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Rtp Pharma Jobs (NOW HIRING)

IntelliPro Group Inc.

NC · On-site

$60/hr

... RTP Pharma Site. The focus of this position will be as a key leader for investigations and project implementation for Manufacturing Sciences using their technical expertise on fill/finish, visual ...

Biogen

NC · On-site

$127K - $170K/yr

Situated in RTP Pharma with matrixed global engagement, this role demands an established expert who can influence at all organizational levels, mentor and develop EHS leaders, and strategically ...

Randstad

Technical Writer

Durham, NC

$64 - $69/hr

... RTP Pharma Site. The focus of this position will be as a key leader for investigations and project implementation for Manufacturing Sciences using their technical expertise on fill/finish, visual ...

Genomics Ltd

Business Development Lead

Triangle, VA · On-site

Hybrid from our RTP office OR Fully Remote based on the East Coast The Mission: Why We Exist ... You'll identify, qualify, develop, and close opportunities across pharma and biotech - connecting ...

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How much do rtp pharma jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for rtp pharma in the United States is $26.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $36.30 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Rtp Pharma position, and why are they important?

To thrive as an RTP Pharma professional, you generally need a strong background in pharmaceutical sciences, regulatory compliance, and drug development processes, often supported by a relevant bachelor's or advanced degree. Familiarity with laboratory information management systems (LIMS), quality assurance protocols, and industry-specific certifications such as Good Manufacturing Practices (GMP) is highly valuable. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate effectively and ensure accurate documentation. These skills are vital to maintaining regulatory standards, advancing product development, and ensuring the safety and efficacy of pharmaceuticals.

What are the main responsibilities and typical work environment for an RTP Pharma professional?

RTP Pharma professionals are commonly involved in research, testing, and formulation of pharmaceutical products, ensuring compliance with regulatory standards and company protocols. The work environment often includes both laboratory settings and office-based tasks, with frequent collaboration across multidisciplinary teams such as research, quality assurance, and regulatory affairs. Daily responsibilities may include conducting experiments, analyzing data, preparing documentation, and participating in meetings to discuss project progress. Collaboration and adaptability are key, as projects are often driven by strict deadlines and evolving scientific challenges.

What is an RTP Pharma job?

An RTP Pharma job typically refers to a role in the pharmaceutical industry located in Research Triangle Park (RTP), North Carolina. RTP is a major hub for biotech and pharmaceutical companies, offering positions in research, development, manufacturing, and regulatory affairs. Job responsibilities vary but often include drug formulation, clinical trials, quality control, and compliance with industry regulations. Positions may be available for scientists, engineers, technicians, and regulatory specialists.

More about Rtp Pharma jobs
What are the most commonly searched types of Rtp Pharma jobs? The most popular types of Rtp Pharma jobs are:
What job categories do people searching Rtp Pharma jobs look for? The top searched job categories for Rtp Pharma jobs are:
Rtp Pharma jobs near you
Infographic showing various Rtp Pharma job openings in the United States as of June 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $55,272 per year, or $26.6 per hour.

Technical Writer - Life Science

IntelliPro Group Inc.

NC • On-site

$60/hr

Contractor

Posted 12 days ago

Job description

Job Title: Technical Writer
Duration: 06 months with possible extension
Office: Research Triangle Park, NC 27709
Pay rate: $60/hr. on W2
Job Summary:
  • As a member of Manufacturing Sciences, the Technical Writer will provide written documentation expertise to the clinical and commercial manufacturing campaigns run at the Parenteral Facility RTP Pharma Site. The focus of this position will be as a key leader for investigations and project implementation for Manufacturing Sciences using their technical expertise on fill/finish, visual inspection, and packaging.
  • The incumbent will be tasked with writing PPQ Protocols, PPQ Reports, data verification activities for confirmation of source data for reports, preliminary writing for sections of the filing. Creating the Master Sample Matrix (MSM) for Manufacturing personnel to be used for on the production floor activities.

Qualifications Required:
  • Life Science background with at least 5 years' experience.
  • Good communication and project management skills appropriate for leadership of tech transfer projects
  • Working knowledge in technical understanding of Parenteral Filling Operations (e.g. Filling Isolator, Lyophilizer, Visual Inspection) including transfer of such processes into full-scale drug product manufacturing facilities
  • Excels at working in a team environment
  • Comfortable analyzing scientific datasets/analytical skills with excellent written skills
  • Ability to work independently and support a large cross-functional group
  • Some knowledge of cGMP, FDA/EMA regulations, Process Performance Qualification, Continued Process Verification.

About Us:
Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.
IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.
Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

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