Encompass Health is the largest owner and operator of rehabilitation hospitals in the United States. With a national footprint that includes 158 hospitals in 37 states and Puerto Rico, the Company provides high-quality, compassionate rehabilitative care for patients recovering from a major injury or illness, using advanced technology and innovative treatments to maximize recovery. Encompass Health is ranked as one of Fortune’s 100 Best Companies to Work For and Modern Healthcare’s Best Places to Work in Healthcare.

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

Encompass Health

Savvy Admin PROD

**Valued For Your Human Resource Skills**

Are you an experienced Human Resources professional seeking a dynamic role? Join our team as a Human Resources Coordinator, where your expertise will be pivotal in streamlining HR functions and providing essential support to employees and managers. Your duties span seamless communication, recruitment assistance, employee records management, and enhancing overall HR efficiency. As a coordinator, you'll spearhead screening and interviews, oversee FMLA for benefits, and deliver exceptional customer service. Your role also involves preparing for surveys and contributing to HR projects, requiring robust organizational skills and computer proficiency.

**A Glimpse into Our World**

At Encompass Health, you'll experience the difference the moment you become a part of our team. Working with us means aligning with a rapidly growing national inpatient rehabilitation leader. We take pride in the growth opportunities we offer and how our team unites for the greater good of our patients. Our achievements include being named one of the "World's Most Admired Companies" and receiving the Fortune 100 Best Companies to Work For Award, among other accolades, which is nothing short of amazing.

**Starting Perks And Benefits**

At Encompass Health, we are committed to creating a supportive, inclusive, and caring environment where you can thrive. **From day one **, you will have access to:

- Affordable medical, dental, and vision plans for both full-time and part-time employees and their families.

- Generous paid time off that accrues over time.

- Opportunities for tuition reimbursement and continuous education.

- Company-matching 401(k) and employee stock purchase plans.

- Flexible spending and health savings accounts.

- A vibrant community of individuals passionate about the work they do!

**Become the Human Resources Coordinator you always wanted to be**

- Support recruitment by screening resumes and identifying candidates.

- Manage FMLA processes.

- Provide outstanding customer service to employees and managers, addressing their needs effectively.

- Assist in federal, state, and Joint Commission survey preparedness activities.

- Contribute to special HR projects and serve as a project coordinator when necessary.

**Qualifications**

- Professional in Human Resources (PHR) and/or SPHR certification preferred.

- BA or BS degree in Personnel Administration, Hospital Administration, Business Administration, or a related field preferred. Experience may substitute for four year degree on a year for year basis.

- One to three years of experience in Human Resources, preferably in healthcare.

- Proficiency in Microsoft Office Suite (Excel, Word, Publisher, PowerPoint) preferred.

**The Encompass Health Way**

We proudly set the standard in care by leading with empathy, doing what's right, focusing on the positive, and standing stronger together. Encompass Health is a trusted leader in post-acute care with over 150 nationwide locations and a team of 36,000 exceptional individuals and growing!

At Encompass Health, we celebrate and welcome diversity in our inclusive culture. We provide equal employment opportunities regardless of race, ethnicity, gender, sexual orientation, gender identity or expression, religion, national origin, color, creed, age, mental or physical disability, or any other protected classification.

We're eagerly looking forward to meeting you, and we genuinely mean that. Join us on this remarkable journey!

Human Resources Coordinator

IT Consulting at its Best!
Quantum Integrators is an international strategy and business consulting group whose mission is to help clients create and sustain competitive advantages. As a truly client-focused firm, our highly trained and experienced consultants consider it their mandate to help your organization achieve what we call a “Quantum State”, optimizing your ERP system. The accomplishments noted within the accompanying people will illustrate the value and vision that we can bring to your Company.

Innovation is driven by technology which in turn is driven by business needs. Our job is to help you achieve corporate success by helping you deploy enterprise solutions bringing together interrelated business processes under a standard architecture that helps the enterprise become more efficient, productive, and agile in response to changing business conditions.  	
Please visit us at www.QuantumIntegrators.com to realize what we do and how we can add value to your ERP investment.

Robotic Process Automation (RPA) at Quantum:
We have delivered RPA solutions to various clients spanning almost the entire market domain including Healthcare and Pharmaceutical, Manufacturing, Staffing and Recruiting, Financial, and Banking.
Being a direct partner of UiPath and with a highly experienced RPA development team; both onshore and offshore, we have successfully automated some of the complex business processes including Automation solutions for ERP - SAP Systems, and other Secure Remote Applications.
We can provide automation POC to showcase our capabilities.

