Johnson & Johnson is hiring for a Quality Control Analyst I position in Titusville, New Jersey, offering an opportunity for a science and quality-control professional to join its Innovative Medicine organization.
The position focuses on analytical testing of stability samples and requires practical experience in a GMP-regulated, science-related environment. The successful candidate will work in a quality-control laboratory, performing analytical testing, supporting investigations, maintaining compliance documentation, and contributing to continuous-improvement activities.
The vacancy was posted on 27 August 2026 under requisition R-095600 and is listed as fully onsite. The employer currently anticipates that the posting will close on 4 September 2026, although Johnson & Johnson states that the period may be extended.
Background & Job Description
The Quality Control Analyst I position is part of Johnson & Johnson’s Quality function and Quality Control sub-function. The role is categorized as a professional position and is based in Titusville, New Jersey.
The primary purpose of the position is to conduct analytical testing of stability samples according to established testing schedules while ensuring that work is performed productively, efficiently, and in compliance with applicable quality standards.
The role forms part of Johnson & Johnson’s Innovative Medicine operations, where teams work on the development of medicines and treatments.
Key Responsibilities
The Quality Control Analyst I will support laboratory and quality-control activities across several areas.
Key responsibilities include:
- Performing analytical testing in accordance with procedures, standards, and GMP requirements.
- Following applicable FDA, EPA, DEA, OSHA, and other regulatory requirements.
- Maintaining a safe laboratory environment.
- Performing basic and intermediate analytical testing.
- Troubleshooting analytical methods when required.
- Using laboratory electronic systems such as LIMS, MES, LES, and Empower.
- Documenting laboratory testing accurately.
- Supporting analytical method qualification, validation, and transfer.
- Assisting with internal audits.
- Maintaining required training in a compliant status.
- Completing assigned corrective and preventive actions (CAPA).
- Supporting investigations into laboratory nonconformances.
- Participating in continuous-improvement teams.
- Contributing to global project teams.
- Participating in laboratory and cross-functional meetings.
- Providing input as a Quality Control representative.
- Assisting with prioritization of laboratory activities when required.
- Supporting CREDO action plans and initiatives.
The position therefore combines hands-on laboratory testing with documentation, compliance, investigation, and quality-improvement responsibilities.
Qualifications and Experience
Applicants are required to have at least one year of experience in a GMP-regulated, science-related field.
Candidates should also have basic knowledge of analytical technologies used in quality-control laboratories and practical experience performing basic and some intermediate testing using HPLC and/or UPLC.
Additional requirements include:
- Knowledge of current Good Manufacturing Practices (cGMP).
- Basic understanding of compendial requirements such as USP, EP, and JP.
- Basic technical-writing ability.
- Ability to manage an individual project with appropriate mentorship.
- Ability to read and interpret SOPs, work instructions, test methods and protocols.
- Proficiency with Microsoft Office applications, including Outlook, Excel, Word and PowerPoint.
- Ability to make appropriate GMP laboratory decisions independently and with occasional guidance.
- Basic troubleshooting and root-cause-analysis skills.
Education and Technical Skills
The supplied vacancy does not specify a particular degree in its published qualification section. Instead, it emphasizes relevant experience in a GMP-regulated science environment and technical laboratory competencies.
Applicants should therefore carefully review the official application requirements and ensure that their educational and professional background supports the analytical laboratory responsibilities of the role.
Experience with HPLC or UPLC, laboratory information-management systems, and quality-control documentation is particularly relevant.
Knowledge of GMP requirements is also important because laboratory testing must be conducted in accordance with established procedures and regulatory standards.
Quality Control Responsibilities
Quality control is central to the position.
The successful candidate will be expected to conduct analytical testing accurately while following established procedures and applicable regulatory requirements. The position also involves investigating laboratory nonconformances, completing CAPA activities, and contributing to audits and continuous-improvement initiatives.
This means applicants should be comfortable working in a structured laboratory environment where documentation, compliance, and consistency are essential.
The ability to identify problems, conduct basic troubleshooting, and contribute to root-cause analysis will also be valuable.
Salary and Benefits
Johnson & Johnson lists an anticipated base-pay range of $54,000 to $87,400 per year for the Quality Control Analyst I position. Actual compensation may vary according to factors such as experience and other applicable considerations.
The vacancy also states that eligible employees may participate in the company’s consolidated retirement plan, including pension and 401(k) savings arrangements, as well as a long-term incentive programme.
Listed time-off benefits include vacation, sick time, holidays, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time off, subject to applicable company policies and eligibility requirements.
Work Location and Employment Details
| Category | Details |
|---|---|
| Employer | Johnson & Johnson Services, Inc. |
| Position | Quality Control Analyst I |
| Function | Quality |
| Sub-function | Quality Control |
| Location | Titusville, New Jersey, USA |
| Work pattern | Fully onsite |
| Requisition | R-095600 |
| Date posted | 27 August 2026 |
| Anticipated closing date | 4 September 2026 |
| Experience | Minimum 1 year in a GMP-regulated science field |
| Key laboratory skills | HPLC and/or UPLC |
| Salary range | $54,000–$87,400 |
The official listing identifies Titusville, New Jersey, as the job location and confirms that the work pattern is fully onsite.
Important Note About the Advertisement
The supplied headline describes the opportunity as “Male Only.” However, the official Johnson & Johnson vacancy provided with the job details does not state a male-only eligibility requirement. Instead, Johnson & Johnson’s official posting states that it is an equal-opportunity employer and that qualified applicants receive consideration without regard to protected characteristics.
For accuracy and fairness, applicants should rely on the official employer’s eligibility requirements rather than assuming that the “Male Only” wording in a third-party advertisement forms part of the official vacancy criteria.
How to Apply
Interested candidates can apply through the official Johnson & Johnson Careers website. The vacancy includes an Apply Now option and is listed under requisition R-095600.
Apply for the Quality Control Analyst I position at Johnson & Johnson
Applicants should prepare an updated CV highlighting their laboratory experience, GMP knowledge, HPLC/UPLC experience, analytical testing capabilities, technical-writing skills, and familiarity with laboratory systems.
Because the stated anticipated closing date is 4 September 2026, candidates interested in the opportunity should check the official listing promptly. Johnson & Johnson notes that the posting may remain available longer if the company extends the closing period.
Final Words
The Johnson & Johnson Quality Control Analyst I opportunity provides an opening for an experienced laboratory professional to work within the company’s Quality Control function in Titusville, New Jersey.
The position requires at least one year of GMP-regulated science experience, knowledge of analytical laboratory technologies, and practical testing experience using HPLC and/or UPLC. Candidates should also understand cGMP requirements, laboratory documentation, and basic troubleshooting and root-cause analysis.
With an advertised base-pay range of $54,000–$87,400, the role may appeal to professionals seeking to develop their careers in pharmaceutical quality control and analytical laboratory operations.
Applicants should review the official vacancy carefully and apply through Johnson & Johnson’s careers platform before the advertised closing date.
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