Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.  

Through world class people, process, and technology, Astrix works with clients to fundamentally improve business & scientific outcomes across many domains including the laboratory, clinical & regulatory, pharmacovigilance, R&D, and manufacturing. 

Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of strategic, application & platform, data transformation & analytics, change management, and staffing services designed to deliver immediate value to clients and solve their most complex technical and staffing challenges.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Astrix

Savvy Admin PROD

Pay Rate Low: 40 | Pay Rate High: 45

Seeking a Chemist to join a world leader in science. Opportunity to join an R&D Analytical Characterization team, supporting chromatography and wet chemistry testing of materials used in medical/surgical products. This role focuses on analyzing small organic compounds, additives, degradation products, and impurities in complex polymer systems.

Key Responsibilities

- Perform analytical testing using GC, Headspace GC, and U/HPLC-UV.

- Conduct full workflows including sample preparation, method execution/qualification, data analysis, and reporting.

- Investigate and report issues such as OOS/OOT results, instrument problems, and lab deviations.

- Troubleshoot and maintain analytical instruments.

- Document work in compliance with FDA/ICH standards and internal procedures.

- Communicate results clearly through written reports and presentations.

- Support preparation of technical reports and documentation

**Qualifications**

- BS, MS, or PhD in Chemistry (Analytical, Polymer, Organic) or related field

- ~1–2+ years of relevant experience (depending on degree level)

- Familiarity with medical device or regulated environments preferred

- Strong foundation in analytical chemistry principles

- Hands-on experience with GC and HPLC instrumentation

- Experience with method development/validation (preferred)

Analytical Chemist

At Johnson & Johnson, we believe health is everything. As a focused healthcare company, with expertise in Innovative Medicine and MedTech, we’re empowered to tackle the world’s toughest health challenges, innovate through science and technology, and transform patient care.  

All of this is possible because of our people. We’re passionate innovators who put people first, and through our purpose-driven culture and talented workforce, we are stronger than ever. 

Learn more at https://www.jnj.com. Community Guidelines: http://www.jnj.com/social-media-community-guidelines

Industry: Hospitals and Health Care
Company Size: 10,001+ employees

Johnson & Johnson

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.

**Job Function**

Technology Enterprise Strategy & Security

**Job Sub Function**

Security & Controls

**Job Category**

People Leader

**All Job Posting Locations:**

Raritan, New Jersey, United States of America

**Job Description**

**Employer: ** Johnson & Johnson Services, Inc.

**Job Title: ** App Security Manager

**Job Code: ** A011.7393

**Job Location: **Raritan, NJ

**Job Type: ** Full-Time

**Rate of Pay: ** $147,000 - $165,000

**Job Duties: ** Design and deliver security solutions for S/4 HANA SAP. Develop and implement Application Data Security policies and procedures. Assess functional requirements and provide recommendations per Application Security guidelines and compliance standard methodologies. Translate functional specifications into a technical design for data-level security. Responsible for MedTech S4 Security Support in accordance with Global Security Strategy and Administration. Work across multiple BT, Architecture, PL and TS groups to define and deliver innovation solutions. Drive business value from a security perspective with respect to core internal IT security solutions. Craft and build security groups and permissions. Serve as primary point of contact for ISRM, vendors, and enterprise platform owners. Responsible for user administration with Active Directory or Identity Access Management. Identify risks and compliance issues by running segregation of duties checks. Work with the Support Lead to drive issue resolution and proper partner concern. Introduce delivery automation processes (testing, release, development control, etc.). Participate in continuous process improvement initiatives, and identify opportunities for efficiency, scalability and/or cost improvements. Apply enterprise data level security and reporting security for new technology solutions, and work with Product Owners to ensure the development of a product vision, roadmap, and backlog. Drive scaled Agile security delivery, working in partnership with Product Owners, Product Analysts, and Solution / Data Engineers to manage risk in the backlog. Support multiple project life cycles concurrently including different iterations of testing, project Go-Lives, cutover and Hypercare. Facilitates internal and external audits as necessary.

May telecommute per company's policies (hybrid).

**Requirements: ** Employer will accept a Bachelor's degree in Information Technology, Computer Science, Business Administration or related field and 4 years of experience in the job offered or in an App Security Manager-related occupation.

This job posting is anticipated to close on **5/26/2026.**

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 contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

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.

**Benefits**

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

- This position is eligible for benefits to include medical, dental, vision and time off, as well as any others as provided for in the applicable Collective Bargaining Agreement.

- For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

**Required Skills**

**Preferred Skills: **

App Security Manager

At Johnson & Johnson Innovative Medicine, we are leading where medicine is going. The experiences of patients around the world inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science with compassion, we confidently address the most complex diseases of our time and develop the potential medicines of tomorrow. We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way. https://bit.ly/3reuMvK

Industry: Pharmaceutical Manufacturing
Company Size: 10,001+ employees

Johnson & Johnson Innovative Medicine

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.