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

Quantum Integrators

Role: SAP BDC Engineer

Long Term Contract

The location can be either of the following 2 listed below:-

1250 S Collegeville Rd, Collegeville, PA 19426

410 Blackwell St. ~~Durham ~~, NC 27701

(Delta Sharing with Governance/Automation blended capability)

• SAP DBC Delta Sharing and Unity Catalog integration

• Data governance, including RBAC, classification, and auditability

• Automation using Terraform, APIs, and CI/CD pipelines

• Logging, monitoring, and compliance frameworks

• UAT and production validation support

**Expected Outcomes **

- Fully governed SAP BDC → Delta Share → Unity Catalog integration

- Audit-ready, GxP-compliant platform

- Automated self-service provisioning framework

- Successful UAT-to-production rollout across business units

**Regards, **

**Jagannath Gaddam **

jagannath.gaddam@quantumIntegrators.com

**www.QuantumIntegrators.com **

SAP BDC Engineer

About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. 

For more information, please visit www.thermofisher.com.

Industry: Biotechnology Research
Company Size: 10,001+ employees

Thermo Fisher Scientific

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

Join us as a Scientist!

This is a fully onsite role based at our customer’s site in **Collegeville, PA.**

We welcome applicants from all locations within the US.

Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

**Summarized Purpose**

Our team is searching for a Scientist who will be responsible for the analysis of biological samples using Liquid-Chromatography and Mass Spectrometry to deliver PK and PD endpoints for clinical studies across the client portfolio.

**Essential Functions:**

- Perform analysis of drugs, metabolites, and biomarkers in biological samples to applicable standards using defined analytical methods.

- Produce written analytical methods, reports, and report contributions.

- Ensure that work is performed in compliance with the relevant regulations (primarily GCP), with procedures guided by applicable government regulations, and relevant SOPs.

- Handle human biological samples and perform experimental work in accordance with HBSM, safety and data integrity guidelines.

**Education and Experience: ******

- BS in Chemistry, Biochemistry or related discipline with 2 years of related experience

- Basic knowledge and hands-on experience with LC/MS and/or quantitative bioanalytical methods.

- Understanding of regulatory requirements for GLP and GCP analytical activities.

- Excellent computer skills for communication and report writing

**In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.**

**Knowledge, Skills, and Abilities:**

- Experience with analysis and reporting of preclinical or clinical PK data.

- Experience handling of human biological samples.

- Proven experience and ability to troubleshoot methodological issues

- Experience utilizing laboratory information management systems for daily job functions.

- Highly motivated team player with a proactive attitude, excellent organizational skills and a demonstrated ability to interact effectively within a multi-disciplinary team

Working Conditions and Environment:

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements:

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Scientist, Mass Spec

We share stories from our team sharing real life challenges, struggles and successes they have. We share their experience before, during, and occasionally after Vector.

We have the opportunity to show our American-Made, Forever Guaranteed product CUTCO®. Established in 1981, Vector Marketing Corp. is the sole distributor of CUTCO®. More than 15 million customers in the US and Canada enjoy CUTCO® products in their homes every day.

The stories we share are from real people, just like you, who started selling our product and now have accomplished great things. Whether they are working part-time or full-time hours, they share how you too can benefit from working at Vector.

Industry: Manufacturing
Company Size: 501-1,000 employees

Vector Marketing

Vector Marketing is looking to fill part-time sales positions right away. Request an interview today and start work within the week.

**What are the position details?**

Our reps sell Cutco products through one-on-one appointments, explaining the products, and placing any orders. Previous work experience isn't required, we are just looking for people who enjoy working with others.

Reps are paid $25.00 base-appt that isn't based on sales or results, but they can earn more based on commission. If they have an off week, they still get paid for the work they did, but can earn more based on performance.

We help reps create a schedule that works best for them. Some work as much as possible, some part time, and others are just looking to make some extra income around their classes, other jobs, and family obligations. Summer work schedules are available for anyone looking for seasonal work.

Our Cutco products are used in the kitchen and some outdoor tools as well. Previous knowledge about home goods, sales, or work experience is not needed. We are just looking for people who enjoy working with others.

We've been training people to do well for over 40 years. Even if someone doesn't stay with us long term - the sales, networking, and communication skills they build are needed for every field. Reps work locally after training, meetings and training are held in the office.

