Comprehensive water, soil, vapor and air testing services

A clean and safe environment is a prerequisite for health and quality of life. Eurofins Environment Testing America provides market-leading laboratory testing, monitoring and consulting services to a wide range of industrial companies, environmental consultants, contractors, retailers and government authorities.

With a constant focus on regulatory compliance, customer service and data integrity, Eurofins Environment Testing America performs analysis of drinking water, groundwater, seawater, soil, air and tissue using state-of-the-art analytical methods to assess their quality and impact on health and the environment. We support a wide range of client types with virtually any testing needs related to:

• Department of Defense
• PFAS Analysis
• Metals & Metals Speciation
• Sediment and Tissue Testing
• Shale Oil and Gas Exploration
• Soil and Hazardous Waste Testing
• Specialty Services
• Vapor and Air Testing
• Water Testing
• Lead in Drinking Water Analysis

Industry: Environmental Services
Company Size: 1,001-5,000 employees

Eurofins Environment Testing (USA)

Savvy Admin PROD

Eurofins Scientific is a network of independent companies providing a unique range of analytical testing

services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.

Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.

With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients—including DoD, DOE, and municipalities—through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, radiochemicals, and more.

**Job Description**

The Laboratory Analyst prepares and analyzes environmental water samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Environment Testing Philadelphia, LLC’s Quality Assurance programs and SOPs.

**This position is ideal for students looking to gain environmental experience before they graduate with a degree in the Sciences. Environmental Science, Biology, Chemistry preferred.**

**Hours- Mon-Fri  1st shift.  Must live a commutable distance to Horsham, PA**

Positions are full-time, Monday-Friday 11 a.m. -7 p.m., with overtime offered as needed.

Compensation: $16-$18/hour (DOE)

**Temporary Lab Analyst responsibilities include, but are not limited to, the following:**

- Performs routine instrument maintenance including monitoring refrigerator and incubator temperatures daily to confirm that the readings are within SOP guidelines.

- Cleans and organizes the laboratory and workspaces daily to promote a clean, safe work environment and smoother flow of daily operations.

- Maintains and promotes safety and conducts all operations in a safe and environmentally compliant manner.

- Stocks and supplies inventory daily and assists with inventory of supplies to maintain proper quantity of materials to perform tasks appropriately.

- Retrieves samples from Sample Administration for analysis and ensures they are properly labeled.

- Prepares and analyzes water samples according to Standard Methods and EPA methods.

- Records and reports data, and notifies any unusual test occurrences to the supervisor.

- Performs other duties as assigned.

**Qualifications**

**Basic Minimum Qualifications:**

- High school diploma or equivalent

- Basic laboratory experience

- Authorization to work in the United States indefinitely without restriction or sponsorship

**The ideal candidate would possess:**

- Strong computer, scientific, and organizational skills

- Excellent communication (oral and written) and attention to detail

- Ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude

- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

- Ability to complete work within time and quality constraints

- Regular attendance and punctuality

- Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.

- Perform other duties as assigned

"All offers of employment are contingent upon a successful completion of a pre-employment drug screen and background check."

**Additional Information**

Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.

As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.  We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.

**We support your development! **Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

**We embrace diversity! **Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.

**Sustainability matters to us! ** At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler.

**Find out more in our career page: https://careers.eurofins.com/**

**Company description: ** ~~Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.~~

~~The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.~~

~~In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.~~

~~In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.~~

**We do not offer Visa Sponsorship for this role.**

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

**Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.**

Laboratory Analyst - Temporary - SUMMER - Environment Testing, Horsham PA

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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