ZipRecruiter

Log In

1

Compendial Scientist Jobs (NOW HIRING)

MilliporeSigma

Principal Scientist

Carlsbad, CA

Develop and maintain SOPs, work instructions, and templates for compendial and non-compendial ... Train and mentor junior scientists, providing technical guidance and coaching. * Develop and review ...

Eurofins

Routine HPLC Scientist

Cambridge, MA · On-site

$26 - $38/hr

Eurofins Scientific is an international life sciences company, providing a unique range of ... Execute routine analytical assays using electrophoresis, chromatography, and compendial methods to ...

Merck Group

Principal Scientist

Carlsbad, CA · On-site

Develop and maintain SOPs, work instructions, and templates for compendial and non-compendial ... Train and mentor junior scientists, providing technical guidance and coaching. * Develop and review ...

Fresenius Kabi

Sr Scientist

Grand Island, NY · On-site

$73K - $103K/yr

Job Summary The Senior Scientist is responsible for the coordination and leadership of method transfer/method verification/co-validation of compendial and non-compendial analytical methods utilized ...

Freseniusglobal

Sr Scientist

Grand Island, NY · On-site

$73K - $103K/yr

Job Summary The Senior Scientist is responsible for the coordination and leadership of method transfer/method verification/co-validation of compendial and non-compendial analytical methods utilized ...

New

next page

Showing results 1-20

All JobsCompendial Scientist Jobs

Compendial Scientist information

See salary details

$57.5K

$68K

$129K

How much do compendial scientist jobs pay per year?

As of Jul 10, 2026, the average yearly pay for compendial scientist in the United States is $68,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $59,500.00 per year, depending on experience, location, and employer.

What is the difference between Compendial Scientist vs Quality Control Analyst?

AspectCompendial ScientistQuality Control Analyst
Required credentialsBachelor's degree in life sciences, certifications in GMP/GLPBachelor's degree in sciences, certifications in GMP/GLP
Work environmentLaboratories, regulatory agencies, pharmaceutical companiesLaboratories, pharmaceutical manufacturing facilities
Employer and industry usageUsed in regulatory compliance, ensuring products meet pharmacopeial standardsUsed in testing and analyzing raw materials and finished products

Compendial Scientists focus on ensuring products meet pharmacopeial standards and regulations, often working on documentation and compliance. Quality Control Analysts primarily perform testing and analysis of samples to verify product quality. Both roles require similar credentials and work environments, but their core responsibilities differ in scope and focus.

What are the key skills and qualifications needed to thrive as a Compendial Scientist, and why are they important?

To thrive as a Compendial Scientist, you need a strong background in analytical chemistry, regulatory compliance, and scientific documentation, typically supported by a degree in chemistry, pharmacy, or a related field. Familiarity with laboratory instrumentation (such as HPLC, GC, and spectroscopy), compendial standards (USP, EP, JP), and quality management systems is essential. Attention to detail, critical thinking, and effective communication help ensure accuracy and clear documentation of results. These skills and qualities are crucial to maintain product quality, meet regulatory requirements, and support successful audits in the pharmaceutical industry.

What are some common challenges faced by Compendial Scientists when ensuring compliance with evolving pharmacopeial standards?

Compendial Scientists often encounter the challenge of staying current with frequently updated pharmacopeial standards and ensuring that laboratory methods and documentation remain fully compliant. This requires constant monitoring of regulatory changes, rapid adaptation of procedures, and effective collaboration with quality assurance, regulatory affairs, and analytical development teams. Timely communication and robust project management skills are essential to implement changes without disrupting ongoing operations. Proactively engaging in cross-functional meetings and training sessions can help address these challenges and ensure seamless compliance.

What are Compendial Scientists?

Compendial Scientists are professionals who specialize in ensuring that pharmaceutical products comply with standards set by official compendia, such as the United States Pharmacopeia (USP) or the European Pharmacopoeia (Ph. Eur.). They review, interpret, and implement compendial requirements into a company's quality control processes and documentation. Their work often involves collaborating with regulatory agencies, staying current with changes in compendial standards, and participating in the development or revision of monographs and methods. Compendial Scientists play a critical role in maintaining product quality, safety, and regulatory compliance in the pharmaceutical industry.
More about Compendial Scientist jobs
What cities are hiring for Compendial Scientist jobs? Cities with the most Compendial Scientist job openings:
What states have the most Compendial Scientist jobs? States with the most job openings for Compendial Scientist jobs include:
What job categories do people searching Compendial Scientist jobs look for? The top searched job categories for Compendial Scientist jobs are:
Compendial Scientist jobs near you
Sr. Scientist II - Compendial Testing - 2nd Shift

Sr. Scientist II - Compendial Testing - 2nd Shift

Alcami Corporation

Morrisville, NC • On-site

$85K - $116K/yr

Full-time

Posted 28 days ago

Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Sr. Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this position, Titrations, CKF/KF, dissolution and/or CCIT based methodologies are commonly employed in the described compendial testing. Other key methodologies applied include: TLC, HPLC, GC, UV.
On-Site Expectations
  • 100% on-site position.
  • 2nd Shift: Monday - Friday, 3:00pm - 11:30pm.

Responsibilities
  • Combination of basic and advanced skills in multiple techniques: Titrations, assays (potencies, related substances), dissolution, moisture content, identification, CCIT and other various analytical techniques related to USP, EP, JP compendia.
  • A subject matter expert (SME) in few core techniques, such as CCIT, Titrations, HPLC, GC, Dissolution.
  • Achieves results by solving problems of a diverse scope by independently looking for solutions and reaching with minimal guidance.
  • Leads initiatives outside of standard work function.
  • Writes methods, test procedures, protocols and reports.
  • Able to do advanced troubleshooting of systems.
  • Independently performs/writes investigations and work with quality to complete.
  • Executes complex method development/validation/ verifications and routine testing with little to no assistance.
  • Actively seek to expand their working knowledge of routine instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Performs assigned tasks carefully and on schedule according to standard operating procedure and supervisor instructions.
  • Analyzes information for technical correctness and accuracy.
  • Complies with applicable GMPs, peer checks information and signs for GMP review. Brings aberrant information to the attention of supervisor.
  • Participates in company sponsored training and maintains current status of certifications and is a certified trainer on several advanced techniques. Actively conducts training for others and identifies potential training improvements or modernizations. Maintains a safe, clean, and organized work environment free of safety hazards.
  • Suggests and helps implement improvements for safety, work quality, and productivity.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Routinely provides results for client review and discusses results with clients directly.
  • Seeks to cultivate mentorship, build leadership skills and foster a culture of "Team First" by being a mentor for new hires and helping set them up for success in the company.
  • Other duties as assigned.

Qualifications
  • Bachelor's degree in Chemistry or a related field with with at least 10 years industry experience, a Master's degree with at least 6 years of experience, or a PhD with at least 4 years of experience is required.
  • Prior laboratory experience or work experience in Pharmaceutical, CDMO, or cGMP required.

Knowledge, Skills, and Abilities
  • Excellent verbal and written communication and documentation skills required.
  • Excellent detail orientation and organizational skills required.
  • Excellent problem-solving and basic trouble-shooting ability required.
  • Excellent knowledge of Laboratory equipment and safety required.
  • Excellent knowledge of Laboratory Documentation is required.
  • Strong knowledge of cGMP in a pharmaceutical or regulated environment required.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.

Travel Expectations
  • Up to 5% domestic travel.

Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

What Alcami employees say

Workplace

Get the full story on Breakroom

Apply