**What are the basic requirements?**

-  Enjoys working with others

-  All ages 18 + or 17 and a 2026 Highschool Graduate

-  Some conditions apply

-  Able to interview within the week

-  Willing to learn and apply new skills

**Who would do well here?**

People who have done well with us have had experience in all different lines of work - retail, fast food, cashier, grocery store clerk, administrative assistant, receptionist, server, landscape, warehouse worker, and in just about any field you can imagine. We also welcome applicants who haven't had any work experience. If they have a positive attitude and enjoy working with people, they can do well here.

If you think you would be a great fit for our sales team, fill out contact information and a receptionist will send you a text about setting up a virtual interview with a manager. We encourage applicants of all ages and experience, as we do not discriminate on the basis of an applicant's age.

Flexible Work - Entry Level Sales Representative - Paid Weekly

For 85 years, PerkinElmer has pushed the boundaries of science in our food, industrial, life science and environmental markets. In addition to innovative laboratory technologies, our OneSource services division delivers a highly trained, experienced, and collaborative team of service engineers with solutions scalable and customizable to serve laboratory needs. 
We’ve always pursued science with a clear purpose – to help our customers achieve theirs. Our expert team brings technology and intangibles, like creativity, empathy, diligence, and a spirit of collaboration, in equal measure, to fulfill our customers’ desire to work better, innovate better, and create better. 

PerkinElmer is a leading, global provider of technology and service solutions that help customers measure, quantify, detect, and report in ways that help ensure the quality, safety, and satisfaction of their products.  

Science with Purpose. Learn more at www.perkinelmer.com.

Industry: Biotechnology Research
Company Size: 5,001-10,000 employees

PerkinElmer

**Job Description Summary**

The Associate Laboratory Technician plays a critical role in maintaining the daily operations of the laboratory. This position ensures that lab spaces are clean, organized, and fully stocked with necessary materials and that equipment is properly maintained and ready for use. The technician supports scientists by preparing materials, managing inventory, and assisting with basic technical tasks.

**Job Responsibilities**

- Communicate clearly and professionally with customers, both verbally and in writing.

- Collaborate with team members to complete routine tasks that ensure lab and equipment readiness.

- Monitor and replenish laboratory supplies, reagents, and consumables.

- Prepare and set up equipment and materials for experiments or instructional labs.

- Clean and sterilize glassware, instruments, and workspaces.

- Perform routine maintenance and calibration of laboratory equipment.

- Receive, label, and store incoming materials.

- Maintain accurate inventory records and report low stock or equipment issues.

- Ensure compliance with lab safety protocols and assist with safety inspections.

- Dispose of chemical and biological waste in accordance with regulations.

- Provide basic troubleshooting support and guidance on equipment use.

- Escalate issues promptly to supervisors.

- Support team goals and contribute to a collaborative work environment.

- Escort and coordinate with vendors visiting lab areas.

- Follow documented Standard Operating Procedures (SOPs) for lab tasks.

- Assist with service work orders and coordinate maintenance and service events with scientists and key personnel.

- Support communication efforts, including posting signs and forwarding relevant emails.

Note: This job description does not restrict management’s right to assign or reassign duties and responsibilities at any time.

**Critical Skills**

- Takes ownership of tasks and drives them to completion

- Excellent interpersonal and communication skills with a customer-first mindset

- Strong attention to detail required

- Strong written and verbal communication skills

- Ability to follow oral and written instructions accurately

- Intermediate proficiency in Microsoft Office (Outlook, PowerPoint, Word, Excel)

**Basic Qualifications**

- High School Diploma or equivalent

- 1–2 years’ experience in a customer-facing role

**Preferred Qualifications**

- 2+ years of experience in a scientific or laboratory environment

- Associate degree or professional certification in a relevant field (e.g., Project Management, Six Sigma, Business Administration, Supply Chain)

- Basic understanding of GLP/GxP and experience in a compliance-driven environment

- Familiarity with 5S principles (Sort, Set in Order, Shine, Standardize, Sustain)

- Knowledge of chemical handling and safety practices

- Basic understanding of Occupational Health and Safety standards

- Ability to read and interpret chemical labels and safety signage

- Familiarity with Good Documentation Practices (GDP)

**Working Environment**

- Must be able to work in a laboratory, controlled environments requiring personal protective equipment (e.g., lab coat, safety glasses, etc.)

