candidate who demonstrates both exceptional productivity and meticulous attention to accuracy across all tasks

You will be responsible for:

• Review / Approve laboratory data in compliance with all applicable procedures standards and GMP regulations as well as all local state federal and international regulations and guidelines (FDA EPA DEA OSHA etc.).
• Maintain a safe work environment align with environmental health and safety regulations.
• Demonstrate a high level of understanding of analytical test methods with ability to independently implement and troubleshoot methods where required.
• Use electronic systems (LIMS MES LES Empower etc.) for execution and documentation of testing.
• Complete analytical method qualification validation and transfer with mentorship.
• Assist the execution of internal audits.
• Maintain individual training completion in a compliant state.
• Complete corrective and preventative actions (CAPA) as assigned.
• Support investigations and resolution of laboratory nonconformances.
• Make contributions to and occasionally lead continuous improvement teams. Interaction and involvement with global project teams.
• Provide input to functional laboratory meetings and take actions as a QC representative at cross-functional meetings.
• May occasionally assist the supervisor in prioritizing for the functional QC laboratory.
• Support the development and execution of CREDO action plans and initiatives.
• Trend analytical data generated by other analysts

• Bachelors degree and/or equivalent degree required; preferably in Science or related field.
• A minimum four (4) years of experience in a GMP-regulated science-related field.
• Detailed knowledge of analytical technologies used in the QC laboratory.
• Skilled in performing intermediate and advanced testing within the functional laboratory using HPLC and/or UPLC using the Empower software.
• Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to QC laboratory.
• Knowledge of compendial (USP EP JP etc.) requirements.
• Skilled technical writing skills.
• Ability to manage an individual project with mentorship from supervision/management.
• Ability to review testing documentation daily testing method transfer protocols
• Ability to read and interpret documents such as SOPs work instructions test methods and protocols.
• Proficient with using Microsoft Office applications (Outlook Excel Word and PowerPoint).
• Ability to make GMP laboratory decisions both independently and with occasional mentorship from QC Supervisor.
• Performs independent troubleshooting and root cause analysis skills. Works directly with supervision for resolution of complex issues.
• Demonstrates a high level of efficiency and proficiency in performing analytical testing in compliance with all regulations
• Experience with Karl Fischer analysis preferred.
• Experience with Dissolution apparatus and UV preferred.
• Experience authoring Standard Operating Procedures preferred.
• Utilize electronic systems (LIMS MES LES Empower etc.) for execution and documentation of testing preferred.
• This position will be located in Titusville NJ and may require up to 10% domestic or international travel.

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 & 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 () or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Analytical Reasoning Business Behavior Compliance Management Controls Compliance Cross-Functional Collaboration Innovation ISO 9001 Persistence and Tenacity Problem Solving Process Oriented Quality Auditing Quality Control (QC) Quality Control Testing Quality Standards Quality Systems Documentation Report Writing Technologically Savvy

The anticipated base pay range for this position is :

$79000.00 - $127650.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).

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

For additional general information on Company benefits please go to: - Experience:

Senior IC