The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in can provide you with great development and a chance to see if we are the right company for your long-term goals.
Our company's Innovation, Quality and Strategic Execution is offering internships in the following area: Global Submissions Publishing (GSP). GSP is a high-performing team in our Company's Global Regulatory Affairs and Clinical Safety area responsible for publishing high-quality complex submission components, assembling, and delivering regulatory dossiers that advance patient access to the company's products in the global biopharmaceutical arena. The successful candidate will integrate into a team of professionals using MS Word, PDF, and technical aptitude to provide value in the end-to-end submission development process. The successful candidate will possess a capacity for applying critical thinking to contribute to innovation and efficiencies within the GSP team. The internship will incorporate overview and some support of document/submission publishing and will feature projects to support business operations. The internship will culminate with an opportunity to present achievements to various members of staff including senior management.
We are seeking candidates with excellent academic performance, communication skills, teamwork, and the ability to work in a multi-functional environment.
_Please note when applying for this position, if selected for an interview, the applicant must be prepared to submit letters of recommendation and a copy of his/her transcript. Applicant must indicate preferred location(s) when applying for this position in those cases where multiple locations are listed._
**Required Education and Skills:**
+ Candidates must be pursuing a minimum of a bachelor's degree in a related field with demonstrated interest/experience in in Business Admin, Business/Management, Computer Science, Communication Studies, Medical Science, or Pharmaceutical Science.
+ Candidates must be proficient in MS Office applications including Word and Outlook.
+ Candidates must be proficient working with Portable Document Format (PDF) files and familiar with PDF navigation using bookmarks and links.
+ Candidates must be available to work full-time for up to (12) weeks during the months of June - August 2021
**Preferred Experience and Skills:**
+ Candidates should have a fundamental understanding and interest in data collection with ability or interest to present metrics meaningfully.
+ Candidates should have a capacity for learning advanced features in MS Word, Excel, Adobe Acrobat, Spotfire, as well as other job specific software and applications.
+ Candidates should have experience working in fast-paced environment with rapid priority shifts.
+ Candidates should have a GPA of 3.0 or higher.
Our Regulatory Affairs team brings new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.
**Who We Are ...**
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world's biggest investors in Research & Development.
**What we look for ...**
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue **Inventing For Life, Impacting Lives** while **Inspiring Your Career Growth** .
**Residents of Colorado**
Click here (https://survey.sogosurvey.com/r/O2fDro) to request this role's pay range.
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/inst/1422$1533/rel-task/3001$14.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
**US and Puerto Rico Residents Only:**
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL [survey.sogosurvey.com]) if you need an accommodation during the application or hiring process.
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster (https://www.dol.gov/sites/dolgov/files/ofccp/regs/compliance/posters/pdf/eeopost.pdf)
EEOC GINA Supplement
OFCCP EEO Supplement (https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCP_EEO_Supplement_Final_JRF_QA_508c.pdf)
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
**Search Firm Representatives Please Read Carefully**
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Intern/Co-op (Fixed Term)
No Travel Required
**Flexible Work Arrangements:**
**Valid Driving License:**
**Number of Openings:**
**Requisition ID:** R76359