- Job pace may be fast and job completion demands may be high

- Must be able to remain in a stationary position more than 25% of the time

- Occasionally move between labs, corridors, adjoining rooms, and buildings onsite

- Frequently operate on instruments, objects, tools or controls, requiring bending, squatting, stretching, and reaching

- Occasionally move or lift up to 25 pounds (potential for occasional lifting of up to 50 pounds)

- Must have vision abilities including close range, distance, color, peripheral vision, depth perception, and focus adjustment

- Occasionally operate a computer and other office machinery

- May handle hazardous waste according to regulations

- Potential exposure to lab-based hazards including temperature extremes, biological materials, and hazardous chemicals

- May require Medical Clearance, Respiratory Protection Training, and Fit Testing

~~The annual compensation range for this full-time position is $50,960. The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training. ~~

Associate Lab Technician

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

Role: Scientist, Formulations

This is a fully onsite role based at our customer’s site in Collegeville, PA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to demonstrate the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

As a Scientist supporting the Pharm Dev Steriles in our client's Pharmaceutical R&D, you will have the opportunity to apply technical skills and expertise to develop drug product formulations and associated manufacturing processes as part of a matrix technical team. You will also use creative thinking to drive drug development of a variety of sterile product dosage forms

**Key Responsibilities:**

- Completes pre-formulation, formulation and process development activities based on established protocols and procedures

- Assists in the manufacture of batches of product as required, e.g. for process development, stability studies or clinical trials

- Coordinates activities within Pharmaceutical Development and with analytical and manufacturing representatives to meet project results

- Works with the team to align and implement pre-formulation, formulation and process development activities including authoring or contributing to manufacturing batch records

- Identify and begin to interpret any problems in the execution of experimental processes and/or in results and communicates them to supervisor

- Proactively engage and seek assistance from other scientists to solve problems

- Maintains cleanliness in own work area and in communal work areas

- Anticipates/recognizes potential problems with equipment and/or supplies, and proposes/initiates action to solve or prevent problems

- Operates equipment for which is trained independently with due regard for GMP and Safety

- Demonstrates timely & reliable recording of laboratory data in Labware and other suitable systems in accordance with company policy and legal requirements.

- Performs data management tasks including recording results successfully and in compliance with departmental guidelines in a laboratory notebook or computer (e.g. tabulating and graphing results)

- Consults with supervisor when difficulties arise that cannot be readily resolved

- Prepares oral or written summaries of results with interpretation for project work

- Writes specific technical sections of internal and external reports with supervision

- Attends regular safety training and is fully aware of safety requirements for their laboratory/working environment

- Maintains accurate and complete safety records consistent with company policy and legal requirements

- Recognizes potential safety problems and takes action to resolve them

**Basic Requirements:**

- BS degree with 2-4 years of experience in an appropriate subject area

- Is technically proficient in a number of formulation/process development techniques.

- Has good knowledge of GMP and GLP requirements, SOPs and policies

- Has operational knowledge of routine laboratory/plant equipment

~~In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.~~

Working Conditions and Environment:

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements:

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

**Benefits:**

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued

Scientist, Formulations

We are uniting science, technology and talent to get ahead of disease together.
Our community guidelines: https://gsk.to/socialmedia

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

**Site Name: ** USA - Pennsylvania - Upper Providence, GSK HQ, UK – London – New Oxford Street, Zug House

**Posted Date: ** May 22 2026

At GSK, we unite science, technology and talent to get ahead of disease together. We prioritize research into vaccines and medicines across our four core therapeutic areas of infectious diseases, HIV, respiratory/immunology, and oncology. We also remain open to other opportunities where the science aligns with our strategic approach.

Do you have an entrepreneurial spirit, insatiable curiosity, broad pharma expertise, and a strong commitment to deploying insights to guide business strategy? If so, consider being a key partner in the growth of GSK Oncology as **Global Strategic Insights (GSI) Director.**

In this role, you will drive strategic insight generation that will define and shape Global Product Strategy for one of our Oncology brands, one which is a critical launch asset from the Anti-drug Conjugate (ADC) portfolio and the EMBOLD clinical development program. Working closely with the Global Product Strategy Commercialization Leader and a wide, cross-functional group of partners, you will:

- Lead insight generation to shape and drive commercial forecasts for business governance milestones, in close partnership with cross-functional teams

- Define, structure, plan, and commission global market research to proactively address key business questions and generate actionable and concise recommendations