**Job Function**

Product Safety

**Job Sub Function**

Product Safety Risk Management

**Job Category**

Scientific/Technology

**All Job Posting Locations:**

Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America

**Job Description**

**About Innovative Medicine**

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

**About Oncology**

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities for finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

**Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):**

**United Kingdom **- Requisition Number: R-061721

**Belgium ** - Requisition Number: R-062304

~~Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.~~

**We are searching for the best talent for an Associate Director, Safety Analysis Scientist, located in Raritan, NJ; Titusville, NJ; or Horsham, PA. This is a hybrid position that requires you to be on site three days a week.**

**Purpose**

The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products. The AD SAS, in partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.

The AD SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.

The AD SAS will assist the Medical Safety Officer (MSO) with activities related to the SMT and with contributions to key safety and clinical documents.

The AD SAS will have in-depth product knowledge, will serve as product point of contact, and will provide training to, and oversight of deliverables prepared by, other team members as needed (for complex reports).

The AD SAS will function with a high level of independence, with minimal guidance from the Director, Safety Analysis Scientist (SAS) Therapeutic Area Lead (TAL), be able to link discussions to content, and consistently deliver high quality results with minimal guidance.

The AD SAS will quickly build alliances and be able to independently influence other safety partners to shape strong decisions/outcomes.

**You Will Be Responsible For**

- Lead safety evaluations including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.

- Ensure high quality safety evaluations and reports with minimal comments from stakeholders and minimal revisions required.

- Provide input and review of key regulatory or clinical documents as appropriate.

- Demonstrate leadership in the SMT and support the MSO.

- Support SMT activities (e.g., preparing and presenting data, compiling meeting minutes, updating signal tracking information).

- Lead proactive safety data reviews, if applicable and form a safety position across Global Medical Safety (GMS) which can be leveraged for aggregate safety reports.

- Provide support for Health Authority interactions regarding safety and risk management, both written and verbal.

- Assume responsibility for novel projects, create value and innovate without defined processes. May seek guidance from Directors (i.e., SAS TAL) for complex projects.

- Lead cross-functional training of relevant stakeholders.

- Act as product or process Subject Matter Expert (SME) for audits/inspections.

- Participate in, or lead, department and/or cross-functional initiatives.

- Explore innovative ways of presenting data, preparing reports, and improving efficiencies within the programs they own.

- Assist Directors in the creation, review and implementation of controlled documents and other related tools.

- Management of unscheduled reports within the Aggregate Report Calendar.

- Management activities within smaller Therapeutic Areas, as applicable.

- Line-management of contractor positions within the team, as applicable.

- Act as backup to TAL as needed (e.g., Director SAS TAL is unavailable).

- Oversight of deliverables by other team members (e.g., complex reports), as needed

**Qualifications / Requirements**

**Education:**

- Bachelor’s Degree Required: Healthcare-related or Biomedical Science (11+ years industry experience or equivalent).

- Advanced Degree Preferred: Healthcare-related or Biomedical Science (8+ years industry

- experience or equivalent).

**Experience**

**Required:**

- Medical writing or Pharmacovigilance (PV) experience required.

- Working knowledge of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements.

- Ability to understand and analyze complex medical-scientific data from a broad range of disciplines.

- Ability to interpret and present complex data to determine benefit-risk impact.

- Excellent English verbal and written communication skills.

- Ability to effectively interact with stakeholders, including business partners.

- Ability to work in a matrix environment, proven leadership skills.

- Ability to plan work to meet deadlines and effectively handle multiple priorities.

- Proficiency in Microsoft applications (e.g., Word, Excel, and PowerPoint).

- Ability to independently influence, negotiate and communicate with both internal and external customers.

**Preferred**

- Clinical experience preferred.

- Oncology experience preferred.

~~The anticipated base pay range for this position in the US is $137,000 to $235,750. The compensation and benefits information set forth in this posting applies to candidates hired in the United States.~~

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

**Employees Are Eligible For The Following Time Off Benefits**

- Vacation – up to 120 hours per calendar year

- Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year

- Holiday pay, including Floating Holidays – up to 13 days per calendar year

- Work, Personal and Family Time - up to 40 hours per calendar year

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits

This job posting is anticipated to close on March 12th, 2026. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

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 and 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 (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

**Required Skills**

**Preferred Skills:**

Clinical Operations, Compliance Management, Compliance Risk, Data Reporting, Medicines and Device Development and Regulation, Mentorship, Presentation Design, Quality Control (QC), Research Ethics, Researching, Risk Management, Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Tactical Planning, Technical Credibility, Technical Writing

Associate Director, Safety Analysis Scientist

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