- Leverage technology and innovation to increase efficiency and/or effectiveness in insight generation, while maintaining rigor and quality

- Develop robust forecast models ensuring seamless integration of market and customer insights into sound forecasts that contribute to investment planning decisions

- Partner with the Global Competitive Intelligence team to closely monitor the latest external developments, and translate these into concise and impactful recommendations

- Be a thought-partner for the cross-functional teams

~~This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:~~

- Lead multiple workstreams, and exert influence within cross-functional matrices

- Harness the latest research and analytical methodologies to drive a competitive edge for GSK

- Develop deep subject matter expertise in lead indication, tracking trends, current and evolving competitive landscapes, and generating long-term strategic outlooks

- Deliver well-integrated, actionable insights and ensure their strategic application to support global strategy, governance, and investment decisions

- Manage vendor relationships to achieve a mutually rewarding partnership while ensuring excellence in insight generation execution

- Leverage a wide range of tools and resources to identify opportunities, assess program potential, and provide guidance to optimize development plans

- Continue to build your ability to influence the planning and activities of cross-functional teams to help create alignment, clarity, and a clear sense of shared responsibility for the brands you work on.

**Why you?**

**Basic Qualifications**

~~We are looking for professionals with these required skills to achieve our goals:~~

- Bachelor’s Degree

- Strong track record of pharmaceutical industry experience, preferably encompassing both global and regional business analytics & insights roles

- Direct Oncology commercialization experience or relevant consulting experience

- Significant experience conducting market research, combined with forecasting expertise

**Preferred Qualifications**

~~If you have the following characteristics, it would be a plus:~~

- MBA, MS, or MA in business, marketing science, or science

- Demonstrated ability to apply data and analyses to drive high impact business decisions

- Ability to leverage and synthesize a broad range of information sources to develop insight and generate clear, actionable recommendations that impact/drive decision-making at a business unit level

- Demonstrated ability to influence senior commercial leadership and confidently defend informed recommendations, combined with strong communication and presentation skills

- Prior experience supporting product launch and/or business development opportunity assessment

- Agility, flexibility, and comfort with ambiguity

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

**Why GSK?**

**Uniting science, technology and talent to get ahead of disease together.**

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

**Important notice to Employment businesses/ Agencies**

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Director, Global Strategic Insights – Oncology

**Work Schedule**

**Other**

**Environmental Conditions**

Office

Join us as a Scientist!

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

**Essential Qualifications:**

-  Bachelor’s degree in Packaging Engineering, Packaging Science, Chemistry, Life Science, with 2-4 years’ experience in parenteral package development, primarily in pharmaceutical industry

-  Analytical and/or lab based experience in the pharmaceutical industry

Preferred Qualifications:

-  Knowledge of parenteral packaging materials, components, vendors, analytical equipment, and technologies.

-  Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

-  Knowledge of domestic and international packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc).

-  Knowledge of statistical analysis and Design of Experiments as they apply to packaging operations.

-  Ability to quickly establish relationships with internal and external stakeholders.

-  Strong time management / organizational skills.

-  Evidence of team working skills and flexibility.

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

**Work Summary:**

To provide packaging development analytical support in the UP, PA site.

The task list outlined below provides a comprehensive summary of the crucial work that needs to be carried out in the Steriles Packaging Development lab/team. This work is primarily aimed at offering support for a multitude of projects related to Steriles ViiV projects in development at GSK.

**Tasks:**

-  Perform timely execution of lab based analysis, including experiment write up to support sterile primary package selection, integrity, stability, and lifecycle for the coordination and testing of samples

-  Examples of analytical technique include extrusion force testing, stopper movement assessment, CCI capabilities including HeLD, Vacuum Decay, and headspace analysis

-  Be a practical expert in a packaging/analytical technique relevant to a primary pack presentation, capable of training others in the technique and application

-  Collaborate with the Lab Manager to maintain the License To Operate (LTO) status in the Lab – including equipment maintenance, documentation and coordination with vendors, management monitoring, and safety requirements

-  Maintain packaging lab component and lab inventory, including ordering, receiving, and organization of lab space to enable dynamic, flexible laboratory workspace

-  Prepare and communicate data summaries to relevant project team members

**Stretch Tasks:**

-  Writing work instructions, study protocol contribution

-  Authoring/revising component specifications

-  Supporting document and knowledge management

**Working Conditions and Environment:**

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

**Physical Requirements:**

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

**Why Join Us?**

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Scientist: Steriles Packaging Development

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